A Phase IIb, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Multidose, 24-Week Study to Evaluate the Efficacy and Safety of Atacicept in Subjects With Systemic Lupus Erythematosus (SLE)
Latest Information Update: 07 Nov 2021
At a glance
- Drugs Atacicept (Primary)
- Indications Systemic lupus erythematosus
- Focus Therapeutic Use
- Acronyms ADDRESS-II
- Sponsors EMD Serono; Merck KGaA
- 27 Feb 2020 Post hoc analysis results evaluating the treat-to-target (T2T) endpoints, published in the Rheumatology
- 24 Oct 2018 Results of integrated non-clinical and clinical data to determine an appropriate atacicept dose for a Phase 3 (P3) study; NCT00624338 and NCT01972568, presented at the 82nd American College of Rheumatology and the 52nd Association of Rheumatology Health Professionals Annual Scientific Meeting
- 24 Oct 2018 Results of post-hoc analysis of data from ADDRESS II and its long-term extension describing 48-week low disease activity and remission rates, presented at the 82nd American College of Rheumatology and the 52nd Association of Rheumatology Health Professionals Annual Scientific Meeting.