IP Library Granted Patent US 11,185,487
Granted Patent B2
US 11,185,487 · App. 15/387,634 · Granted Nov 30, 2021

Hair growth composition and method

Inventor: Jeffrey M. Wu (Princeton, NJ)
Assignee: Johnson & Johnson Consumer Inc.
A61K8/4953A61K8/14A61K8/34A61K8/345A61K8/347A61K8/362A61K8/365A61K8/37A61K8/39A61K8/731A61K8/86A61K9/0014A61K31/506A61K47/14A61K47/38A61Q7/00A61K2800/262A61K2800/48A61K2800/49A61K2800/52A61K2800/594
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Quick Facts
Patent No.
US 11,185,487
App. No.
15/387,634
Granted
Nov 30, 2021
Kind
B2
Abstract

The present invention relates to compositions for and methods of retarding hair loss or facilitating hair growth comprising a hair growth active, a C 8 -C 24 alcohol ester of a carboxylic acid and a viscosity modifying agent comprising: a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1.

Claims (98)

1. A composition comprising:

a. liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm comprising:

i. one or more of a hair growth or hair regrowth compound represented by formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), each R 3 and R 4 individually is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof; and

ii. from about 2% to about 7.5% by weight of an oil phase comprising an C 8 -C 24 alcohol ester of a carboxylic acid and steareth-10;

b. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1; and

c. a pharmaceutically acceptable topical carrier comprising, one or more solubilizer(s), one or more solubilizing acid(s) or mixtures thereof

wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition and wherein the liquid vesicles are suspended within the pharmaceutically acceptable topical carrier.

2. The composition of claim 1 , wherein the solubilizer comprises one or more C 1 -C 3 alcohol(s), one or more polyhydric alcohol(s) or mixtures thereof.

3. The composition of claim 1 , wherein the one or more of a hair growth or hair regrowth compound represented by formulas I or II is minoxidil and further wherein the composition comprises from about 0.1% to about 15% of the minoxidil or a pharmaceutically acceptable salt thereof by weight.

4. The composition of claim 3 , wherein the composition comprises from about 0.5% to about 10% of the minoxidil or a pharmaceutically acceptable salt thereof by weight.

5. The composition of claim 1 , wherein the pharmaceutically acceptable carrier also comprises minoxidil or a pharmaceutically acceptable salt thereof.

6. The composition of claim 1 , wherein said C 8 -C 24 alcohol ester of a carboxylic acid is an ester of cetyl alcohol.

7. The composition of claim 1 , wherein said C 8 -C 24 alcohol ester of a carboxylic acid is a lactic acid ester.

8. The composition of claim 7 , wherein said C 8 -C 24 alcohol ester of a carboxylic acid is cetyl lactate.

9. The composition of claim 7 , wherein said C 8 -C 24 alcohol ester of a carboxylic acid is myristyl lactate.

10. The composition of claim 7 , wherein said C 8 -C 24 alcohol ester of a carboxylic acid is a mixture of C 12 -C 15 alkyl lactates.

11. The composition of claim 1 , wherein the composition comprises from about 0.1% to about 15%, by weight, of the polyoxyethylene C 4 -C 26 fatty ether.

12. The composition of claim 1 wherein the ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose is greater than about 3:1.

13. The composition of claim 1 wherein the ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose is no greater than about 10:1.

14. The composition of claim 12 wherein the composition has a viscosity of from about 50 cps to about 30000 cps as measure by Brookfield RV at spindle 4, speed 6 RPM.

15. The composition of claim 14 wherein the composition has a viscosity of from about 100 cps to about 10000 cps as measure by Brookfield RV at spindle 4, speed 6 RPM.

16. The composition of claim 1 wherein the composition comprises from about 0.1% to about 40% by weight of the one of more C 1 -C 3 alcohols.

17. The composition of claim 16 wherein the one or more C 1 -C 3 alcohols comprises ethanol.

18. The composition of claim 1 wherein the liquid vesicle is a non-phospholipid liquid vesicle.

19. The composition of claim 1 wherein the liquid vesicles have an average diameter of from about 0.05 μm to about 20 μm.

20. The composition of claim 1 wherein the carboxymethyl degree of substitution of the carboxymethyl cellulose is from about 0.6 to about 0.9.

21. The composition of claim 20 wherein the carboxymethyl degree of substitution of the carboxymethyl cellulose is about 0.7.

22. The composition of claim 1 wherein the average degree of polymerization of the carboxymethyl cellulose is from about 2500 to about 3500.

23. The composition of claim 22 wherein the average degree of polymerization of the carboxymethyl cellulose is about 3200.

24. The composition of claim 1 wherein the weight average molecular weight of the carboxymethyl cellulose is from about 650,000 to about 750,000.

25. The composition of claim 24 wherein the weight average molecular weight of the carboxymethyl cellulose is from about 675,000 to about 730,000.

26. A composition comprising:

a. one or more of a hair growth or hair regrowth compound represented by the Formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), Each R 3 and R 4 individually is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof;

b. from about 2% to about 7.5% by weight of an oil phase oil phase comprising a C 8 -C 24 alcohol ester of a carboxylic acid and steareth-10; and

c. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1; and

d. a pharmaceutically acceptable topical carrier comprising one or more solubilizers, one or more solubilizing acids or mixtures thereof,

wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm and further wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition.

27. A composition comprising:

a. minoxidil or pharmacologically acceptable acid addition salts thereof;

b. from about 2% to about 7.5% by weight of an oil phase comprising cetyl lactate, myristyl lactate or mixtures thereof and steareth-10;

c. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1; and

d. a pharmaceutically acceptable topical carrier comprising:

i. ethanol;

ii. lactic acid;

iii. pentylene glycol; and

iv. glycerin,

wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm and further wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition.

28. A composition comprising liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm suspended within a pharmaceutically acceptable liquid carrier, wherein the liquid vesicles comprise:

a. minoxidil or pharmacologically acceptable acid addition salts thereof; and

b. from about 2% to about 7.5% by weight of an oil phase comprising a C 8 -C 24 alcohol ester of a carboxylic acid, optionally, wherein said C 8 -C 24 alcohol ester of a carboxylic acid is an ester of cetyl alcohol, optionally, wherein said C 8 -C 24 alcohol ester of a carboxylic acid is a lactic acid ester, or optionally wherein said C 8 -C 24 alcohol ester of a carboxylic acid is an ester of myristyl alcohol and steareth-10; and

wherein the pharmaceutically acceptable liquid carrier comprises:

i. one or more solubilizers, one or more solubilizing acids or mixture thereof; and

ii. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1 wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition.

29. A composition comprising:

a. minoxidil or pharmacologically acceptable acid addition salts thereof;

b. from about 2% to about 7.5% by weight of an oil phase comprising a C8-C24 alcohol ester of a carboxylic acid and steareth-10;

c. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1; and

d. a pharmaceutically acceptable liquid carrier comprising one or more solubilizers, one or more solubilizing acids or a mixture thereof, wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm and further wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition.

30. A composition comprising:

a. minoxidil or pharmacologically acceptable acid addition salts thereof;

b. from about 2% to about 7.5% by weight of an oil phase oil phase comprising cetyl lactate, myristyl lactate or mixtures thereof and steareth-10;

c. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1; and

d. a pharmaceutically acceptable topical carrier comprising:

i. ethanol;

ii. lactic acid;

iii. pentylene glycol or propylene glycol; and

iv. glycerin,

wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm and further wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition.

31. A method for growing hair in a subject in need of such treatment comprising topically applying the composition of claim 1 to the subject on an area where hair growth is desired.

32. A method for improving storage stability of a composition for retarding hair loss or facilitating hair growth or regrowth, comprising the step of adding to the composition a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1 to 10:1 wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition, the composition comprising:

a. one or more liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm, the vesicles comprising:

i. a hair growth compound represented by formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), each R 3 and R 4 individually being selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof;

ii. a C 8 -C 24 alcohol ester of a carboxylic acid; and

b. a pharmaceutically acceptable topical carrier comprising one or more solubilizers, one or more solubilizing acids or mixtures thereof,

wherein the composition is storage stable at 40° C. and at 5° C. for at least 1 week.

33. A method for improving storage stability of a composition for retarding hair loss or facilitating hair growth or regrowth, comprising the step of adding to the composition a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1 to 10:1 wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition, the composition comprising:

a. from about 0.1% to about 20% of one or more pharmaceutically acceptable addition salts of a compound represented by formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), each R 3 and R 4 individually being selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof;

b. from about 0.5% to about 10% by weight of an oil phase; and

c. from about 0 to about 25% of a C 2 -C 4 alcohol

wherein the composition has a pH of about 3 to about 5, wherein the composition is storage stable at 40° C. and at 5° C. for at least 1 week, and wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm.

34. A hair growth or hair regrowth composition comprising:

a. from about 0.1% to about 20% of one or more pharmaceutically acceptable addition salts of a compound represented by formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), each R 3 and R 4 individually being selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof;

b. from about 2% to about 7.5% by weight of an oil phase comprising myristyl lactate and steareth-10

c. from about 0 to about 25% of a C 2 -C 4 alcohol; and

d. a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1 to 10:1 wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition

wherein the composition has a pH of about 3 to about 5, wherein the composition is storage stable at 40° C. and at 5° C. for at least 1 week, and wherein the composition comprises liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm.

35. A method for improving storage stability of a composition for retarding hair loss or facilitating hair growth or regrowth, comprising the step of adding to the composition a viscosity modifying agent comprising a nonionic hydroxypropylmethyl cellulose and a high molecular weight carboxymethyl cellulose at a ratio of the nonionic hydroxypropylmethyl cellulose to the high molecular weight carboxymethyl cellulose of greater than about 1:1 to 10:1 wherein the total concentration of the nonionic hydroxypropylmethyl cellulose and the high molecular weight carboxymethyl cellulose is from about 0.5% to about 3% by weight of the total composition, the composition comprising:

a. one or more liquid non-phospholipid multilayer vesicles having an average diameter of from about 0.05 μm to about 20 μm, the vesicles comprising:

i. a hair growth compound represented by formulas I or II:

and mixtures thereof, wherein R 1 is hydrogen or —N(R 3 )(R 4 ), each R 3 and R 4 individually being selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower aralkyl, and lower cycloalkyl, and taken together R 3 and R 4 may be a heterocyclic moiety selected from the group consisting of aziridinyl, azetidinyl, pyrrolidinyl, piperidino, hexahydroazepinyl, heptamethylenimino, octamethylenimino, morpholino, and 4-lower-alkylpiperazinyl, each of said heterocyclic moieties having attached as substituents on the carbon atoms 0 to 3 lower alkyl groups, hydroxy or alkoxy, and wherein R 2 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, lower alkoxyalkyl, lower cycloalkyl, lower aryl, lower aralkyl, lower alkaryl, lower alkaralkyl, lower alkoxyaralkyl, and lower haloaralkyl; tautomers thereof and pharmacologically acceptable acid addition salts thereof;

ii. a C8-C24 alcohol ester of a carboxylic acid; and

b. a pharmaceutically acceptable topical carrier comprising one or more solubilizers, one or more solubilizing acids or mixtures thereof,

wherein the composition is does not separate into two or more distinct phases after storage at 40° C. and at 5° C. for at least 1 week.

Assignments (7)
CHANGE OF NAME Recorded Oct 28, 2024
From: JOHNSON & JOHNSON CONSUMER INC.
To: KENVUE BRANDS LLC
Reel/Frame 069267/0143 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2023
From: JOHNSON & JOHNSON CONSUMER INC.
To: JOHNSON & JOHNSON CONSUMER INC.
Reel/Frame 062438/0372 →
CERTIFICATE OF CONVERSION Recorded Jan 19, 2023
From: JOHNSON & JOHNSON CONSUMER INC.
To: JOHNSON & JOHNSON CONSUMER INC.
Reel/Frame 062438/0521 →
MERGER Recorded Jan 27, 2022
From: JOHNSON & JOHNSON CONSUMER INC.
To: CHENANGO ZERO LLC
Reel/Frame 059618/0521 →
MERGER Recorded Jan 27, 2022
From: CHENANGO ZERO LLC
To: CHENANGO TWO LLC
Reel/Frame 058888/0133 →
MERGER AND CHANGE OF NAME Recorded Jan 27, 2022
From: CHENANGO TWO LLC; CURRAHEE HOLDING COMPANY INC.
To: JOHNSON & JOHNSON CONSUMER INC.
Reel/Frame 058888/0210 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2017
From: WU, JEFFREY M.
To: JOHNSON & JOHNSON CONSUMER INC.
Reel/Frame 041127/0814 →
Continuity (2)
Provisional Application 62271405 · Dec 28, 2015
Related Publication 20170181948A1 · Jun 29, 2017