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Affibody’s licensee Rallybio Announces Positive Data for RLYB116 Phase 1 Study Demonstrating Complete and Sustained Inhibition of Terminal Complement
Regulatory
February 17, 2026
Stockholm, Sweden, February 17, 2026. Affibody’s licensee Rallybio Corporation (Rallybio) has today announced positive results from its Phase 1 confirmatory pharmacokinetic/pharmacodynamic (PK/PD) clinical study evaluating RLYB116, an innovative, once-weekly, small volume, subcutaneously injected complement factor 5 (C5) inhibitor, based on the Affibody® platform. Rallybio is developing RLYB116 for patients with complement-mediated diseases with its initial focus on immune platelet transfusion refractoriness (PTR) and refractory antiphospholipid syndrome (APS).
The data announced by Rallybio demonstrated the following:
- A 300 mg once-a-week dose of subcutaneously administered RLYB116 achieved complete and sustained inhibition of terminal complement.
- Complete and sustained inhibition of ex-vivo hemolytic activity demonstrates clinically effective blockade of terminal complement.
- RLYB116 administered as a 150 mg and 300 mg once-a-week dose was well tolerated with no gastrointestinal side effects reported among participants. The most common adverse events in both cohorts were mild-to-moderate injection site reactions, consistent with other subcutaneously administered biologics. None were severe or caused discontinuation of study drug. These results further validate the manufacturing process enhancements designed to improve the tolerability profile of RLYB116.
“We are very pleased with the highly encouraging results demonstrating complete and sustained inhibition of terminal complement by RLYB116 using a convenient, small volume, once‑weekly subcutaneous dosing,” said David Bejker, CEO of Affibody. “These data further illustrate the potential of the Affibody® platform to deliver best-in-class therapies.”
The single-blind multiple ascending dose Phase 1 confirmatory PK/PD study of RLYB116 (NCT06797375) was designed to demonstrate complete and sustained complement inhibition with favorable tolerability in healthy volunteers. The study evaluated a 4-week treatment duration that included two cohorts of eight participants each, randomized 3-to-1 to receive either RLYB116 or placebo once weekly. Cohort 1 evaluated dosing of 150 mg and Cohort 2 evaluated dosing of 300 mg. The study included a 10-week follow-up period after the conclusion of treatment.
Rallybio is currently planning to initiate a Phase 2 clinical study with RLYB116 in PTR in H2 2026 with potential for topline data in 2027.