Pfizer, a United States-based pharmaceutical company, has received an exclusive option to acquire gene therapy firm, Vivet Therapeutics.
It was reported yesterday that the deal is valued at around EUR560m.
Pfizer has paid around EUR45m to purchase a 15% equity interest in Vivet Therapeutics, and will pay up to EUR560m that includes an option exercise payment and certain clinical, regulatory, and commercial milestone payments.
Both firms will work on the development of VTX-801, which is Vivet's novel investigational gene therapy for Wilson disease, a rare, chronic, and potentially life-threatening liver disorder of impaired copper transport, which causes serious copper poisoning. The product has received orphan drug designation from the US Food and Drug Administration (FDA) and the European Commission (EC). Pfizer has an option to acquire 100% interest in Vivet, following its delivery of certain data from the Phase I/II clinical trial for VTX-801.
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