Biopharma Transcript

Immuron Ltd IMRN

Nasdaq · Phase 2 · infectious disease · antibody · EDGAR · Updated Nov 4, 2026

Immuron Ltd (Nasdaq: IMRN) is an infectious disease drug developer. Its lead program, Travelan (IMM-124E), is in Phase 2 for Prevention of travelers' diarrhea (ETEC).

Upcoming catalysts

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

Pipeline

ProgramIndicationModalityStage
Travelan (IMM-124E), oral polyclonal bovine antibodyTravelers' diarrhea prophylaxis (BLA path planned)antibodyPhase 2
IMM-529Clostridioides difficile infection / recurrent CDIantibodyPre-clinical
ProIBS (marketed in Australia as listed medicine/medical device)IBS symptom reliefunclearNA_NON_THERAPEUTIC

Recent results and decisions

  1. Oct 28, 2026
    accepted FDA approved investigational new drug application for IMM-529, positioning it ready for Phase 2 clinical trials.IMM-529 has an investigational new drug (IND) application approved by the U.S. FDA and is ready to go into Phase 2 clinical trials Filing
  2. Oct 28, 2026
    completed enrollment Immuron completed the Travelan n=851 clinical trial in FY26.Travelan® n=851 trial completed Filing
  3. Oct 28, 2026
    completed enrollment Travelan® n=851 clinical trial has been completed, with IMM-124E now eligible for an end of Phase 2 meeting with the U.S. FDA.IMM-124E is eligible for an end of Phase 2 meeting with the U.S. FDA (indication: traveler's diarrhea) Filing

3 more on record.

For subscribers

Other phase 2 infectious disease companies