- |||||||||| lonigutamab (VB421) / Pierre Fabre, ACELYRIN
A Phase 1/2 Proof of Concept Study of Subcutaneous Lonigutamab (Anti (South Level 1 Lobby: STATION 1) - Sep 24, 2024 - Abstract #AAO2024AAO_1296; P1/2 Patients achieved clinical responses early that were maintained over the time points evaluated, including Week 12 off-treatment, supporting the potential for longer dosing intervals. Evidence from cohort 1 indicates that Loni was well tolerated and displayed clinical efficacy responses, which is further supported by cohort 2 data.
- |||||||||| lonigutamab (VB421) / Pierre Fabre, ACELYRIN
Trial completion date, Trial primary completion date: Efficacy and Safety of Lonigutamab in Subjects with Thyroid Eye Disease (TED) (clinicaltrials.gov) - Mar 22, 2024 P1/2, N=38, Recruiting, Evidence from cohort 1 indicates that Loni was well tolerated and displayed clinical efficacy responses, which is further supported by cohort 2 data. Trial completion date: Feb 2024 --> Oct 2024 | Trial primary completion date: Feb 2024 --> Oct 2024
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