Biopharma Transcript

Keros Therapeutics, Inc. KROS

Nasdaq · Phase 2 · rare genetic · protein/peptide · EDGAR · Updated Nov 6, 2026

Keros Therapeutics, Inc. (Nasdaq: KROS) is a rare genetic drug developer. Its lead program, rinvatercept (KER-065), is in Phase 2 for Duchenne muscular dystrophy (DMD). Its next catalyst on record is rinvatercept (KER-065): regulatory engagement on Phase 2 trial design in ALS (H2 2026).

Upcoming catalysts

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

Next further out: rinvatercept (KER-065) — regulatory engagement on Phase 2 trial design in ALS (H2 2026). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
elritercept (KER-050)myelodysplastic syndromes (MDS) - lower-riskprotein/peptidePhase 3
elritercept (KER-050)myelofibrosisprotein/peptidePhase 3
rinvatercept (KER-065)Duchenne muscular dystrophy (DMD)protein/peptidePhase 2
rinvatercept (KER-065)amyotrophic lateral sclerosis (ALS)protein/peptidePre-clinical

Recent results and decisions

  1. Sep 29, 2026
    started Takeda dosed first patient in ELRiSE MF, a Phase 3 trial of elritercept in myelofibrosis patients with anemia on ruxolitinib, triggering a $20 million milestone payment to Keros.The milestone marks another important step forward for the elritercept program. Filing
  2. started First patient dosed in Phase 2 clinical trial of rinvatercept in patients with Duchenne muscular dystrophy in September 2026.In September 2026, Keros announced the first patient was dosed in the Phase 2 clinical trial of rinvatercept in patients with DMD. Filing

For subscribers

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