IP Library Granted Patent US 11,179,443
Granted Patent B2
US 11,179,443 · App. 15/559,865 · Granted Nov 23, 2021

Stabilized external preparation comprising thymosin beta 4 as an active ingredient

Inventors: Jun Won Choi (Seoul, KR); Kyoungsun Kim (Busan, KR); Si Young Lee (Ansan-si, KR); Tae Heum Um (Seoul, KR)
Assignee: G-TREEBNT CO., LTD.
A61K38/2292A61K9/0014A61K9/06A61K47/02A61K47/10A61K47/183A61K47/26A61K47/32A61K47/38
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Quick Facts
Patent No.
US 11,179,443
App. No.
15/559,865
Granted
Nov 23, 2021
Kind
B2
Abstract

The present invention relates to a stabilized external preparation comprising thymosin beta 4 (Tβ4) as an active ingredient. More specifically, the present invention relates to a therapeutically effective external preparation with improved stability and biological activity of Tβ4. The preparation according to the present invention provides Tβ4 in a stable state by maintaining the biological activity of Tβ4 and minimizing the generation of Tβ4 sulfoxide through oxidization reactions and multimers through aggregation.

Claims (22)

1. A method for treating skin damage of a subject, comprising administering an external preparation to a damaged site of a skin of the subject,

wherein the treatment of the skin damage includes wound closure and tissue regeneration;

wherein the external preparation comprises

thymosin beta 4 (Tβ4) as an active ingredient in an amount of 172 mg based on the total amount 548 g of the external preparation,

a phosphate buffer;

an additive that is propylene glycol in an amount of 5.75 g and/or disodium-EDTA dihydrate in an amount of 63 mg, both based on the total amount 548 g of the external preparation; and

a sodium carboxymethyl cellulose as a viscosifier, in an amount of 14.4 g based on the total amount 548 g of the external preparation; and

wherein the external preparation has a pH of 5.5-6.0.

2. The method of claim 1 , wherein the skin damage is pressure ulcer, foot ulcer, epidermolysis bullosa, oral mucositis, or hidradenitis suppurativa.

3. The method of claim 2 , wherein the skin damage comprises inflammation.

4. The method of claim 1 , wherein the viscosity (cP) of the external preparation is in a range of 3 to 100,000 at 25° C.

5. The method of claim 1 , wherein the external preparation is formulated into a form of a gel, a cream, a paste, an ointment, a liniment, a lotion, a hydrogel or an aerosol.

6. A method for treating skin damage of a subject, comprising administering an external preparation to a damaged site of a skin of the subject,

wherein the treatment of the skin damage includes wound closure and tissue regeneration;

wherein the external preparation comprises

thymosin beta 4 (Tβ4) as an active ingredient in an amount of 172 mg based on the total amount 548 g of the external preparation,

a phosphate buffer,

an additive that is propylene glycol in an amount of 5.75 g and/or disodium-EDTA dihydrate in an amount of 63 mg, both based on the total amount 548 g of the external preparation; and

a sodium carboxymethyl cellulose as a viscosifier, in an amount of 14.4 g based on the total amount 548 g of the external preparation,

sterile water,

sodium chloride, and

HCl to adjust a pH of the external preparation to 5.5-6.0.

Assignments (2)
CHANGE OF NAME Recorded Dec 3, 2021
From: G-TREEBNT CO., LTD.
To: HLB THERAPEUTICS CO., LTD.
Reel/Frame 058905/0456 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 20, 2017
From: CHOI, JUN WON; KIM, KYOUNGSUN; LEE, SI YOUNG; UM, TAE HEUM
To: G-TREEBNT CO., LTD.
Reel/Frame 043637/0544 →
Priority Claims (1)
KR 10-2017-0027706 · Mar 3, 2017 · national
Continuity (1)
Related Publication 20180280479A1 · Oct 4, 2018