US2020330446A1PendingUtilityA1

Compositions and methods of treating skin fibrotic disorders

Assignee: AIVIVA BIOPHARMA INCPriority: Oct 7, 2015Filed: Jul 2, 2020Published: Oct 22, 2020
Est. expiryOct 7, 2035(~9.2 yrs left)· nominal 20-yr term from priority
A61K 31/506A61K 31/496A61K 31/404A61P 17/02A61P 17/00A61K 31/47A61K 31/454A61K 31/5025A61K 31/4439A61K 31/44A61K 31/497
56
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Claims

Abstract

A method for preventing and/or modulating formation of a dermal fibrotic disorder includes administering a therapeutically effective amount of a multi-phase modulator to a subject in need thereof. The multi-phase modulator is selected from the group consisting of axitinib, nintedanib, sorafenib, sunitinib, lenvatinib, panatinib, pazopanib, regorafenib, and riociguat. The dermal fibrotic disorder is acne scars, skin scars such as keloids and hypertrophic scars, wrinkles, cellulite and dermal neoplastic fibrosis, scarring alopecia, various vasculopathy, vasculitis, burn wound healing, diabetic foot syndrome, scleroderma, arthrofibrosis, peyronie's disease, dupuytren's contracture, or adhesive capsulitis

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for modulating formation of a dermal fibrotic disorder, comprising:
 administering to a subject a therapeutically effective amount of multi-kinase inhibitor selected from the group consisting of nintedanib, lenvatinib, or a combination thereof;   wherein the dermal fibrotic disorder is aberrant wound-healing, wrinkle, cellulite and dermal neoplastic fibrosis, vasculopathy, vasculitis, exuberant burn wound-healing, diabetic foot syndrome, arthrofibrosis, or Peyronie's disease.   
     
     
         2 . The method according to  claim 1 , wherein the multi-kinase inhibitor is nintedanib. 
     
     
         3 . The method according to  claim 1 , wherein the multi-kinase inhibitor is lenvatinib. 
     
     
         4 . The method according to  claim 1 , wherein the subject is a human. 
     
     
         5 . The method according to  claim 1 , wherein the administering is by intramuscular injection, intradermal injection, intralesional injection, subcutaneous injection, topical application, localized administration or by injection into a joint. 
     
     
         6 . The method according to  claim 1 , wherein the dermal fibrotic disorder is aberrant wound-healing. 
     
     
         7 . The method according to  claim 2 , wherein the dermal fibrotic disorder is aberrant wound-healing. 
     
     
         8 . The method according to  claim 3 , wherein the dermal fibrotic disorder is aberrant wound-healing. 
     
     
         9 . The method according to  claim 1 , wherein the dermal fibrotic disorder is wrinkle. 
     
     
         10 . The method according to  claim 1 , wherein the dermal fibrotic disorder is cellulite and dermal neoplastic fibrosis. 
     
     
         11 . The method according to  claim 1 , wherein the dermal fibrotic disorder is vasculopathy. 
     
     
         12 . The method according to  claim 1 , wherein the dermal fibrotic disorder is vasculitis. 
     
     
         13 . The method according to  claim 1 , wherein the dermal fibrotic disorder is exuberant burn wound-healing. 
     
     
         14 . The method according to  claim 1 , wherein the dermal fibrotic disorder is diabetic foot syndrome. 
     
     
         15 . The method according to  claim 1 , wherein the dermal fibrotic disorder is arthrofibrosis. 
     
     
         16 . The method according to  claim 1 , wherein the dermal fibrotic disorder is Peyronie's disease.

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