New trial + clinical hiring Started a Phase 2 trial (NCT07704099, actual start Sep 25, 2026); since then posted 1 clinical-operations role. ClinicalTrials.gov NCT07704099 (Sep 25, 2026)Evidence (1 event)
Sep 25, 2026 · ClinicalTrials.gov NCT07704099 leadSponsor.name='Keros Therapeutics, Inc.'; phases=['PHASE2']; overallStatus=RECRUITING; startDateStruct={date:2026-09-25,type:ACTUAL}; studyFirstPostDate=2026-07-15; briefTitle='Safety and Efficacy of KER-065 in Participants With Duchenne Muscular Dystrophy'
Board tracked Radar started tracking this company’s job board (19 open jobs at last check). source ↗
Trial start Phase 2: Safety and Efficacy of KER-065 in Participants With Duchenne Muscular Dystrophy source ↗
Partnership Partnership / licensing announced Mar 9, 2026. Source: SEC filing. source ↗
Partnership Partnership / licensing: $200M (upfront, as published), announced Jan 21, 2025. Source: SEC filing. source ↗
Partnership Partnership / licensing: $200M (upfront, as published), announced Dec 3, 2024. Source: SEC filing. source ↗
Trial start Phase 2: A Study to Evaluate the Safety and Preliminary Efficacy of a Response-guided Dose Titration of KER-047 in the Treatment of Functional IDA (Iron Deficiency Anemia). source ↗
Trial start Phase 2: A Study to Investigate the Safety and Efficacy of KER-012 in Combination With Background Therapy in Adult Participants With Pulmonary Arterial Hypertension (PAH) (TROPOS Study). source ↗
Upcoming milestones
Aug 26, 2028 (ESTIMATED) · Phase 2 · Safety and Efficacy of KER-065 in Participants With Duchenne Muscular Dystrophy · NCT07704099
Estimated primary completion per ClinicalTrials.gov. Dates move.
Level (Entry/Mid/Senior/Executive) is estimated from the job title and required years of experience. Descriptions are short excerpts (about the first 60 words) of the posting plus skills picked out of it; use Read full posting for the complete text.
Funding
Last 2 years.
Partnership / licensing announced Mar 9, 2026. Source: SEC filing. source ↗
Partnership / licensing: $200M (upfront, as published), announced Jan 21, 2025. Source: SEC filing. source ↗
Partnership / licensing: $200M (upfront, as published), announced Dec 3, 2024. Source: SEC filing. source ↗
A Study to Investigate the Safety and Efficacy of KER-012 in Combination With Background Therapy in Adult Participants With Pulmonary Arterial Hypertension (PAH) (TROPOS Study).
A Study to Evaluate the Safety and Preliminary Efficacy of a Response-guided Dose Titration of KER-047 in the Treatment of Functional IDA (Iron Deficiency Anemia).
Phase 2
Withdrawn
Nov 30, 2023
Aug 29, 2025 (estimated)
Raises and investors new
Form D raises come from the company’s own SEC filing (last 2 years).
InvestorListed in the portfolio of OrbiMed (captured Oct 12, 2026). portfolio page ↗