EP2177275A1 - Pump dispenser for the titration of pharmaceuticals - Google Patents

Pump dispenser for the titration of pharmaceuticals Download PDF

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Publication number
EP2177275A1
EP2177275A1 EP09013034A EP09013034A EP2177275A1 EP 2177275 A1 EP2177275 A1 EP 2177275A1 EP 09013034 A EP09013034 A EP 09013034A EP 09013034 A EP09013034 A EP 09013034A EP 2177275 A1 EP2177275 A1 EP 2177275A1
Authority
EP
European Patent Office
Prior art keywords
dosage
dispensing
kit according
pharmaceutical
base
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP09013034A
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German (de)
French (fr)
Inventor
Erhard Dr. Seiller
Karlheinz Zulauf
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merz Pharma GmbH and Co KGaA
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Merz Pharma GmbH and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Priority to EP09013034A priority Critical patent/EP2177275A1/en
Publication of EP2177275A1 publication Critical patent/EP2177275A1/en
Ceased legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05BSPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B11/00Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
    • B05B11/01Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
    • B05B11/10Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle
    • B05B11/1001Piston pumps

Definitions

  • the present invention relates to a pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage.
  • the present invention also relates to the use of said kit for treating a patient.
  • a desired dosage regime and/or a desired overall dosage cannot or should not be achieved in a single step but rather by means of incrementally increasing or decreasing the dosage from a certain predefined initial dosage to a certain predetermined final dosage and/or by means of dosing in intervals.
  • titration This increase or decrease or alternating of dosages involving at least two dosages that are different from each other.
  • the titration of solid tablets is known, for example by providing a tablet of a given dosage and further providing instructions to administer fractions or multiples of said one tablet.
  • Titration packages comprising different tablets of increasing dosages (for example 5 mg, 10 mg, 15 mg, 20 mg) are also known from the art (see, e.g., US 2006/0278557 ).
  • a titration package and method for enabling compliance with a regime of changing dosage of medication over a period of time is provided.
  • the solid formulation package includes a backing having an array of receivers with the array including a plurality of columns and a plurality of rows.
  • a plurality of sets of tablets are provided with each tablet in set having a common dose of medication and a different dose than a tablet of a different set.
  • a solid formulation may not be available or may be difficult to implement.
  • manufacturing and providing a large number of different tablets may be cumbersome and ineffective.
  • at least four different tablets each having a different composition need to be manufactured and packaged/provided separately.
  • a method of dosing liquids known in the art is a droplet dispenser.
  • small droplets are dispensed out of a bottle having a comparatively small orifice.
  • the volume of the droplet so dispensed is determined, within a certain margin of error, by the geometry of the orifice.
  • a large number of droplets needs to be dispensed and counted, for example 20 droplets.
  • multiples of a base-dosage would need to be dispensed rendering this system cumbersome and error-prone, for example for elderly and/or impaired patients.
  • one object of the present invention is to provide a means for delivering a liquid or paste-like pharmaceutical to a patient in need thereof that allows for a high degree of flexibility in regard to how many and which multiples of a base-dosage can be administered and that allows for easy and safe dispensing of different dosages even if the patient is potentially impaired, for example in regard to vision or in regard to memory.
  • Drawbacks and limitations posed by the prior art as discussed above should be avoided or minimized.
  • a pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage.
  • said pump dispenser comprises at least a pump head and dispensing is achieved by means of actuating said pump head of said pump dispenser.
  • said pump dispenser comprises at least one pump head and at least one reservoir attached thereto.
  • Pump heads are easy to operate and are made, in one embodiment, big enough and ergonomically suitable for operation by elderly patients, visually impaired patients and/or patients who are impaired in regard to motion control.
  • the pump head is of the "push-plunger'-type, i.e. comprises at least one plunger or piston or actuated pusher, i.e. actuator, and at least one sealed chamber in which a pressure can be built up by means of moving said plunger/piston/ actuator.
  • said pump dispenser comprises at least one hollow body with a chamber of a defined inner volume and a defined inner diameter.
  • said hollow body comprises a recess that has a diameter that is larger than said inner diameter of the chamber.
  • said pump dispenser additionally comprises at least one ball acting as a one-way valve and at least one piston that runs inside said hollow body.
  • the volume as defined by the chamber inside said hollow body of the dispenser head is more than 0.1 ml or more than 0.5 ml or more than 1 ml or more than 3 ml. In accordance with another embodiment, said volume ranges from 0.1 ml to 5.0 ml or from 0.3 ml to 3 ml or from 0.5 ml to 1 ml.
  • the spout of the pump dispenser i.e. the part of the pump head out of which the liquid or paste-like pharmaceutical is ultimately expelled is arcuate, i.e. has at least one portion that is substantially parallel to the horizontal plane and has at least one other portion that is inclined in at least a 45 degree angle relative to said horizontal plane.
  • the dispensing of the base-dosage is achieved by performing one stroke of an actuator or plunge or piston of the pump head.
  • one stroke means one single stroke.
  • said liquid or paste-like pharmaceutical comprises at least one NMDA receptor antagonist and/or at least one acetylcholinesterase inhibitor and/or at least one ⁇ 9 / ⁇ 10 nicotinic receptor antagonist.
  • said liquid or paste-like pharmaceutical comprises at least memantine and/or neramexane and/or pharmaceutically acceptable salts thereof such as memantine HCl or neramexane mesylate.
  • said titration scheme comprises at least one up-titration step, i.e. comprises the dispensing of at least two or at least three or at least four increasing integer multiples of said predetermined base-dosage, for example the dispensing of at least two increasing integers of the base-dosage with said integer starting at 1.
  • said titration scheme comprises the dispensing of at least two or at least three or at least four decreasing integer multiples of said predetermined base-dosage.
  • Such a titration scheme may be used for decreasing the dosage to a certain predetermined final dosage (such as for a maintenance therapy).
  • the scheme may comprise at first the dispensing of an integer multiple n 1 of a base-dosage and consecutively dispensing an integer multiple n 2 , wherein n 2 ⁇ n 1 .
  • said titration scheme comprises the dispensing of at least two or at least three or at least four alternating dosages that are different from each other.
  • Such a titration scheme may be used for alternating between certain predetermined dosages (such as for an interval therapy).
  • each of the at least two different dosages are dispensed at least twice.
  • an initial dosage may be administered for several consecutive days, including one week or more than a week, for example once daily for one week, before the next (different) dosage is administered, for example a higher or a lower or an alternating dosage, also for example once daily for one week.
  • the kit as described in any one of the aforementioned embodiments is used for the treatment of a patient.
  • "dispensing” means “actuating a pump dispenser”. This is achieved, in one embodiment, by means of actuating the pump head of the pump dispenser, for example by performing one complete or one incomplete stroke of the actuator or plunge or piston of the pump head.
  • “one” means “one single”.
  • predetermined base-dosage means one specific volume that is dispensed per (incomplete or complete) stroke, for example 0.25 ml or 0.3 ml or 0.5 ml or 1 ml or 2 ml or 3 ml or 5 ml. This volume is defined by the geometry of the pump dispenser, for example of the pump head and the volume of the hollow chamber formed therein. Said predetermined base-dosage cannot be adjusted or altered by the patient.
  • an incomplete stroke of the actuator or plunge or piston of the pump head may also be sufficient, as long as the amount of fluid dispensed per (incomplete) stroke is the same or similar.
  • titration occurs in at least two steps of administering consecutively increasing multiple integers of the base-dosage.
  • Such a titration regime is referred to as "up-titra-tion " and may be used, for example, for administering memantine as the active ingredient.
  • said integer is starting at 1, i.e. one time the base-dosage is administered, then two times the base-dosage etc.
  • titration occurs in at least two steps of administering consecutive decreasing multiple integers of a base-dosage.
  • the starting dosage may be 100 %, i.e. 4 times the base-dosage of 25 % while the following dosage is 75 %, i.e. 3 times the base-dosage of 25 %.
  • Such a titration regime is referred to as "maintenance therapy" and may be used, for example, for administering neramexane or pharmaceutically acceptable salts thereof.
  • titration occurs in at least three steps of administering consecutive multiple integers of the base-dosage.
  • said integer starts at 1 and the dosage increases (i.e. 1 time the base-dosage, 2 times the base-dosage, 3 times the base-dosage, ...), while in another embodiment, the integer starts at a number ⁇ 3 and the dosage decreases (i.e. 3 times the base-dosage, 2 times the base-dosage, 1 time the base-dosage).
  • titration occurs in at least four steps of administering consecutive multiple integers of the base-dosage with said integer starting at 1 (i.e. 1 time the base-dosage, 2 times the base-dosage, 3 times the base-dosage, 4 times the base-dosage or 4 times the base-dosage, then 3 times the base-dosage etc.), while in another embodiment, the integer starts at a number ⁇ 4 and the dosage correspondingly decreases.
  • titration occurs in intervals with a high dosage and a subsequent lower dosage followed again by said high dosage etc.
  • a practitioner prescribing the kit may devise individual titration schemes for individual patients while using one pump dispenser provided with one base-dosage that can therefore be manufactured and provided commercially at minimum operating expenses.
  • Liquid or paste-like pharmaceuticals according to the present invention may be in the form of a solution, a dispersion or an emulsion (micro- or nano-emulsions, self-emulsifying system, multiple emulsions) or in the form of a gel, paste, suspension (micro- or nano-suspension), hydrosol, liposome, mixed micells or in other forms of colloidal disperse systems such as drug loaded microparticles, nanocapsules or nanoparticles dispersed in a colloidal system or solution.
  • Paste-like masses may display a Newtonian or a non-Newtonian flow behaviour.
  • Active pharmaceutical ingredients that may be administered in accordance with such a titration scheme are or may be the following active ingredients in liquid or in paste-like form: uncompetitive channel blockers (e.g. NMDAr antabonists, e.g. amantadine, dextromethorphan, ibogaine, ketamine, phencyclidine, riluzole, memantine, neramexane), antagonists at ⁇ 9 / ⁇ 10 nicotinic receptors (e.g. neramexane), non-competitive antagonists (e.g. dizocilpine, aptiganel, remacimide), glycine antagonists (e.g.
  • NMDAr antabonists e.g. amantadine, dextromethorphan, ibogaine, ketamine, phencyclidine, riluzole, memantine, neramexane
  • ACPC 1-aminocyclopropanecarboxylic acid
  • competitive antagonists e.g. AP7 (2-amino-7-phosphonoheptanoic acid)
  • thrombolytics e.g. reteplase, tenecteplase, anistreplase, streptokinase, urokinase
  • anticoagulants e.g. heparin, warfarin, acenocoumarol, phenprocoumon, phenindione, argatroban, lepirudin, bivalirudin
  • antibiotics corticosteroids
  • antiplatelet agents e.g. aspirin, clopidogrel, ticlopidine, abciximab, eptifibatide, tirofiban, cilostazol
  • non-stereoidal anti-inflammatories e.g. salicylates (e.g.
  • arylalkanoic acids e.g. diclofenac, aceclofenac, acemetacin, bromfenac, etodolac, indometacin, nabumetone, sulindac, tometin
  • 2-Arylpropionic acids profens
  • ibuprofen carprofen, fenbufen, fenoporfen, flurbiprofen, ketoprofen, ketorolac, loxoprofen, naproxen, oxaprozin, tiaprofenic acid, suprofen), N-Arylanthranilic acids (fenamic acids) (e.g. mefenamic acid, meclofenamic acid), pyrazolidine derivates (e.g. phenylbutazone, azapropazone, metamizole, oxyphenbutazone, sulfinpyrazone), oxicams (e.g.
  • COX-2 inhibitors e.g. celecoxib, etoricoxib, lumiracoxib, parecoxib, rofecoxib, valdecoxib
  • sulphonanilides e.g. nimesulide
  • growth factors e.g.
  • TGF- ⁇ transforming growth factor beta
  • G-CSF granulocyte-colony stimulating factor
  • GM-CSF granulocyte-macrophage colony stimulating factor
  • NGF nerve growth factor
  • PDGF platelet derived growth factor
  • EPO erythropoietin
  • TPO thrombopoietin
  • GDF-9 growth differentiation factor-9
  • aFGF or FGF-1 acidic fibroblast growth factor
  • bFGF or FGF-2 basic fibroblast growth factor
  • EGF epidermal growth factor
  • HGF hepatocyte growth factor
  • immunosuppressant drugs e.g.
  • cyclosporine tacrolimus, prednisolone, azathioprine, sirolimus, mycopehnolate, glatiramer acetate
  • antineoplastic agents alkylating agents (e.g. cisplatin, carboplatin, oxaliplatin, mechlorethamine, cyclophosphamide, chlorambucil), anti-metabolites (e.g. azathioprine, mercaptopurine, pyrimidine), vinca alkaloids (e.g. vincristine, vinblastine, vinorelbine, vindesine), podophyllotoxin (e.g. etoposide, teniposide), taxanes (e.g.
  • paclitaxel paclitaxel
  • topoisomerase inhibitors e.g. amsacrine, etoposide, etoposide phosphate, teniposide, camptothecins such as irinotecan, topotecan
  • antitumor antibiotics e.g. dactinomycin
  • monoclonal antibodies e.g. trastuzumab, cetuximab, rituximab, bevacizumab
  • ACE-inhibitors e.g.
  • captopril zofenopril, enalapril, ramipril, quinapril, perindopril, lisinopril, benazepril, fosinopril
  • Acetylcholinesterase Inhibitors e.g. donepezil, rivastigmine, pyridostigmine, tetrahydroaminoacridine physostigmine, galantamine, tacrine, edrophonium, neostigmine
  • HMG-coA reductase inhibitors e.g.
  • atorvastatin cerivastatin, fluvastatin, lovastatin, pravastatin, simvastatin
  • beta-blockers e.g. alprenolol, carteolol, levobunolol, mepindolol, metipranolol, nadolol, oxprenolol, penbutolol, pindolol, propranolol, sotalol, timolol, acebutolol, atenolol, betaxolol, bisoprolol, esmolol, metoprolol, nebivolol, carvedilol, celiprolol, lavetalol, butaxamin), calcium channel blockers (e.g.
  • nimodipine amlodipine, felodipine, nicardipine, nifedipine, nisoldipine, nitrendipine, lacidipine, lercandipine
  • long acting nitrates e.g. isosorbide dinitrate and mononitrate, nitroglycerin
  • cholesterol-lowering agents e.g. bezafibrate, ciprofibrate, clofibrate, gemfibrozil, fenofibrate.
  • the kit comprising a liquid or paste-like pharmaceutical comprises at least one NMDA receptor antagonist.
  • NMDAr antagonists may be compositions comprising, as pharmaceutically active ingredients, memantine or neramexane or pharmaceutically acceptable salts thereof.
  • kits comprising a liquid or paste-like pharmaceutical comprising at least one acetylcholinesterase inhibitor (AchEI).
  • acetylcholinesterase inhibitors may be compositions comprising, among others, donepezil, rivastigmine, pyridostigmine, tetrahydroaminoacridine, physostigmine, galantamine, tacrine, edrophonium, neostigmine and pharmaceutically acceptable salts thereof.
  • the fluid, liquid or paste-like substance may include any other solvent, solute, additive, adjuvant or excipient that is pharmaceutically acceptable.
  • solvent(s) water and alcohol, or mixtures thereof, are used as solvent(s).
  • Pump dispensers for dispensing liquids, viscous or paste-like masses, for example soap, lotion or condiments are known form the art.
  • a simple-to-operate push plunger housed in a container is known, for example, from US 3 463 093 .
  • Another example of a general use dispensing unit is given in US 5 326 000 .
  • a dispenser or delivery apparatus for flowable media, particularly very viscous or gel-like media, specifically also comprising pharmaceuticals is disclosed in US 4 728 008 .
  • the pump dispenser comprises at least one pump head and at least one reservoir attached thereto.
  • the pump head is of the "push-plunger"-type, i.e. comprises at least one plunger or piston or actuated pusher (actuator) and at least one sealed chamber in which a pressure can be built up by means of moving said plunger/piston/actuator.
  • Dispensing by means of the "push-plunger"-principle is seen as particularly advantageous for operation of the dispenser by visually impaired patients or patients having coordination/motion control issues as is typical for some of the indications in accordance with the present invention, for example dementia, glaucoma, Alzheimer's disease etc.
  • Droplet dispensers for liquids as known from pharmaceutical applications employing measuring spoons and/or narrow spouts for "counting" droplets are much less suitable for these indications/applications than the pump dispenser and kit in accordance with the present invention.
  • the pump dispenser dispenses said predetermined base-dosage essentially independent of the actuation path, and/or irrespective of how far the pump head has been actuated.
  • the amount of dispensed fluid is independent of how far the pump head (or, more specifically, the plunger) has been actuated once a predetermined threshold of the actuation path has been passed.
  • said threshold is defined by a recess in a chamber of the pump head of the dispenser.
  • the pump head comprises at least one hollow body (15) with a chamber (19) of a given inner diameter d 15 .
  • This chamber contains the substance to be dispensed during the next cycle.
  • This hollow body (15) also comprises a recess (20) with a diameter larger than d 15 .
  • the hollow body furthermore comprises a conical seat and a second channel (22). This second channel is connected to a larger reservoir of the substance to be dispensed, i.e. the reservoir of the overall dispenser.
  • a ball (21) is located in a conical seat of hollow body (15). Said ball (21) acts as a one-way valve and may seal off the second channel (22). Inside the hollow body (15) runs a piston (17) with a hollow stem (18) and an elastic lip at the lower end of piston (17).
  • the hollow stem (18) comprises a first channel (27).
  • a first spring (24) is provided between piston (17) and a shoulder of the hollow body (15). Said first spring (24) drives the piston away from the above-discussed reservoir.
  • the hollow stem (18) has a compartment at its top to house the cone (28) and a second spring (29). This small compartment is open (35) to lead to any tube or applicator or spout for actually dispensing the fluid. Cone (28) is loaded by this second spring (29) and will close channel (27). Further details can be taken from Figure 1 .
  • the cycle of dispensing the substance and refilling chamber (19) can be achieved as follows. Initially, chamber (19) is filled with the pharmaceutical substance to be dispensed. Springs (24) and (29) are not fully expanded. The second and first channels (22) and (27) are closed. The dispensing cycle is started by pushing the stem (18) into the hollow body (15). Meanwhile, piston (17) is driven further into the hollow body (15) thus increasing the chamber pressure. At the same time, spring (24) is being compressed.
  • the second spring (29) yields to said chamber pressure.
  • This "yielding" can be adjusted (or "predetermined") by choosing an appropriate second spring (29).
  • the cone (28) opens the first channel (27).
  • the pharmaceutical substance now flows out of chamber (19) through first channel (27) and opening (35), driven by the chamber pressure.
  • the second spring (29) reaches the recess (20) the chamber pressure collapses.
  • the dose (volume) of the supplied substance is determined by the inner diameter d 15 of hollow body (15) and the distance covered by piston (17) before reaching the annular recess (20).
  • first spring (24) will push piston (17) upwards along the hollow body (15). On its way up the elastic lower lip of piston (17) will exit the annular recess (20) and reengage with the inner diameter of the chamber (19) thus sealing said chamber. Further travel of piston (17) causes the chamber pressure to drop further.
  • the reduced chamber pressure allows ball (21) to leave its conical seat, i.e. opens up the seal.
  • the reduced chamber pressure draws fresh liquid or paste from the large reservoir into chamber (19) until the shoulder of stem (18) makes contact with bar (52). This contact of stem (18) and the bar (52) ends the cycle of operation.
  • the pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical comprises at least one pump head comprising a hollow body with a chamber of a defined inner volume and a defined inner diameter, wherein the hollow body further comprises a recess that has a diameter that is larger than said inner diameter of the chamber.
  • the overall dispensed volume per stroke i.e. the volume of the predetermined base-dosage
  • the volume as defined by the chamber inside the hollow body of the dispenser head is more than 0.3 ml, more than 0.5 ml or more than 1 ml.
  • the concentration of the active ingredient in said predetermined dispensed volume is comparatively low, for example lower than 50 % (by volume), lower than 10 % or lower than 5 % or lower than 1 %.
  • concentration of the active ingredient in said predetermined dispensed volume is comparatively low, for example lower than 50 % (by volume), lower than 10 % or lower than 5 % or lower than 1 %.
  • 5 mg of active ingredient may be present in a base-dosage of 0.5 ml (resulting in a 1 % solution).
  • any possible variation in dispensed volume per successive stroke translates only into a small variation in dispensed active ingredient, i.e. in base-dosage.
  • Commonly used droplet bottles for dispensing liquid pharmaceuticals comprise a particularly narrow opening or spout through which only small droplets can be expelled. Due to the geometric constraint of the small opening and the action of surface tension, the volume of these small droplets is comparatively constant, albeit very small. In order to compensate for volume fluctuations and in order to achieve a final volume that can be reasonably administered, for example in a spoon, a large number of these small droplets needs to be dispensed in order to arrive at the one pre-described dosage, for example 20 droplets or 30 droplets.
  • This administration scheme has a couple of draw-backs, in particular the requirement to count a large number of droplets. Therefore, such an administration scheme is not suitable for patients that are physically and/or mentally impaired.
  • the presently described pump-dispenser is designed to have an easy-to-use actuation head (as known, for example, from everyday usage soap dispensers) while dispensing the required base-dosage in one stroke.
  • an easy-to-use actuation head as known, for example, from everyday usage soap dispensers
  • this may be achieved in the comparatively small number of two or three strokes (using a droplet-based dispenser as described above, for example the dispensing of two or three times 20 droplets would be required to achieve the same result).
  • the spout of the pump dispenser i.e. the part of the pump head out of which the liquid, viscous or paste-like pharmaceutical is ultimately expelled is arcuate, i.e. has at least one portion that is substantially parallel in the horizontal direction and has at least one portion that is inclined in at least a 45 degree angle relative to the horizontal plane.
  • This arcuate spout allows for a less spill-prone dispensing and is of particular advantage if the user of the dispenser is an older, handicapped or visually impaired patient.

Abstract

The present invention relates to a pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage. The present invention also relates to the use of such a kit for the treatment of a patient.

Description

    FIELD OF THE INVENTION
  • The present invention relates to a pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage.
  • The present invention also relates to the use of said kit for treating a patient.
  • BACKGROUND OF THE INVENTION
  • For certain pharmaceutical compositions, a desired dosage regime and/or a desired overall dosage cannot or should not be achieved in a single step but rather by means of incrementally increasing or decreasing the dosage from a certain predefined initial dosage to a certain predetermined final dosage and/or by means of dosing in intervals.
  • This increase or decrease or alternating of dosages involving at least two dosages that are different from each other is referred to as "titration" in the following.
  • In the prior art, the titration of solid tablets is known, for example by providing a tablet of a given dosage and further providing instructions to administer fractions or multiples of said one tablet.
  • Titration packages comprising different tablets of increasing dosages (for example 5 mg, 10 mg, 15 mg, 20 mg) are also known from the art (see, e.g., US 2006/0278557 ). Therein, a titration package and method for enabling compliance with a regime of changing dosage of medication over a period of time is provided. The solid formulation package includes a backing having an array of receivers with the array including a plurality of columns and a plurality of rows. A plurality of sets of tablets are provided with each tablet in set having a common dose of medication and a different dose than a tablet of a different set.
  • In some cases, however, a solid formulation may not be available or may be difficult to implement. Also, in case the titration scheme comprises a large number of different dosages, manufacturing and providing a large number of different tablets may be cumbersome and ineffective. For example, according to US 2006/0278557 , at least four different tablets each having a different composition need to be manufactured and packaged/provided separately.
  • A method of dosing liquids known in the art is a droplet dispenser. Therein, small droplets are dispensed out of a bottle having a comparatively small orifice. The volume of the droplet so dispensed is determined, within a certain margin of error, by the geometry of the orifice. In order to average fluctuations in the droplet volume, a large number of droplets needs to be dispensed and counted, for example 20 droplets. In order to achieve titration, multiples of a base-dosage would need to be dispensed rendering this system cumbersome and error-prone, for example for elderly and/or impaired patients.
  • OBJECTS OF THE INVENTION
  • Therefore, one object of the present invention is to provide a means for delivering a liquid or paste-like pharmaceutical to a patient in need thereof that allows for a high degree of flexibility in regard to how many and which multiples of a base-dosage can be administered and that allows for easy and safe dispensing of different dosages even if the patient is potentially impaired, for example in regard to vision or in regard to memory. Drawbacks and limitations posed by the prior art as discussed above should be avoided or minimized.
  • SUMMARY OF THE INVENTION
  • This object, among others, is solved by a pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage.
  • This object is also solved by the use of said kit for treating a patient.
  • In accordance with one embodiment of the present invention, said pump dispenser comprises at least a pump head and dispensing is achieved by means of actuating said pump head of said pump dispenser.
  • In accordance with another embodiment of the present invention, said pump dispenser comprises at least one pump head and at least one reservoir attached thereto. Pump heads are easy to operate and are made, in one embodiment, big enough and ergonomically suitable for operation by elderly patients, visually impaired patients and/or patients who are impaired in regard to motion control.
  • In accordance with another embodiment of the present invention, the pump head is of the "push-plunger'-type, i.e. comprises at least one plunger or piston or actuated pusher, i.e. actuator, and at least one sealed chamber in which a pressure can be built up by means of moving said plunger/piston/ actuator.
  • In accordance with another embodiment of the present invention said pump dispenser comprises at least one hollow body with a chamber of a defined inner volume and a defined inner diameter. In accordance with one embodiment of the present invention, said hollow body comprises a recess that has a diameter that is larger than said inner diameter of the chamber.
  • In accordance with another embodiment of the present invention, said pump dispenser additionally comprises at least one ball acting as a one-way valve and at least one piston that runs inside said hollow body.
  • In accordance with another embodiment of the present invention, the volume as defined by the chamber inside said hollow body of the dispenser head is more than 0.1 ml or more than 0.5 ml or more than 1 ml or more than 3 ml. In accordance with another embodiment, said volume ranges from 0.1 ml to 5.0 ml or from 0.3 ml to 3 ml or from 0.5 ml to 1 ml.
  • In accordance with yet another embodiment of the present invention, the spout of the pump dispenser, i.e. the part of the pump head out of which the liquid or paste-like pharmaceutical is ultimately expelled is arcuate, i.e. has at least one portion that is substantially parallel to the horizontal plane and has at least one other portion that is inclined in at least a 45 degree angle relative to said horizontal plane.
  • In accordance with another embodiment of the present invention, the dispensing of the base-dosage is achieved by performing one stroke of an actuator or plunge or piston of the pump head. Therein, "one stroke" means one single stroke.
  • In accordance with one embodiment of the present invention, said liquid or paste-like pharmaceutical comprises at least one NMDA receptor antagonist and/or at least one acetylcholinesterase inhibitor and/or at least one α910 nicotinic receptor antagonist.
  • In accordance with one embodiment of the present invention, said liquid or paste-like pharmaceutical comprises at least memantine and/or neramexane and/or pharmaceutically acceptable salts thereof such as memantine HCl or neramexane mesylate.
  • In accordance with one embodiment of the present invention, said titration scheme comprises at least one up-titration step, i.e. comprises the dispensing of at least two or at least three or at least four increasing integer multiples of said predetermined base-dosage, for example the dispensing of at least two increasing integers of the base-dosage with said integer starting at 1.
  • In accordance with one embodiment of the present invention, said titration scheme comprises the dispensing of at least two or at least three or at least four decreasing integer multiples of said predetermined base-dosage. Such a titration scheme may be used for decreasing the dosage to a certain predetermined final dosage (such as for a maintenance therapy). The scheme may comprise at first the dispensing of an integer multiple n1 of a base-dosage and consecutively dispensing an integer multiple n2, wherein n2 < n1.
  • In accordance with one embodiment of the present invention, said titration scheme comprises the dispensing of at least two or at least three or at least four alternating dosages that are different from each other. Such a titration scheme may be used for alternating between certain predetermined dosages (such as for an interval therapy). In one embodiment, each of the at least two different dosages are dispensed at least twice.
  • Any of the titration schemes is to be understood that an initial dosage may be administered for several consecutive days, including one week or more than a week, for example once daily for one week, before the next (different) dosage is administered, for example a higher or a lower or an alternating dosage, also for example once daily for one week.
  • In accordance with one embodiment of the present invention, the kit as described in any one of the aforementioned embodiments is used for the treatment of a patient.
  • DETAILED DESCRIPTION OF THE INVENTION
  • In accordance with one embodiment of the present invention, "dispensing" means "actuating a pump dispenser". This is achieved, in one embodiment, by means of actuating the pump head of the pump dispenser, for example by performing one complete or one incomplete stroke of the actuator or plunge or piston of the pump head. Therein, "one" means "one single".
  • In accordance with one embodiment of the present invention, "predetermined" base-dosage means one specific volume that is dispensed per (incomplete or complete) stroke, for example 0.25 ml or 0.3 ml or 0.5 ml or 1 ml or 2 ml or 3 ml or 5 ml. This volume is defined by the geometry of the pump dispenser, for example of the pump head and the volume of the hollow chamber formed therein. Said predetermined base-dosage cannot be adjusted or altered by the patient.
  • In accordance with one embodiment, an incomplete stroke of the actuator or plunge or piston of the pump head may also be sufficient, as long as the amount of fluid dispensed per (incomplete) stroke is the same or similar. Mechanisms ensuring such a repetitively stable modus of dispensing are described below, for example starting in paragraph [0046].
  • In one embodiment according to the present invention, titration occurs in at least two steps of administering consecutively increasing multiple integers of the base-dosage. Such a titration regime is referred to as "up-titra-tion" and may be used, for example, for administering memantine as the active ingredient. In a specific embodiment, said integer is starting at 1, i.e. one time the base-dosage is administered, then two times the base-dosage etc.
  • In another embodiment according to the present invention, titration occurs in at least two steps of administering consecutive decreasing multiple integers of a base-dosage. For example, the starting dosage may be 100 %, i.e. 4 times the base-dosage of 25 % while the following dosage is 75 %, i.e. 3 times the base-dosage of 25 %. Such a titration regime is referred to as "maintenance therapy" and may be used, for example, for administering neramexane or pharmaceutically acceptable salts thereof.
  • In a specific embodiment according to the present invention, titration occurs in at least three steps of administering consecutive multiple integers of the base-dosage. According to one embodiment, said integer starts at 1 and the dosage increases (i.e. 1 time the base-dosage, 2 times the base-dosage, 3 times the base-dosage, ...), while in another embodiment, the integer starts at a number ≥ 3 and the dosage decreases (i.e. 3 times the base-dosage, 2 times the base-dosage, 1 time the base-dosage).
  • In yet another embodiment according to the present invention, titration occurs in at least four steps of administering consecutive multiple integers of the base-dosage with said integer starting at 1 (i.e. 1 time the base-dosage, 2 times the base-dosage, 3 times the base-dosage, 4 times the base-dosage or 4 times the base-dosage, then 3 times the base-dosage etc.), while in another embodiment, the integer starts at a number ≥ 4 and the dosage correspondingly decreases.
  • In yet another embodiment of the invention, titration occurs in intervals with a high dosage and a subsequent lower dosage followed again by said high dosage etc.
  • As can be seen from the above, implementing various titration schemes by means of using one pump dispenser and simply varying the number of strokes is possible, while, at the same type working with only one base-dosage of the pharmaceutical composition (having a predetermined concentration in regard to the active ingredient).
  • ln accordance with the present invention, a practitioner prescribing the kit may devise individual titration schemes for individual patients while using one pump dispenser provided with one base-dosage that can therefore be manufactured and provided commercially at minimum operating expenses.
  • Liquid or paste-like pharmaceuticals according to the present invention may be in the form of a solution, a dispersion or an emulsion (micro- or nano-emulsions, self-emulsifying system, multiple emulsions) or in the form of a gel, paste, suspension (micro- or nano-suspension), hydrosol, liposome, mixed micells or in other forms of colloidal disperse systems such as drug loaded microparticles, nanocapsules or nanoparticles dispersed in a colloidal system or solution. Paste-like masses may display a Newtonian or a non-Newtonian flow behaviour.
  • Active pharmaceutical ingredients (APls) that may be administered in accordance with such a titration scheme are or may be the following active ingredients in liquid or in paste-like form: uncompetitive channel blockers (e.g. NMDAr antabonists, e.g. amantadine, dextromethorphan, ibogaine, ketamine, phencyclidine, riluzole, memantine, neramexane), antagonists at α910 nicotinic receptors (e.g. neramexane), non-competitive antagonists (e.g. dizocilpine, aptiganel, remacimide), glycine antagonists (e.g. 1-aminocyclopropanecarboxylic acid (ACPC), competitive antagonists (e.g. AP7 (2-amino-7-phosphonoheptanoic acid), thrombolytics (e.g. reteplase, tenecteplase, anistreplase, streptokinase, urokinase), anticoagulants (e.g. heparin, warfarin, acenocoumarol, phenprocoumon, phenindione, argatroban, lepirudin, bivalirudin), antibiotics, corticosteroids (e.g. beclomethasone, budesonide, betamethasone, ciclesonide, flunisolide, fluticasone, mometasone, refleponide, triamcinolone), antiplatelet agents (e.g. aspirin, clopidogrel, ticlopidine, abciximab, eptifibatide, tirofiban, cilostazol), non-stereoidal anti-inflammatories (NSAID) (e.g. salicylates (e.g. aspirin, amoxiprin, benorilate, choline magnesium salicylate, diflunisal, faislamine, methyl salicylate, magnesium salicylate, salicyl salicylate), arylalkanoic acids (e.g. diclofenac, aceclofenac, acemetacin, bromfenac, etodolac, indometacin, nabumetone, sulindac, tometin), 2-Arylpropionic acids (profens) (e.g. ibuprofen, carprofen, fenbufen, fenoporfen, flurbiprofen, ketoprofen, ketorolac, loxoprofen, naproxen, oxaprozin, tiaprofenic acid, suprofen), N-Arylanthranilic acids (fenamic acids) (e.g. mefenamic acid, meclofenamic acid), pyrazolidine derivates (e.g. phenylbutazone, azapropazone, metamizole, oxyphenbutazone, sulfinpyrazone), oxicams (e.g. piroxicam, lornoxicam, meloxicam, tenoxicam), COX-2 inhibitors (e.g. celecoxib, etoricoxib, lumiracoxib, parecoxib, rofecoxib, valdecoxib), sulphonanilides (e.g. nimesulide)), growth factors (e.g. transforming growth factor beta (TGF-β), granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), nerve growth factor (NGF), neurotrophins, platelet derived growth factor (PDGF), erythropoietin (EPO), thrombopoietin (TPO), myostatin (GDF-8), growth differentiation factor-9 (GDF9), acidic fibroblast growth factor (aFGF or FGF-1), basic fibroblast growth factor (bFGF or FGF-2), epidermal growth factor (EGF), hepatocyte growth factor (HGF)), immunosuppressant drugs (e.g. cyclosporine, tacrolimus, prednisolone, azathioprine, sirolimus, mycopehnolate, glatiramer acetate), antineoplastic agents (alkylating agents (e.g. cisplatin, carboplatin, oxaliplatin, mechlorethamine, cyclophosphamide, chlorambucil), anti-metabolites (e.g. azathioprine, mercaptopurine, pyrimidine), vinca alkaloids (e.g. vincristine, vinblastine, vinorelbine, vindesine), podophyllotoxin (e.g. etoposide, teniposide), taxanes (e.g. paclitaxel), topoisomerase inhibitors (e.g. amsacrine, etoposide, etoposide phosphate, teniposide, camptothecins such as irinotecan, topotecan), antitumor antibiotics (e.g. dactinomycin), monoclonal antibodies (e.g. trastuzumab, cetuximab, rituximab, bevacizumab)), ACE-inhibitors (e.g. captopril, zofenopril, enalapril, ramipril, quinapril, perindopril, lisinopril, benazepril, fosinopril), Acetylcholinesterase Inhibitors (e.g. donepezil, rivastigmine, pyridostigmine, tetrahydroaminoacridine physostigmine, galantamine, tacrine, edrophonium, neostigmine), HMG-coA reductase inhibitors (e.g. atorvastatin, cerivastatin, fluvastatin, lovastatin, pravastatin, simvastatin), beta-blockers (e.g. alprenolol, carteolol, levobunolol, mepindolol, metipranolol, nadolol, oxprenolol, penbutolol, pindolol, propranolol, sotalol, timolol, acebutolol, atenolol, betaxolol, bisoprolol, esmolol, metoprolol, nebivolol, carvedilol, celiprolol, lavetalol, butaxamin), calcium channel blockers (e.g. verapamil, gallopamil, diltiazem, nimodipine, amlodipine, felodipine, nicardipine, nifedipine, nisoldipine, nitrendipine, lacidipine, lercandipine), long acting nitrates (e.g. isosorbide dinitrate and mononitrate, nitroglycerin) or cholesterol-lowering agents (e.g. bezafibrate, ciprofibrate, clofibrate, gemfibrozil, fenofibrate).
  • According to one embodiment of the present invention, the kit comprising a liquid or paste-like pharmaceutical comprises at least one NMDA receptor antagonist. Such NMDAr antagonists may be compositions comprising, as pharmaceutically active ingredients, memantine or neramexane or pharmaceutically acceptable salts thereof.
  • Another embodiment according to the present invention relates to a kit comprising a liquid or paste-like pharmaceutical comprising at least one acetylcholinesterase inhibitor (AchEI). Such acetylcholinesterase inhibitors may be compositions comprising, among others, donepezil, rivastigmine, pyridostigmine, tetrahydroaminoacridine, physostigmine, galantamine, tacrine, edrophonium, neostigmine and pharmaceutically acceptable salts thereof.
  • In accordance with the present invention, no restrictions are made in regard to the composition of the fluid, liquid or paste-like substance that is being dispensed, other than that the fluid, liquid or paste-like substance must comprise at least one pharmaceutically active ingredient. Otherwise, the fluid, liquid or paste-like substance may include any other solvent, solute, additive, adjuvant or excipient that is pharmaceutically acceptable. According to one embodiment water and alcohol, or mixtures thereof, are used as solvent(s).
  • Pump dispensers for dispensing liquids, viscous or paste-like masses, for example soap, lotion or condiments are known form the art. A simple-to-operate push plunger housed in a container is known, for example, from US 3 463 093 . Another example of a general use dispensing unit is given in US 5 326 000 . A dispenser or delivery apparatus for flowable media, particularly very viscous or gel-like media, specifically also comprising pharmaceuticals is disclosed in US 4 728 008 .
  • In accordance with one embodiment of the present invention, the pump dispenser comprises at least one pump head and at least one reservoir attached thereto.
  • According to one embodiment of the present invention, the pump head is of the "push-plunger"-type, i.e. comprises at least one plunger or piston or actuated pusher (actuator) and at least one sealed chamber in which a pressure can be built up by means of moving said plunger/piston/actuator.
  • Dispensing by means of the "push-plunger"-principle is seen as particularly advantageous for operation of the dispenser by visually impaired patients or patients having coordination/motion control issues as is typical for some of the indications in accordance with the present invention, for example dementia, glaucoma, Alzheimer's disease etc. Droplet dispensers for liquids as known from pharmaceutical applications employing measuring spoons and/or narrow spouts for "counting" droplets are much less suitable for these indications/applications than the pump dispenser and kit in accordance with the present invention.
  • In one embodiment according to the present invention, the pump dispenser dispenses said predetermined base-dosage essentially independent of the actuation path, and/or irrespective of how far the pump head has been actuated. In one embodiment, the amount of dispensed fluid is independent of how far the pump head (or, more specifically, the plunger) has been actuated once a predetermined threshold of the actuation path has been passed.
  • In accordance with one embodiment of the present invention said threshold is defined by a recess in a chamber of the pump head of the dispenser.
  • There are no restrictions in regard to the specific mechanic design for achieving this dosing of one specific and predetermined base-dosage as long as the same or at least a sufficiently similar dosage is provided per at least partially executed stroke.
  • One possible technical realization for achieving a predetermined and reproducible dosage with one complete or one partially incomplete stroke is described in the following and illustrated by Figure 1 showing an exemplary pump head / dosage head in accordance with the afore-described embodiment of the present invention.
  • The pump head comprises at least one hollow body (15) with a chamber (19) of a given inner diameter d15. This chamber contains the substance to be dispensed during the next cycle. This hollow body (15) also comprises a recess (20) with a diameter larger than d15. The hollow body furthermore comprises a conical seat and a second channel (22). This second channel is connected to a larger reservoir of the substance to be dispensed, i.e. the reservoir of the overall dispenser.
  • A ball (21) is located in a conical seat of hollow body (15). Said ball (21) acts as a one-way valve and may seal off the second channel (22). Inside the hollow body (15) runs a piston (17) with a hollow stem (18) and an elastic lip at the lower end of piston (17). The hollow stem (18) comprises a first channel (27). A first spring (24) is provided between piston (17) and a shoulder of the hollow body (15). Said first spring (24) drives the piston away from the above-discussed reservoir. The hollow stem (18) has a compartment at its top to house the cone (28) and a second spring (29). This small compartment is open (35) to lead to any tube or applicator or spout for actually dispensing the fluid. Cone (28) is loaded by this second spring (29) and will close channel (27). Further details can be taken from Figure 1.
  • In the following, one mode of operation of this unit is explained. The cycle of dispensing the substance and refilling chamber (19) can be achieved as follows. Initially, chamber (19) is filled with the pharmaceutical substance to be dispensed. Springs (24) and (29) are not fully expanded. The second and first channels (22) and (27) are closed. The dispensing cycle is started by pushing the stem (18) into the hollow body (15). Meanwhile, piston (17) is driven further into the hollow body (15) thus increasing the chamber pressure. At the same time, spring (24) is being compressed.
  • At a predetermined chamber pressure, the second spring (29) yields to said chamber pressure. This "yielding" can be adjusted (or "predetermined") by choosing an appropriate second spring (29). Coincidentally with the yielding of the second spring (29), the cone (28) opens the first channel (27). The pharmaceutical substance now flows out of chamber (19) through first channel (27) and opening (35), driven by the chamber pressure. Once the elastic lower lip of piston (17) reaches the recess (20) the chamber pressure collapses. This causes the second spring (29) to reposition cone (28) thus closing channel (27). This ends the dispensing step, irrespective of how the pump head is further actuated and/or how the plunger/piston is retracted. The dose (volume) of the supplied substance is determined by the inner diameter d15 of hollow body (15) and the distance covered by piston (17) before reaching the annular recess (20).
  • Once the hollow stem (18) is released, first spring (24) will push piston (17) upwards along the hollow body (15). On its way up the elastic lower lip of piston (17) will exit the annular recess (20) and reengage with the inner diameter of the chamber (19) thus sealing said chamber. Further travel of piston (17) causes the chamber pressure to drop further. The reduced chamber pressure allows ball (21) to leave its conical seat, i.e. opens up the seal. The reduced chamber pressure draws fresh liquid or paste from the large reservoir into chamber (19) until the shoulder of stem (18) makes contact with bar (52). This contact of stem (18) and the bar (52) ends the cycle of operation.
  • Therefore, in one embodiment of the present invention, the pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical comprises at least one pump head comprising a hollow body with a chamber of a defined inner volume and a defined inner diameter, wherein the hollow body further comprises a recess that has a diameter that is larger than said inner diameter of the chamber.
  • While this mechanism is given as one example of how a predetermined amount of fluid can be dispensed with a high degree of reproducibility, this mechanism is only meant to serve as an example of the overall principle. The person skilled in the art readily knows of other mechanisms working in the same or in a similar manner.
  • In one embodiment according to the present invention and in order to mitigate any potential (small) error in reproducibility in regard to the absolute volume dispensed (for example an error of a fraction of a millilitre), the overall dispensed volume per stroke (i.e. the volume of the predetermined base-dosage) is comparatively large, for example more than0.3 ml per stroke, more than 0.5 ml per stroke or more than 1 ml per stroke. As a consequence, in one embodiment according to the present invention, the volume as defined by the chamber inside the hollow body of the dispenser head is more than 0.3 ml, more than 0.5 ml or more than 1 ml.
  • In one embodiment according to the present invention, while the volume dispensed per stroke is comparatively high, the concentration of the active ingredient in said predetermined dispensed volume is comparatively low, for example lower than 50 % (by volume), lower than 10 % or lower than 5 % or lower than 1 %. For example, 5 mg of active ingredient may be present in a base-dosage of 0.5 ml (resulting in a 1 % solution).
  • By means of dispensing a comparatively large volume with a comparatively low concentration of active ingredient(s), any possible variation in dispensed volume per successive stroke translates only into a small variation in dispensed active ingredient, i.e. in base-dosage.
  • Commonly used droplet bottles for dispensing liquid pharmaceuticals comprise a particularly narrow opening or spout through which only small droplets can be expelled. Due to the geometric constraint of the small opening and the action of surface tension, the volume of these small droplets is comparatively constant, albeit very small. In order to compensate for volume fluctuations and in order to achieve a final volume that can be reasonably administered, for example in a spoon, a large number of these small droplets needs to be dispensed in order to arrive at the one pre-described dosage, for example 20 droplets or 30 droplets. This administration scheme has a couple of draw-backs, in particular the requirement to count a large number of droplets. Therefore, such an administration scheme is not suitable for patients that are physically and/or mentally impaired. By contrast, the presently described pump-dispenser is designed to have an easy-to-use actuation head (as known, for example, from everyday usage soap dispensers) while dispensing the required base-dosage in one stroke. For example in a titration scheme requiring the administration of multiples of a base-dosage, for example two and three times the base-dosage, this may be achieved in the comparatively small number of two or three strokes (using a droplet-based dispenser as described above, for example the dispensing of two or three times 20 droplets would be required to achieve the same result).
  • In one embodiment according to the present invention, the spout of the pump dispenser, i.e. the part of the pump head out of which the liquid, viscous or paste-like pharmaceutical is ultimately expelled is arcuate, i.e. has at least one portion that is substantially parallel in the horizontal direction and has at least one portion that is inclined in at least a 45 degree angle relative to the horizontal plane. This arcuate spout allows for a less spill-prone dispensing and is of particular advantage if the user of the dispenser is an older, handicapped or visually impaired patient.

Claims (16)

  1. Pharmaceutical kit comprising (i) a pump dispenser for dispensing multiples of a predetermined base-dosage of a liquid or paste-like pharmaceutical (ii) said liquid or paste-like pharmaceutical contained in said pump dispenser and (iii) instructions for implementing a predetermined titration scheme, wherein said titration scheme comprises the dispensing of at least two different integer multiples of said predetermined base-dosage.
  2. Kit according to claim 1, wherein said pump dispenser comprises at least a pump head and dispensing is achieved by means of actuating said pump head of said pump dispenser.
  3. Kit according to claim 1 or 2, wherein said pump dispenser comprises at least one pump head and at least one reservoir attached thereto and wherein the pump head comprises at least one plunger or piston or actuated pusher, i.e. actuator, and at least one sealed chamber in which a pressure can be built up by means of moving said plunger/piston/ actuator.
  4. Kit according to any one of the preceding claims, wherein said pump dispenser comprises at least one hollow body with a chamber of a defined inner volume and a defined inner diameter, wherein said hollow body comprises a recess that has a diameter that is larger than said inner diameter of the chamber.
  5. Kit according to claim 4, wherein the pump dispenser additionally comprises at least one ball acting as a one-way valve and at least one piston that runs inside the hollow body.
  6. Kit according claim 4, wherein the volume as defined by the chamber inside the hollow body of the dispenser head is more than 0.1 ml, more than 0.3 ml or ranges from 0.3 to 3 ml.
  7. Kit according to any one of the preceding claims, wherein the spout of the pump dispenser, i.e. the part of the pump head out of which the liquid or paste-like pharmaceutical is ultimately expelled has at least one portion that is substantially parallel to the horizontal plane and has at least one other portion that is inclined in at least a 45 degree angle relative to said horizontal plane.
  8. Kit according to any one of the preceding claims, wherein said dispensing of the base-dosage is achieved by performing one stroke of an actuator or plunge or piston of the pump head.
  9. Kit according to any one of preceding claims, wherein said liquid or paste-like pharmaceutical comprises at least one NMDA receptor antagonist and/or at least one acetylcholinesterase inhibitor and/or at least one α910 nicotinic receptor antagonist.
  10. Kit according to claim 9, wherein the liquid or paste-like pharmaceutical comprises at least memantine and/or neramexane and/or pharmaceutically acceptable salts thereof.
  11. Kit according to any one of the preceding claims, wherein said titration scheme comprises the dispensing of at least two or at least three or at least four increasing integer multiples of said predetermined base-dosage.
  12. Kit according to claim 11, wherein said titration scheme comprises the dispensing of at least two increasing integers of the base-dosage with said integer starting at 1.
  13. Kit according to any one of the preceding claims, wherein said titration scheme comprises the dispensing of at least two or at least three or at least four decreasing integer multiples of said predetermined base-dosage.
  14. Kit according to claim 13, wherein the titration comprises at first the dispensing of an integer multiple n1 of a base-dosage and consecutively the dispensing of an integer multiple n2, wherein n2 < n1 and n1,n2 being > 1.
  15. Kit according to any one of the preceding claims, wherein said titration scheme comprises an interval therapy, i.e. comprises the dispensing of at least two or at least three or at least four alternating different dosages.
  16. Use of the kit according to any one of claims 1 to 15 for the treatment of a patient.
EP09013034A 2008-10-16 2009-10-15 Pump dispenser for the titration of pharmaceuticals Ceased EP2177275A1 (en)

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US19631308P 2008-10-16 2008-10-16
EP08018154 2008-10-16
EP09013034A EP2177275A1 (en) 2008-10-16 2009-10-15 Pump dispenser for the titration of pharmaceuticals

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Citations (11)

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US3463093A (en) 1967-01-17 1969-08-26 Erich Pfeiffer Kg Metallwarenf Simply operating push plunger pump housed in a container
US4565302A (en) * 1983-01-22 1986-01-21 Ing. Erich Pfeiffer Gmbh & Co. Kg Actuatable dosing mechanism
US4728008A (en) 1985-08-27 1988-03-01 Ing. Erich Pfeiffer Gmbh & Co. Kg Dispenser for flowable media
US5326000A (en) 1991-03-16 1994-07-05 Ing. Erich Pfeiffer Gmbh & Co. Kg Medium dispenser with mounting support for optional secondary dispensing unit
US5918568A (en) * 1996-08-26 1999-07-06 Pharmalett Denmark A/S Method of medicating and individualizing treatment shampoo for dermatological disturbances of companion animals
US20020066752A1 (en) * 2000-10-16 2002-06-06 Stefan Ritsche Dispenser and method for discharging media
US6605060B1 (en) * 1995-06-07 2003-08-12 O'neil Alexander George Brian Patient controlled drug delivery device
US20040050858A1 (en) * 2002-07-13 2004-03-18 Aero Pump Gmbh Double-acting pump for ejecting a product from a container
US20040135002A1 (en) * 2001-04-30 2004-07-15 Klaus-Dieter Beller Device for the spraying of fluids
US20060278557A1 (en) 2003-07-16 2006-12-14 Firestone Bruce A Memantine titration/compliance dosage forms
US20070275145A1 (en) * 2006-05-26 2007-11-29 Catani Steven J Method of delivering a high intensity sweetener to a liquid foodstuff

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3463093A (en) 1967-01-17 1969-08-26 Erich Pfeiffer Kg Metallwarenf Simply operating push plunger pump housed in a container
US4565302A (en) * 1983-01-22 1986-01-21 Ing. Erich Pfeiffer Gmbh & Co. Kg Actuatable dosing mechanism
US4728008A (en) 1985-08-27 1988-03-01 Ing. Erich Pfeiffer Gmbh & Co. Kg Dispenser for flowable media
US5326000A (en) 1991-03-16 1994-07-05 Ing. Erich Pfeiffer Gmbh & Co. Kg Medium dispenser with mounting support for optional secondary dispensing unit
US6605060B1 (en) * 1995-06-07 2003-08-12 O'neil Alexander George Brian Patient controlled drug delivery device
US5918568A (en) * 1996-08-26 1999-07-06 Pharmalett Denmark A/S Method of medicating and individualizing treatment shampoo for dermatological disturbances of companion animals
US20020066752A1 (en) * 2000-10-16 2002-06-06 Stefan Ritsche Dispenser and method for discharging media
US20040135002A1 (en) * 2001-04-30 2004-07-15 Klaus-Dieter Beller Device for the spraying of fluids
US20040050858A1 (en) * 2002-07-13 2004-03-18 Aero Pump Gmbh Double-acting pump for ejecting a product from a container
US20060278557A1 (en) 2003-07-16 2006-12-14 Firestone Bruce A Memantine titration/compliance dosage forms
US20070275145A1 (en) * 2006-05-26 2007-11-29 Catani Steven J Method of delivering a high intensity sweetener to a liquid foodstuff

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