Hemab Therapeutics Secures $157M Series C Funding to Advance Rare Blood Disorder Treatments

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Hemab Therapeutics Secures $157M Series C Funding to Advance Rare Blood Disorder Treatments

Hemab Therapeutics, a biotech company focused on developing treatments for rare and underserved bleeding disorders, has successfully raised $157 million in a Series C funding round. The financing, led by Sofinnova Partners, will support the advancement of Hemab's pipeline and clinical candidates for conditions such as Glanzmann thrombasthenia and von Willebrand disease.

Funding Details and Investor Participation

The oversubscribed Series C round saw participation from both existing and new investors. Alongside lead investor Sofinnova Partners, the funding effort included contributions from:

  • Existing investors: Novo Holdings, RA Capital Management, and Rock Springs Capital
  • New investors: Qatar Investment Authority and Avoro Capital Advisors
  • An unnamed large global asset management company

Dr. Benny Sorensen, CEO of Hemab Therapeutics, stated, "The quality of our investor syndicate and this significant financing validate our approach and enable us to continue building what we believe will become the ultimate clotting company."

Clinical Programs and Development Strategy

Hemab's clinical pipeline is centered on two key assets:

Sutacimig for Glanzmann Thrombasthenia

Sutacimig, a midstage asset, is being developed as the first prophylactic treatment for Glanzmann thrombasthenia, a rare genetic bleeding disorder. The drug candidate, a subcutaneously administered bispecific antibody, has shown promising results in Phase 2 studies, achieving clinically meaningful bleeding reduction.

  • Mechanism of action: Mimics the function of factor VIIa while targeting activated platelets at bleeding sites
  • Next steps: Planned evaluation in Factor VII deficiency in the coming year

HMB-002 for Von Willebrand Disease

HMB-002 is a monovalent antibody designed as a bleeding prophylactic for patients with von Willebrand disease. Early data indicate that the drug can directly target the underlying pathophysiology of the disease by increasing both Von Willebrand Factor and Factor VIII levels.

  • Dosing goal: Hemab is aiming for once-monthly administration
  • Future plans: The new funding will support the advancement of HMB-002 into a registration study

Expansion and Future Outlook

Hemab's ambitious growth strategy, dubbed the "1-2-5" concept, aims to advance five development projects by 2025. The company's pipeline currently lists sutacimig and HMB-002, with plans to introduce additional candidates into clinical development, including a prospect called HMB-003 in 2026.

Dr. Joe Anderson, partner at Sofinnova Partners and new board member of Hemab, highlighted the company's "deep scientific excellence and strong clinical execution," calling it a "standout company in the biotech landscape."

As Hemab continues to build its portfolio, the company emphasizes a technology-agnostic approach, selecting optimal scientific strategies for each specific condition it targets. This precision approach utilizes "targeted solutions rather than generic approaches," according to the company's website.

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