Drug intelligence / Profile preview

repifermin

Development stage
Phase 2
Lead developer
GSK
Modality
Recombinant Proteins and Enzymes
Administration
Intravenous, Topical, Rectal
01

Overview

Repifermin is a recombinant human keratinocyte growth factor 2 (KGF-2), also known as fibroblast growth factor 10 (FGF-10). It is a member of the fibroblast growth factor family and acts as an agonist at the Fibroblast growth factor receptor 1 (FGFR1) and Fibroblast growth factor receptor 2 (FGFR2). Repifermin was developed to promote epithelial cell proliferation, enhance wound healing, and reduce inflammation in various conditions such as chronic venous ulcers, mucositis, neutropenia, and ulcerative colitis. Preclinical studies demonstrated its ability to accelerate wound healing and improve mucosal transport in animal models of colitis. Clinical trials showed that it was well tolerated but did not demonstrate significant efficacy for ulcerative colitis or other indications at tested doses. Development has been discontinued for all investigated indications[1][4][7].

Brand names
repifermin
Other names
repiferminkeratinocyte growth factor 2fibroblast growth factor 10
02

Targets

FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)

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