DK2723439T3 - APPLICATION SYSTEM FOR APPLICATION OF A VISCULAR LIQUID ON HUMAN SKIN - Google Patents

Description

DESCRIPTION

[0001] The invention relates to an applicator system for applying a viscous liquid, in particular a transdermal pharmaceutical formulation, to the human skin comprising, a metering dispenser in turn comprising a container holding the viscous liquid and a pump for metering the liquid and an applicator detachably connected to the dispenser and comprising an application surface for receiving a metered amount (dose) ofthe liquid from the dispenser.

[0002] As explained in WO 2008/083423, topical liquids such as sunscreens or medicated liquids have previously been provided in squeezable containers or in containers with a finger operated pump whereby a portion of the liquid is deposited on the treatment surface or on a free hand for subsequent application to the treatment surface. In either case the liquid is spread over the treatment surface with the free hand which results in the liquid being applied to a surface other than the treatment surface. It is not always acceptable for the free hand to be treated with a medicated liquid as the volume dispensed from the container may be a prescribed dose. This is particularly the case where the liquid is intended to have a therapeutic effect at the prescribed dose.

[0003] It is often desirable to provide an implement which temporarily retains the liquid for application to the treatment surface. Implements tend to suffer from the tension between temporarily retaining the liquid and having to release the liquid onto the treatment surface. Implements such as brushes and sponges are effective in spreading the liquid over the treatment surface however they tend to retain a volume of residual liquid after the application of the implement to the treatment surface. The retained volume may vary from application to application and as such it is difficult to accurately apply a metered dose to a treatment surface using an implement such as a brush or sponge.

[0004] In WO 2008/083423, it is considered desirable to provide an implement that is capable of applying a liquid to a treatment surface while minimising retention of residual liquid, and also an implement that was easy to clean after use. In WO 2008/083423, there is provided an implement for applying a volume of liquid to a treatment surface including a support means onto which is mounted a receptacle defining a reservoir space which receives the volume of liquid, the receptacle having a base and a wall. The wall is substantially transverse to the base and has a working surface that is used to spread the liquid over the treatment surface. At least the wall is resiliently deformable so in use the working surface maintains contact with the treatment surface when spreading the liquid.

[0005] The applicator according to WO 2008/083423 is intended for applying low viscosity liquids, typically having a viscosity of "less than 300 centipoise and often about 150 centipoise".

[0006] It is an object of the present invention to provide an improved applicator system that allows accurate transfer of metered amounts of viscous liquids, e.g. gels, from the application surface to the skin.

[0007] To this end, in the applicator system according to the present invention, the application surface is convex and continuous and a hygiene cap is provided to cover the application surface.

[0008] In an embodiment, the application surface comprises no apertures or porous regions for metering the liquid to the surface from a supply within.

[0009] In a further embodiment, the application surface is rigid, i.e. non-deformable. More specifically, it is preferred that the material forming the surface has a Young's modulus of at least 1.5 GPa, preferably in a range from 2 to 4 GPa.

[0010] The application surface according to the present invention enables substantially complete transfer ofthe metered viscous liquid to the skin.

[0011] To further enhance transfer ofthe viscous liquid from the application surface to the skin, it is preferred that the application surface is smooth, preferably having a texture of stage 21 (measured in accordance with the VDI 3400 standard) or smoother.

[0012] The applicator according to the present invention can be used in combination with standard metering pumps, made in large quantities and thus providing good accuracy at relatively low costs. As the applicator surface provides substantially complete transfer of metered viscous liquid, the accuracy ofthe metering pump is extended to actual application.

[0013] In an embodiment, the dispenser has a metering accuracy of +/- 15%, preferably +/-10% of the set amount and/or is configured to provide a metered amount per dispense in a range from 0.5 to 2.5 ml. In one embodiment, the dispenser provides a metered amount per dispense in a range from 1.0 to 2.0 ml. In another embodiment, the dispenser provides a metered amount per dispense of 1.25 ml.

[0014] In a particularly practical embodiment, the applicator doubles as a cap for the dispenser and/or comprises a sleeve to receive and secure the dispenser, e.g. through clamping or by means of a screwed or bayonet connection.

[0015] In a further embodiment, the applicator has a total length of at least 6.5 centimeters, preferably at least 9 centimeters, and is preferably not longer than 15 centimeters and/or at least 50% of the length of the applicator is suitable as a grip. Thus, the applicator is sufficiently long to envelop and secure the dispenser and to allow effective and comfortable handling by a user. In one embodiment, the applicator has a total length of about 12 centimeters.

[0016] In another embodiment, the dispenser contains a viscous liquid having a viscosity of at least 3000 centipoise (at 25°C), preferably in a range from 5000 to 50000 centipoise, more preferably in a range from 17000 to 24000 centipoise. Thus, the viscous liquid, e.g. a gel, will adhere to the application surface, reducing the risk of gel metered onto the surface falling off e.g. as a result of movements by the user.

[0017] The system is especially suitable for applying a viscous liquid comprising testosterone or a derivative thereof.

[0018] When referring to testosterone, it should be understood to refer to the androgen steroidal hormone 17-P-hydroxyandrostenone also named (8R, 9S, 10R, 13S, 14S, 17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17 dodecahydrocyclopenta[a]phenanthren-3-one (CAS Registry Number 58-22-0).

[0019] Examples of other androgens which may be administered with the applicator system of the invention include, but are not limited to, any esters of testosterone (such as testosterone enanthate, propionate, cypionate, phenylacetate, acetate, isobutyrate, buciclate, heptanoate, decanoate, undecanoate, caprate and isocaprate esters), 4-dihydrotestosterone, and any pharmaceutically acceptable derivatives of testosterone such as for example methyl testosterone, testolactone, oxymethoIone and fluoxymesterone. These androgens may be used alone or in combinations of two or more thereof.

[0020] The system is also suitable for applying transdermal pharmaceutical formulations comprising at least one active agent and a solvent system present in an amount sufficient to solubilize the at least one active ingredient.

[0021] In one embodiment, the viscous liquid is a formulation comprising an active agent and a solvent system as specified in US 7,198,801. In a specific embodiment, the active agent in the formulation is testosterone or a derivative thereof.

[0022] Examples of preferred testosterone formulations to be administered with an applicator ofthe invention are specified in PCT application no. PCT/EP2012/050695.

[0023] In one embodiment, the viscous liquid is a formulation comprising a C2-C4 alkanol in an amount between about 5 - 50%wt, polyalcohol in an amount between about 1 - 30%wt, monoalkyl ether of diethylene glycol in an amount between about 0.2 - 25%wt, gelling agent in an amount between about 0.05 - 4%wt, neutralizing agent in an amount between about 0.05-1 %wt, and chelating agent in an amount between about 0.001-5.0%wt.

[0024] Unless expressly specified otherwise, the term "comprising" is used in the context of the present application to indicate that further members may optionally be present in addition to the members explicitly mentioned. It is, however, contemplated as a specific embodiment of the present invention that the term "comprising" encompasses the possibility of no further members being present. In other words, for the purpose of this embodiment, "comprising" is to be understood as having the meaning of "consisting of".

[0025] The following detailed description discloses specific and/or preferred variants of the individual features of the invention. The present invention also contemplates as particularly preferred embodiments those embodiments, which are generated by combining two or more of the specific and/or preferred variants described for two or more of the features of the present invention.

[0026] Unless expressly specified otherwise, all indications of relative amounts in the present application are made on a weight/weight basis. Indications of relative amounts of a component characterized by a generic term are intended to refer to the total amount of all specific variants or members covered by said generic term. If a certain component defined by a generic term is specified to be present in a certain relative amount, and if this component is further characterized to be a specific variant or member covered by the generic term, it is intended that no other variants or members covered by the generic term are additionally present such that the total relative amount of components covered by the generic term exceeds the specified relative amount, more preferably, in such case, no other variants or members covered by the generic term are present at all.

[0027] The term "C2 to C4 alkanol" as used herein should be understood to encompass one or more C2 to C4 alkanes substituted with a hydroxy group (-OH). In one embodiment, an alkanol comprised in a formulation to be administered by an applicator of the invention is one or more selected from the group consisting of ethanol, isopropanol and n-propanol. In another embodiment said alkanol is ethanol. In a further embodiment, said alkanol is ethanol present in an amount of about 44.0%wt.

[0028] The term "polyalcohol" as used herein should be understood to encompass one or more of a C2 to C6 alkane or C2 to C6 alkene, substituted with two or more hydroxy groups.

[0029] In some embodiments, a polyalcohol comprised in a formulation to be administered by an applicator of the invention is one or more selected from the group consisting of ethylene glycol, propylene glycol, butylene glycol, and hexylene glycol. In one embodiment the polyalcohol is propylene glycol. In another embodiment the polyalcohol is propylene glycol present in an amount of about 20.0%wt.

[0030] The term "monoalkyl ether of diethylene glycol" as used herein should be understood to encompass one or more diethylene glycols substituted with a C1 to C6 alkyl ether.

[0031] In one embodiment, monoalkyl ether of diethylene glycol comprised in a formulation to be administered by an applicator ofthe invention is one or both of diethylene glycol monoethyl ether (DGME) and diethylene glycol monomethyl ether. In another embodiment, the monoalkyl ether of diethylene glycol is diethylene glycol monoethyl ether. In yet another embodiment, said monoalkyl ether of diethylene glycol is diethylene glycol monoethyl ether in an amount of about 5.0%wt.

[0032] The term "gelling agent" as used herein should be understood to encompass any agent capable of altering the viscosity of a formulation. A gelling agent used in a formulation to be administered by an applicator of the invention can be one or more selected from the group including: carbomer, carboxyethylene or polyacrylic acid such as carbomer or carbopol 980NF (CARBOPOLTM 980 NF) or 940 NF, 981 or 941 NF, 1382 or 1342 NF, 5984 or 934 NF, ETD 2020, 2050, 934P NF, 971P NF, 974P NF, and Noveon AA-1 USP, cellulose derivatives such as ethylcellulose (EC), hydroxypropylmethylcellulose (HPMC), ethylhydroxyethylcellulose (EHEC), carboxymethylcellulose (CMC), hydroxypropylcellulose (HPC) (Klucel different grades), hydroxyethylcellulose (HEC) (Natrosol grades), HPMCP 55, and Methocel grades, natural gums such as arabic, xanthan, guar gums, and alginates, polyvinylpyrrolidone derivatives such as Kollidon grades, polyoxyethylene-polyoxypropylene copolymers such as Lutrol F grades 68 and 127, chitosan, polyvinyl alcohols, pectins, and veegum grades. A tertiary amine, such as triethanolamine or trolamine, can also be included in the formulation to thicken and neutralize the system.

[0033] In one embodiment, the gelling agent comprised in a formulation to be administered by an applicator of the invention is a carbomer. Carbomer relates to a class of homopolymers of acrylic acid with a high molecular weight, which are cross-linked with any of several polyalcohol allyl ethers. Non-limiting examples of carbomers are carbomer 940, carbomer 973, carbomer 980NF, carbomer C980NF (wherein the digit indicates the average molecular weight of the polymer chains). In a particular embodiment, the gelling agent comprised in a formulation to be administered by an applicator of the invention is carbomer C980NF. In yet another embodiment, the gelling agent is carbomer C980NF in an amount of 1,20%wt.

[0034] The term "neutralizing agent" as used herein should be understood to encompass one or more agents capable of neutralizing an acidic or basic component of a formulation to be administered by an applicator of the invention in order to achieve a stable and homogeneous formulation. Non-limiting examples of a neutralizing agent include: diethylamine, diisopropylamine, a ternary amine such as triethanolamine or tromethamine, tetrahydroxypropylethylendiamine, and alkalis such as KOH or NaOH solution.

[0035] In one embodiment, a neutralizing agent comprised in a formulation to be administered by an applicator ofthe invention is triethanolamine (also named trolamine interchangeably). In another embodiment, the neutralizing agent is triethanolamine in an amount of about 0.35%wt.

[0036] The term "chelating agent" as used herein should be understood to encompass one or more agents which complex and segregate residual traces of free multivalent cations susceptible to cause the physical degradation of a gel matrix (thereby causing loss of viscosity and breakdown ofthe formulation).

[0037] In one embodiment, a chelating agent comprised in a formulation to be administered by an applicator of the invention is edetate disodium. In a further embodiment, the chelating agent is edetate disodium in an amount of about 0.06%wt.

[0038] As used herein the term "solvent" may encompass any type of solvent suitable for use in transdermal formulations and may be the same or different from any other component of a formulation to be administered by an applicator of the invention, as detailed herein above. In one embodiment, a solvent comprised in a formulation to be administered by an applicator of the invention is water.

[0039] In one embodiment, a formulation to be administered by an applicator of the invention comprises 2%wt of testosterone, C2 to C4 alkanol, polyalcohol, and monoalkyl ether of diethylene glycol, wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0040] The omission of long chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters provides formulations that do not have an unpleasant odor, irritation, and/or greasy texture caused by formulations that do include one or more of such compounds, resulting in greater patient compliance.

[0041] "Long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters" as used herein should be understood to encompass fatty alcohols and fatty acids having a branched or linear carbon body having 8 or more carbon atoms, and esters thereof, i.e. fatty esters having a branched or linear acid moiety having 8 or more carbon atoms or having a branched or linear alcohol moiety having 8 or more carbon atoms.

[0042] "Substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters" as used herein should be understood to mean comprising fatty alcohols, fatty acids and/or fatty esters in a total amount of less than about 0.1 %wt.

[0043] In one embodiment, a formulation to be administered by an applicator of the invention comprises 2%wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, and 5.0%wt of diethylene glycol monoethyl ether, wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0044] In a further embodiment, a formulation to be administered by an applicator of the invention comprises 2% wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, 5.0%wt of diethylene glycol monoethyl ether, 1.20%wt carbomer, 0.35%wt triethanolamine, 0.06%wt edetate disodium and water (q.s.) wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0045] In a further embodiment, a formulation to be administered by an applicator of the invention consists of 2% wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, 5.0%wt of diethylene glycol monoethyl ether, 1.20%wt carbomer, 0.35%wt triethanolamine, 0.06%wt edetate disodium and water (q.s.).

[0046] In yet a further embodiment, a formulation to be administered by an applicator of the invention comprises 1 % wt of testosterone, C2 to C4 alkanol, polyalcohol, and monoalkyl ether of diethylene glycol, wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0047] In another embodiment, a formulation to be administered by an applicator of the invention comprises 1% wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, and 5.0%wt of diethylene glycol monoethyl ether, wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0048] In a further embodiment, a formulation to be administered by an applicator of the invention comprises 1% wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, 5.0%wt of diethylene glycol monoethyl ether, 1.20%wt carbomer, 0.35%wt triethanolamine, 0.06%wt edetate disodium and water (q.s.) wherein said formulation is substantially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty esters.

[0049] In a further embodiment, a formulation to be administered by an applicator of the invention consists of 1% wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, 5.0%wt of diethylene glycol monoethyl ether, 1.20%wt carbomer, 0.35%wt triethanolamine, 0.06%wt edetate disodium and water (q.s.).

[0050] In some embodiments, a formulation to be administered by an applicator system of the invention further comprises at least one of a buffering agent, moisturizing agent, humectant, surfactant, antioxidant, emollient, or buffer.

[0051] In a specific embodiment, the invention provides an applicator system to transdermally administer testosterone or a derivative thereof to a patient in need thereof, e.g. for use in the treatment of a disease or disorder associated with reduced endogenous testosterone production.

[0052] "Diseases and disorders associated with reduced endogenous testosterone production" should be understood to encompass any disease or disorder which is directly or indirectly related to a condition of a mammalian subject wherein the endogenous production of testosterone is either reduced or substantially non-existent or terminated. Diseases and disorders associated with reduced endogenous testosterone production relate to hormonal disorders such as, but not limited to, for example hypogonadism, female sexual disorder, hypoactive sexual disorder, and adrenal insufficiency.

[0053] A viscous liquid, in particular a transdermal pharmaceutical formulation, can be topically applied by an applicator system of the invention to any body part, such as, but not limited to, the chest, thigh, inner thigh, abdomen, shoulder, upper arm, upper torso, back, neck, feet, hands, axilla, or scrotum. In one embodiment, a formulation in the form of a gel is applied to an area of skin of from about 100 cm2 up to about 1500 cm2.

[0054] In a further aspect the invention provides a kit comprising at least one applicator system of the invention comprising a formulation comprising testosterone as detailed above, and instructions for use thereof. In an embodiment, the instructions include at least the steps that the applicator is to be removed from the dispenser, a dose of gel be metered onto the application surface, and the dose be applied onto the skin.

[0055] In one embodiment, a kit of the invention comprises an applicator system which is adapted for dispensing a predetermined measured amount of said testosterone formulation. In a specific embodiment, the predetermined amount is 1.25 ml per dispense.

[0056] In yet another specific embodiment, the applicator system of the invention dispenses 1.25 ml per dispense of a formulation consisting of 2%wt of testosterone, 44.0%wt of ethanol, 20.0%wt of propylene glycol, 5.0%wt of diethylene glycol monoethyl ether, 1.20%wt carbomer, 0.35%wt triethanolamine, 0.06%wt edetate disodium and water (q.s.).

[0057] To provide more insight in the background ofthe present invention, attention is drawn to the following patent publications.

[0058] US 2005/0054991 relates to a dosing device for topically administering a pharmaceutical formulation directly to the skin of a mammal. The device comprises a housing capable of storing at least one unit dose of a pharmaceutical formulation; an applicator adapted for topically administering a unit dose of the pharmaceutical formulation directly onto the skin; and an actuator capable of metering a single unit dose of the pharmaceutical formulation from a first position in which the unit dose is stored in the housing to a second position in which the single unit dose is external to the device on the applicator so that the single unit dose can be topically administered.

[0059] US 2007/0000946 relates to a dispenser for metered dosing of cream-based medicines comprising a barrel, a base having a threaded rod extending therefrom, a riser having at least one flexible seal which engages the barrel, and an applicator cap having apertures therein for spreading dispensed cream onto a user's skin.

[0060] EP 1 514 492 relates to a device for storing and dispensing a cosmetic product, comprising a unit refillable with a product delivered from a container. The refillable unit has an application unit, e.g. a sponge.

[0061] US 2007/0166361 relates to formulations for transdermal or transmucosal administration of an active agent such as estradiol.

[0062] WO 2009/064762 discloses a dispenser including a body defining a supply chamber therein for retaining a supply of a composition. The dispenser further includes an application portion having a front side with a concave application surface disposed externally and being sufficiently large to receive the skin of a patient for application of the composition thereto, and a conduit fluidly communicating the supply chamber with the application surface for delivering the composition to the application surface from the supply chamber.

[0063] WO 2006/005135 discloses a container including a receptacle (numeral 6 in the Figures of WO 2006/005135) for holding a substance, drug or liquid, and having an opening (7) to the receptacle (6) through which the substance can be dispensed and having a circular and domed spreading surface (15) adjacent the opening for spreading and the accurate delivery of a thin layer of liquid over an area of skin. In the embodiment shown in Figure 15, the spreading surface (15) is of slightly convex form with radiused edges and circular shape. The receptacle (6) preferably holds between 50μΙ to 500μΙ of liquid having a viscosity of approximately 2.5 centipoises at an ambient temp of 20°.

[0064] WO 2007/140542 discloses an applicator (numeral 2 in the Figures of WO 2007/140542) for dispensing lotion from a dispensing device (1). The applicator includes a receptacle (13) for receiving a measured volume of lotion dispensed from the dispensing device (1). The receptacle (13) includes a collapsible reservoir space (15). Collapsing of the reservoir space (15) causes the lotion to pass through a passageway formed by apertures (18) in an outer member (14). An outer surface (21) of the outer member (14) provides a, preferably substantially convex, spreading surface for spreading the lotion on the treatment surface (20) of a user.

[0065] US 2010/217176 relates to a dermal flowable-composition dispenser that includes a body for retaining a supply of the composition, an application portion having an application surface, and a conduit connecting the supply chamber with the application surface for facilitating the reproducible delivery of a predetermined dose of the composition to the application surface. The application surface includes a concave application surface and a front side having an upper rim enclosing the application surface and forming a depression that has a volume that is greater than or equal to the volume of the predetermine dose.

[0066] US 6,648,538 relates to a device for dispensing a product, which device comprises a first reservoir containing the product to be dispensed, and a second reservoir in flow communication with the first reservoir via at least one passage having a cross-section that is smaller than a cross-section of the first reservoir. The device further comprises an application element configured to be accommodated in the second reservoir. An actuation mechanism is on a portion of the device other than the closure element, and is configured to move with respect to the first reservoir.

[0067] Within the framework ofthe present invention, the term "viscous liquid" includes, but is not limited to, gels, emulsions, creams, lotions and pastes.

[0068] The invention will now be explained in more detail with reference to the drawings, which schematically show a preferred embodiment according to the present invention.

Figure 1 is a perspective view of an applicator and dispenser according to the present invention.

Figure 2 is an exploded view of the applicator shown in Figure 1.

Figures 3A to 3D illustrate steps of a method of applying a viscous liquid to the human skin.

[0069] Figures 1 and 2 show an applicator system 1 for applying a transdermal pharmaceutical formulation to the human skin, in accordance with the present invention. The system comprises a metering dispenser 2 and an applicator 3 clamped onto the dispenser.

[0070] The dispenser 2 is a so-called airless metering dispenser comprising a cylindrical housing 4 and a metering pump 5. The housing contains a pouch (not shown), e.g. made of an aluminium and polyethylene multilayer foil, to ensure protection of the liquid inside against oxygen and UV rays. The metering pump is actuated by pushing and delivers a constant and precise dose of, e.g. 1.25 ml +/- 5% with each actuation. Suitable airless metering pumps are commercially available, e.g. from Lablabo.

[0071] The applicator comprises a convex, continuous application surface 6 for receiving a metered amount of the viscous liquid from the dispenser 2. In this example, the surface is part of an insert 7 which is clamp fitted and/or welded into the distal end of a sleeve 8. The insert is made of a plastomer, e.g. acrylonitrile butadiene styrene (ABS), having a Young's modulus of e.g. 3 GPa. The application surface is smooth, with a texture of stage 21 (measured in accordance with VDI 3400 standard) or smoother.

[0072] The surface 6 is provided with a symbol 9 to indicate the optimum location for metering the viscous liquid onto it. In this example, the symbol comprises a drop and a circle surrounding the drop to indicate the boundary ofthe optimum location.

[0073] As shown in Figure 1, the applicator doubles as a cap for the dispenser. To this end, the sleeve 8, with its proximal end, fits clampingly about the dispenser 2.

[0074] In this example, the applicator has a length of 118 millimeters and approximately 90% of the length of the sleeve is provided with an elastomeric grip 10. The grip ends at some distance from the application surface to provide a barrier between the two.

[0075] To prevent any residues from rubbing off on other surfaces, e.g. towels or persons, such as family members of the user of the applicator system, a hygiene cap 11, made of e.g. polycarbonate, is provided to cover the application surface after use.

[0076] Figures 3Ato 3D illustrate the typical steps of a method of applying a gel to the human skin with the present applicator. The hygiene cap is removed from the application surface (Figure 3A) and the applicator is removed from the dispenser (Figure 3B), in no specific order. A single dose of gel is metered onto the application surface (Figure 3C) and the dose is applied onto the skin, preferably spreading the gel over a wider area (Figure 3D) to facilitate uptake. If a double or triple amount is indicated, these latter two steps can be repeated accordingly.

[0077] The applicator system according to the present invention allows use of standard metering pumps, made in large quantities and thus providing good accuracy at relatively low costs, and enables substantially complete transfer ofthe amount of viscous liquid metered onto the application surface from that surface to the skin.

Experiments [0078] A phase 2, open-label, sequential dose escalation study in 18 adult hypogonadal males, i.e. males having a baseline morning serum testosterone concentration <300 ng/dL, was carried out to evaluate the pharmacokinetics of three volumes (1.25, 2.50 and 3.75 mL) of a testosterone gel formulation. The gel formulation consisted of 2%wt of testosterone, 44%wt of ethanol, 20.0%wt of propylene glycol, 5%wt of monoethyl ether of diethylene glycol, 1,20%wt of carbomer, 0.35%wt of triethanolamine, 0.06%wt of edetate disodium and water (hereinafter "the gel"). It was administered to the shoulder/upper arm either with the applicator shown in the Figures and described above or by hand application.

[0079] Objectives ofthe study in adult hypogonadal males were to: 1. 1. investigate the steady-state pharmacokinetics of total testosterone (and dihydrotestosterone (DHT)) after 7 days of treatment with each of three volumes (1.25, 2.50 and 3.75 mL) of the gel applied with an applicator of the invention to the shoulder/upper arm; 2. 2. investigate the steady-state pharmacokinetics of total testosterone (and DHT) after 7 days of treatment with one volume (2.50 mL) of the gel applied by hand to the shoulder/upper arm.

[0080] The gel, when administered by an applicator of the invention, was delivered in aliquots of 1.25 mL (23 mg/pump actuation). A total of 1.25 mL (23 mg, 1 pump actuation), 2.50 mL (46 mg, 2 pump actuations) or 3.75 mL (70 mg, 3 pump actuations) were administered per application.

[0081] Subjects applied 2.50 mL of the gel by hand for 7 days, followed by a 7-day washout period. After the washout, subjects applied three volumes of the gel (1.25, 2.50 and 3.75 mL) in a sequentially escalating fashion with an applicator ofthe invention, with no washout period between treatment phases (each seven days). Total testosterone and DHT blood levels were determined pre-application and at 2, 4, 6, 8, 10, 12 and 24 hours post-application on Visits 4 (2.50 mL, hand), 7 (1.25 mL, applicator), 9 (2.50 mL, applicator) and 11 (3.75 mL, applicator) for the determination of AUCt (Area Under the Curve), Cmax (maximum concentration), Cavg (average concentration), and Estimated Responder Rate (percentage of patients having a concentration of total testosterone in the therapeutic range, 300 to 1050 ng/dL). The patient was also asked to state his preference for a particular method of application.

[0082] The duration of the treatment period for each subject from the screening visit to the last visit was approximately 70 days. Ό083] The results are shown in Tables 1 and 2 below.

[0084] Table 1 shows a substantially proportional increase of AUCt, Cmax, and Cavg with increased dosage, confirming that the applicator provides accurate transfer of the metered amounts of the gel from the application surface to the skin. This proportionality can be employed to relatively quickly establish the correct dosage for a particular patient.

[0085] Table 2 shows a reduced variability of AUCt, Cmax, and Cavg, when the gel is applied with the applicator instead of by hand. This too confirms more accurate transfer. Further, Table 2 shows a higher responder rate indicating an increased efficacy of the gel when it is applied with the applicator according to the present invention.

[0086] Also, 15 of the 18 subjects preferred use of the applicator over application by hand, i.e. the applicator provides an incentive for correct and efficacious administration ofthe gel.

[0087] The invention is not restricted to the above-described embodiments which can be varied in a number of ways within the scope of the claims.

REFERENCES CITED IN THE DESCRIPTION

This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all

liability in this regard.

Patent documents cited in the description • US7198801B [00211 • EP2012050695W [00221 • US20050054991A [00581 • US20070000946A [00591 • EP1514492A røøSOl • US20070166361A [0061] • W02009064762A [0062] • W02006005135A [00631 [00631 • W02007140542A [00641 [00641 • US2010217176A [0065] • US6648538B [00661

Non-patent literature cited in the description • CHEMICAL ABSTRACTS, 58-22-0 [0018]

Claims (21)

An application system (1) for applying a viscous liquid, especially a transdermal pharmaceutical formulation, to the human skin, comprising: a measuring dispenser (2) comprising a container holding the viscous liquid and a pump (5). ) for measuring the liquid and an application unit (3) removably connected to the dispenser (2), comprising an application surface (6) for receiving a measured amount of the liquid from the dispenser (2), characterized in that the application surface (6) is convex and continuous, and in that a hygiene cap (11) is provided to cover the application surface (6). The application system (1) of claim 1, wherein the application surface (6) is rigid. The application system (6) of claim 2, wherein the material of which the application surface (6) is made has a Young's modulus of at least 1.5 GPa. The application system (1) of claim 2 or 3, wherein the application surface (1) has a texture similar to step 21 or smoother. The application system (1) according to any one of the preceding claims, wherein the dispenser (2) has a measurement accuracy of +/- 15% and / or is configured to provide a measured amount per meter. administration in a range of 0.5 to 2.5 ml. The application system (1) according to any one of the preceding claims, wherein the application unit (3) acts as a cap for the dispenser (2). Application system (1) according to claim 6, wherein the application unit (3) comprises a sleeve (8) for receiving and securing the dispenser (2). The application system (1) of claim 7, wherein the application unit (3) has a total length of at least 6.5 centimeters and / or at least 50% of the length of the application unit (3) is suitable as a handle (10). The application system (1) according to any one of the preceding claims, wherein the application surface (6) comprises a symbol (9) to mark the optimum location for measuring the viscous liquid. Application system (1) according to any one of the preceding claims, wherein the viscous liquid has a viscosity of at least 3000 centipoise at 25 ° C. An application system (1) according to any one of the preceding claims, wherein the viscous liquid contains testosterone or a derivative thereof. An application system (1) according to any one of the preceding claims, wherein the pharmaceutical formulation comprises at least one active agent and a solvent system present in an amount sufficient to dissolve the at least one active agent. The application system (1) of claim 12, wherein the at least one active agent is testosterone or a derivative thereof. The application system (1) according to claim 12 or 13, wherein the formulation comprises alkanol in an amount of between about. 5-50% by weight of polyalcohol in an amount of between approx. 1 to 30% by weight, permeation amplifier in an amount of between approx. 0.2-25%, gelling agent in an amount of between approx. 0.05-4% by weight, neutralizing agent in an amount of between approx. 0.05-1% by weight and chelating agent in an amount of between approx. 0.001-5.0% by weight. The application system (1) of claim 14, wherein the formulation comprises 1 wt.% - 2 wt.% Testosterone, C fatty esters. The application system (1) of claim 15, wherein the formulation comprises 1 wt% - 2 wt% testosterone, 44.0 wt% ethanol, 20.0 wt% propylene glycol and 5.0 wt% diethylene glycol monoethyl ether wherein the formulation essentially free of long-chain fatty alcohols, long-chain fatty acids, and long-chain fatty acid esters. The application system (1) of claim 16, wherein the formulation comprises 1% by weight - 2% by weight of testosterone, 44.0% by weight ethanol, 20.0% by weight propylene glycol, 5.0% by weight diethylene glycol monoethyl ether, 1.20% by weight -% carbomer, 0.35% wt% triethanolamine, 0.06 wt% disodium edetate and water, wherein the formulation is essentially free of long chain fatty alcohols, long chain fatty acids and long chain fatty acid esters. The application system (1) of claim 17, wherein the formulation is comprised of 1 wt% - 2 wt% testosterone, 44.0 wt% ethanol, 20.0 wt% propylene glycol, 5.0 wt% diethylene glycol monoethyl ether, 1 , 20 wt% carbomer, 0.35 wt% triethanolamine, 0.06 wt% disodium edetate and water. The application system (1) of claims 15-18, wherein the formulation comprises 2% by weight of testosterone. A kit comprising an application system (1) according to any one of the preceding claims as well as instructions for use thereof. The kit according to claim 20, which is intended for dispensing 1.25 ml per ml. administration of a formulation consisting of 2 wt% testosterone, 44.0 wt% ethanol, 20.0 wt% propylene glycol, 5.0 wt% diethylene glycol monoethyl ether, 1.20 wt% carbomer, 0.35% wt% triethanolamine, 0.06 wt% disodium edetate and water.