GlaxoSmithKline (LON: GSK) will sell the rights to its experimental dermatology drug, tapinarof, to Roivant Sciences' subsidiary Dermavent Sciences, Pharmafile reported on Friday.
Dermavent paid an upfront payment of GBP150 for the rights to tapinarof. It has also agreed to pay GSK future milestone payments of an additional GBP100m upon the achievement of prespecified developmental targets.
Completion of the deal will give Dermavent the global rights to the drug in all countries except China.
The drug has been studied as a treatment for psoriasis and atopic dermatitis (eczema). It was found to have demonstrated clinically meaningful results in treating adults with plaque psoriasis in a Phase IIb study involving 227 patients.
A separate double-blind, placebo-controlled Phase IIb study involving 247 patients with atopic dermatitis also resulted in the drug demonstrating efficacy.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA