Equilibra Bioscience

Equilibra Bioscience

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Private Company

Total funding raised: $3.8M

Overview

Equilibra Bioscience is a private, clinical-stage biotech advancing SR604, a novel anti-APC monoclonal antibody, as a potential treatment for hemophilia and other bleeding disorders. The company has initiated a Phase 1 clinical trial (NCT06349473) following U.S. FDA IND clearance and has secured Orphan Drug Designation for SR604 in hemophilia A and B. Its approach aims to rebalance the coagulation cascade by inhibiting the natural anticoagulant protein APC, offering a new mechanism of action for patients, including those with inhibitors.

HematologyBleeding Disorders

Technology Platform

Discovery and development of monoclonal antibodies targeting the activated Protein C (APC) pathway to rebalance the coagulation cascade in bleeding disorders.

Funding History

1
Total raised:$3.8M
Seed$3.8M

Opportunities

SR604's first-in-class anti-APC mechanism addresses a high-unmet need in hemophilia, particularly for inhibitor patients.
Orphan Drug Designation provides regulatory and commercial advantages.
Positive data could attract partnership or acquisition interest from larger hematology-focused pharma companies.

Risk Factors

High clinical development risk for a novel mechanism; potential safety concerns related to thrombosis.
Significant financing risk as a private, pre-revenue company.
Intense competition in the hemophilia market from established factor and non-factor therapies.

Competitive Landscape

The hemophilia market is competitive, dominated by factor replacements (e.g., from Takeda, Sanofi, Novo Nordisk) and the non-factor therapy emicizumab (Roche). Other novel mechanisms (e.g., fitusiran, concizumab) are also in development. SR604 must differentiate on efficacy, safety, or patient population to gain market share.