Stapokibart for moderate-to-severe seasonal allergic rhinitis: a randomized phase 3 trial
Release date:
2025-03-06
Description:
The study was a phase 3 multicenter, randomized, double-blind, placebo-controlled clinical trial with 108 patients diagnosed with moderate-to-severe SAR. Participants were randomized to receive subcutaneous stapokibart 600 (loading does)-300 mg or placebo every 2 weeks for 4 weeks. The primary endpoint was mean change from baseline in daily reflective total nasal symptom score (rTNSS) over first 2 weeks.
For each controlled access study, there is a corresponding Data Access Committee(DAC) to determine the access permissions. Access to actual data files is not managed by NGDC.
Organization: Beijing Tongren Hospital, Capital Medical University
Submission date: 2024-12-30
Requests: -
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