New long-acting injectable compositions comprising finasteride for the prevention or treatment of androgenetic alopecia

By developing a long-acting subcutaneous injection composition of finasteride, the problem of daily administration of oral finasteride preparations has been solved, achieving continuous inhibition of type II 5α-reductase for more than one month, thus improving the stability and efficacy of treating androgenetic alopecia.

CN122396481APending Publication Date: 2026-07-14INVENTAGE LAB INC

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
INVENTAGE LAB INC
Filing Date
2024-12-19
Publication Date
2026-07-14

AI Technical Summary

Technical Problem

Existing oral finasteride formulations require daily administration and cannot sustain the inhibition of type II 5α-reductase for more than one month, leading to recurring symptoms of androgenetic alopecia. Furthermore, the drug has a short half-life, resulting in unstable treatment efficacy.

Method used

Develop a long-acting subcutaneous injection composition containing finasteride, which can inhibit type II 5α-reductase for more than one month with a single injection, increase the in vivo half-life of finasteride to 100-160 hours, and be administered subcutaneously using a microparticle LAI formulation, comprising a uniformly mixed microsphere of biodegradable polymer and finasteride.

Benefits of technology

It achieves sustained release of finasteride in the body for more than one month, inhibits the conversion of testosterone to DHT, improves the stability and predictability of the treatment of androgenetic alopecia, and enhances the uniformity of treatment effects.

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Abstract

The present invention relates to a new long-acting injection composition for preventing or treating androgenetic alopecia, which contains finasteride, inhibits type Ⅱ 5α-reductase for more than 1 month by a single injection, limits the conversion of testosterone into DHT, and can reduce androgen-mediated miniaturization of hair follicles. In addition, after in vivo injection, the average half-life (t1 / 2el) of finasteride is increased, thereby enabling improved stability, and a more predictable and uniform therapeutic effect can be exhibited compared to oral preparations.
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