Drug intelligence / Profile preview

LUT-017

Development stage
Phase 1
Lead developer
Lutris Pharma
Modality
Small Molecules
Administration
Topical
01

Overview

LUT-017 is a novel small molecule B-Raf inhibitor developed by Lutris Pharma. It is designed for topical application to the skin and leverages the paradoxical effect of B-Raf inhibition in non-mutated cells to stimulate skin stem cell proliferation and accelerate wound healing. Unlike its use in oncology (where B-Raf inhibition leads to tumor shrinkage), topical application of LUT-017 in normal skin promotes regeneration and keratinocyte proliferation. The primary indication under investigation is for non-healing wounds such as venous leg ulcers, particularly targeting populations with diabetes, obesity, or limited mobility. As of now, development remains at the preclinical stage[1][4].

Other names
1,5-Isoquinolinediamine N1-[4-chloro-3]
02

Targets

BRAF (B-Raf proto-oncogene, serine/threonine kinase)EPHA5ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)LYN (LYN proto-oncogene, Src family tyrosine kinase)EPHB4 (Ephrin type-B receptor 4)MAPK14 (p38 mitogen-activated protein kinase alpha)RAF1 (c-Raf-1 (Y340D/Y341D))

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