Placebo
DrugParticipants will receive placebo.
NCT Number: NCT07160608
The primary objective of this study is to evaluate the safety and tolerability of tarperprumig in participants with newly diagnosed or relapsing anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis.
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Phase 2
Research Site, Ciudad de Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive placebo.
Participants will receive tarperprumig.
Other names: ALXN1820
Time frame: Baseline through Week 70
Time frame: Week 26
Time frame: Week 52
Time frame: Baseline through Week 52
Time frame: Week 26 through Week 70
Time frame: Week 26 through Week 70
Time frame: Baseline, Weeks 26, and 52
Time frame: Baseline through Week 52
Time frame: Baseline, Weeks 26, and 52
Time frame: Baseline, Weeks 26, and 52
Time frame: Baseline, Weeks 26, and 52
Time frame: Baseline, Weeks 26, and 52
Time frame: Baseline, Weeks 26, and 52
Contact information is provided by the study sponsor or research team.
Alexion Pharmaceuticals, Inc.
Industry
Phase 2, Randomized, Double-Blind, Placebo-controlled, Parallel-Group, Multicenter Study to Evaluate the Safety and Efficacy of Tarperprumig in Adult Participants With Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis (I TRANSCEND)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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