Biotechnology company TME Pharma N.V. (Euronext Growth Paris:ALTME) said on Thursday that it has signed a binding exclusive negotiation agreement with Japanese clinical-stage biotechnology company TMS Co Ltd to negotiate a definitive agreement covering worldwide rights to its oncology candidate NOX-A12 (olaptesed pegol).
TMS will pay TME Pharma a non-refundable EUR150,000 fee for a six-month exclusivity period, which may be extended through additional payments.
Under non-binding proposed terms, TME Pharma would receive approximately EUR10m in upfront and near-term payments through a combination of cash and an interest in a newly established subsidiary, alongside more than EUR100m in regulatory and commercial sales milestones. The proposed deal also includes royalties of 8% to 10% on sales projected by TME Pharma to peak at approximately USD1bn, as well as a share of sublicensing fees.
TMS plans to establish a subsidiary to facilitate financing and further clinical development of NOX-A12, with TME Pharma supporting development as a partner and minority shareholder.
The companies aim to finalise a definitive agreement to enable the rapid resumption of the Phase 2 GLORIA study evaluating NOX-A12 for glioblastoma.
NOX-A12 has received Fast Track designation from the US Food and Drug Administration (FDA) and Orphan Drug designations in the United States and Europe. Clinical results from the GLORIA study have been published in Nature Communications.
The proposed financial terms remain subject to further negotiations and the signing of a definitive agreement.
Cumberland Pharmaceuticals to submit New Drug Application for ifetroban
Lynch Regenerative Medicine's Phase IIb clinical trial of rhPDGF-BB injection cleared by FDA
European Commission approves Novartis' Cosentyx for polymyalgia rheumatica
Edwards Lifesciences wins FDA approval for PASCAL Precision tricuspid repair system
GSK wins US FDA approval for chronic hepatitis B treatment Hibsago
Solventum's combined use of Restrata Matrix and Solventum VAC Therapy receives FDA 510(k) clearance
Viatris' RYZUMVI receives US FDA Approval to treat presbyopia
Omeros receives negative EU opinion on narsoplimab after re-examination
Ionis' TRYNGOLZA recommended for EU approval in severe hypertriglyceridemia
FDA approves Genentech's Enspryng as first at-home subcutaneous treatment for thyroid eye disease
EMA issues positive CHMP opinion for Revolution Medicines' RASONQUE in metastatic pancreatic cancer