Rallybio Corporation announced positive results from its Phase 1 confirmatory pharmacokinetic/pharmacodynamic clinical trial evaluating RLYB116, a once-weekly, subcutaneously injected C5 inhibitor in development for complement-mediated diseases, including immune platelet transfusion refractoriness (PTR) and refractory antiphospholipid syndrome (APS). The results demonstrated complete and sustained inhibition of terminal complement at the 300 mg dose, with a safety profile consistent with other subcutaneous biologics. The Phase 1 results have been announced and support plans to proceed to a Phase 2 proof of concept study in immune PTR in the second half of 2026.
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