lonigutamab (VB421) / Pierre Fabre, ACELYRIN 
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  • ||||||||||  lonigutamab (VB421) / Pierre Fabre, ACELYRIN
    Enrollment change, Trial completion date, Trial primary completion date:  Efficacy and Safety of Lonigutamab in Subjects with Thyroid Eye Disease (TED) (clinicaltrials.gov) -  Sep 26, 2024   
    P1/2,  N=54, Recruiting, 
    N=38 --> 54 | Trial completion date: Oct 2024 --> May 2025 | Trial primary completion date: Oct 2024 --> May 2025
  • ||||||||||  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
  • ||||||||||  lonigutamab (VB421) / Pierre Fabre, ACELYRIN
    Phase classification:  Efficacy and Safety of Lonigutamab in Subjects with Thyroid Eye Disease (TED) (clinicaltrials.gov) -  Jun 18, 2023   
    P1/2,  N=38, Recruiting, 
    Trial completion date: Feb 2024 --> Oct 2024 | Trial primary completion date: Feb 2024 --> Oct 2024 Phase classification: P1b --> P1/2