Biopharma Transcript

Biodexa Pharmaceuticals Plc BDRX

Nasdaq · Phase 3 · oncology · small molecule · EDGAR · Updated Oct 24, 2026

Biodexa Pharmaceuticals Plc (Nasdaq: BDRX) is an oncology drug developer. Its lead program, eRapa, is in Phase 3 for Familial adenomatous polyposis (FAP). Its next catalyst on record is eRapa: Biodexa announces the pre-specified futility analysis for its Serenta Phase 3 trial of eRapa in FAP could take place early next year with database lock potentially occurring around the end of next year. (H1 2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: eRapa — Biodexa announces the pre-specified futility analysis for its Serenta Phase 3 trial of eRapa in FAP could take place early next year with database lock potentially occurring around the end of next year. (H1 2027). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
eRapaFamilial adenomatous polyposis (FAP)small moleculePhase 3
eRapaNon-muscle invasive bladder cancer (NMIBC)small moleculePhase 2
MTX240 (OPB-171775)GISTsmall moleculePre-clinical

Recent results and decisions

  1. Oct 14, 2026
    completed enrollment Biodexa enrolled 100 patients in its registrational Phase 3 trial of eRapa in FAP (Serenta trial).Enrolment of the 100th patient represents an important milestone for Serenta and reflects the continued strong recruitment performance across our participating sites. Filing
  2. Oct 13, 2026
    completed enrollment Biodexa enrolled 100 patients in its registrational Phase 3 Serenta trial of eRapa in FAP.Biodexa Pharmaceuticals PLC is pleased to announce that it has enrolled 100 patients in its registrational Phase 3 trial of eRapa in Familial Adenomatous Polyposis (FAP). Filing
  3. Nov 3, 2025
    approval EMA approved the CTA for the Phase 3 Serenta trial in FAP (Denmark, Germany, Netherlands, Spain); ex-US regulatory action.announced the approval of a Clinical Trial Application (CTA) by the European Medicines Agency (EMA) of its pivotal Phase 3 Serenta trial in patients with familial adenomatous polyposis (FAP) Filing

For subscribers

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