Stock Markets June 26, 2026 10:51 AM

Hemab Therapeutics Shares Rise After Multiple ISTH Data Presentations Announced

Clinical-stage company to present first-in-human and long-term data across haemostasis pipeline at ISTH 2026 in Paris

By Maya Rios
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COAG

Hemab Therapeutics (NASDAQ: COAG) shares climbed 10.5% after the company disclosed it will present nine abstracts at the International Society on Thrombosis and Haemostasis 2026 Congress in Paris, July 11-15, 2026. The presentations will cover first-in-human results for HMB-002 in Von Willebrand disease, long-term extension outcomes for sutacimig in Glanzmann thrombasthenia, preclinical data for HMB-003, and other pipeline updates. Several programs are moving toward later-stage testing, with multiple dose assessments and Phase 3 starts planned in the second half of 2026.

Hemab Therapeutics Shares Rise After Multiple ISTH Data Presentations Announced
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Key Points

  • Hemab Therapeutics stock rose 10.5% after announcing nine presentations at the ISTH 2026 Congress in Paris (July 11-15, 2026).
  • Presentations include first-in-human HMB-002 data showing increases in Von Willebrand Factor and Factor VIII, long-term sutacimig data showing sustained reductions in treated bleeding rate, and preclinical results for HMB-003.
  • Several programs are advancing toward later-stage testing: multiple dose assessment for HMB-002 is underway, sutacimig Phase 3 studies are planned for the second half of 2026, and HMB-003 first-in-human studies are planned for H2 2026.

Hemab Therapeutics Holdings (NASDAQ: COAG) saw its stock gain 10.5% on Friday after announcing that it will present nine separate items of scientific data at the International Society on Thrombosis and Haemostasis (ISTH) 2026 Congress, scheduled for July 11-15, 2026 in Paris.

The clinical-stage biotechnology firm, with operations in Cambridge, Massachusetts and Copenhagen, will use the conference to display new results spanning its portfolio of therapies aimed at blood coagulation disorders. The planned presentations include first-in-human findings for HMB-002 in Von Willebrand disease, long-term extension data for sutacimig in Glanzmann thrombasthenia, and preclinical results for a recently disclosed program, HMB-003.

HMB-002's first-in-human dataset provided proof of mechanism in Von Willebrand disease, demonstrating increases in Von Willebrand Factor and Factor VIII following subcutaneous dosing. The company reports that a multiple dose assessment of HMB-002 is currently underway.

Hemab described HMB-003 as a peptide plasmin inhibitor developed to act as an antifibrinolytic agent to reduce bleeding. The company intends to begin first-in-human studies for HMB-003 in the second half of 2026 and to prepare clinical evaluations in heavy menstrual bleeding during 2027.

Long-term extension data for sutacimig indicated a sustained reduction in the annualized treated bleeding rate among patients with Glanzmann thrombasthenia. Regulatory designations have been granted for the program - the U.S. Food and Drug Administration conferred Breakthrough Therapy designation on sutacimig, while the European Medicines Agency awarded Priority Medicines designation.

Hemab plans to start Phase 3 studies of sutacimig in the second half of 2026. The company also noted that preclinical work supporting sutacimig will underpin an expansion into treatment of Factor VII deficiency, where a Phase 2b study is currently in progress.

Taken together, the presentations at ISTH 2026 are intended to highlight progress across Hemab's pipeline of therapies targeting coagulation disorders. Several programs are advancing into additional clinical assessments or preparing to initiate human testing within the timelines the company disclosed.


Conference: International Society on Thrombosis and Haemostasis 2026 Congress, Paris, July 11-15, 2026

Key programs to be presented: HMB-002 (first-in-human, Von Willebrand disease); sutacimig (long-term extension, Glanzmann thrombasthenia; Phase 3 planned H2 2026; Phase 2b in progress for Factor VII deficiency); HMB-003 (preclinical; first-in-human planned H2 2026; heavy menstrual bleeding studies planned 2027).

Risks

  • Clinical development timelines remain subject to change - planned starts for first-in-human studies and Phase 3 trials are future intentions and not guaranteed.
  • Ongoing and future studies (multiple dose assessment for HMB-002, Phase 3 for sutacimig, Phase 2b for Factor VII deficiency) mean program outcomes are not yet determined and remain dependent on clinical results.
  • Regulatory milestones are not final approvals - while sutacimig has received Breakthrough Therapy and Priority Medicines designations, further data and regulatory review will be required before marketing authorization.

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