drugset / Trial / NCT05999799
A Dose Finding Study to Investigate the Safety and Effectiveness of GSK1070806 in Adult Participants With Moderate to Severe Atopic Dermatitis
RandomizedParallel-groupDouble-blindTreatment
Summary
This study is parallel group, placebo-controlled dose-ranging study to evaluate the efficacy, safety, pharmacokinetics, and pharmacodynamics of GSK1070806 in adult participants with moderate to severe Atopic Dermatitis (AtD), who have previously been treated with medicated topical treatments or a biologic therapy.
Timeline
- Start
- 2023-11-16
- Primary completion
- 2025-07-23
- Completion
- 2025-07-23
Outcome
Outcome not reported
Stopped (Business): “Sponsor decision to early terminate the study based on the pre-defined futility criterion for efficacy. No safety concerns were identified.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GSK1070806 | Monoclonal antibody | — | Subcutaneous |