Join this challenge to test your novel agent with the FLOT backbone in fresh gastric resection tissues, aiming to double pathological complete response (pCR) rates beyond the current ~7-19% and transform perioperative outcomes in a rapidly evolving market.
The FLOT regimen (fluorouracil, leucovorin, oxaliplatin, docetaxel) is the established perioperative standard for resectable gastric or gastroesophageal junction (GEJ) adenocarcinoma, yet pCR rates remain suboptimal—typically 7-15% with FLOT alone and up to ~19% even with recent additions like durvalumab (per MATTERHORN trial data). This leaves a significant gap in achieving deeper tumor eradication, reducing recurrence risk, and improving long-term survival in a disease with high mortality.
FUSIONx invites biotechs to nominate complementary assets (e.g., novel immunotherapies, targeted agents, or ADCs) to combine with FLOT, tested on high-volume, fresh resection specimens (stomach/lymph nodes) using our clinically validated ex-vivo platform. By capturing full human tumor microenvironment dynamics, we identify synergies that could substantially boost pCR rates, enhance event-free survival, and position the combo for guideline inclusion or rapid clinical advancement. Success here offers massive market potential in the $8B+ gastric cancer space, with strong exit appeal to innovators protecting perioperative IO or targeted pipelines.
The Investment Model:
The Logistics Flow
The Win/Win Outcomes