drugset / Trial / NCT04709328
To Evaluate SCTA01 Treatment of High-risk Outpatients With COVID-19
RandomizedParallel-groupTriple-blindTreatment
Summary
The study is a multicenter, adaptive, randomized, double-blinded and placebo-controlled Phase II/III clinical trial. It will be conducted at selected investigational sites globally. The study is comprised of 2 parts.
Timeline
- Start
- 2021-03-28
- Primary completion
- 2022-01-01
- Completion
- 2022-03-01
Publications
- Diaz J, Fonseca A, Yan L, Liu D, Xie L. Efficacy and safety of SARS-CoV-2 neutralizing antibody, SCTA01, in high-risk outpatients diagnosed with COVID-19: A Phase II clinical trial. Contemp Clin Trials Commun. 2025 May 17;45:101496. doi: 10.1016/j.conctc.2025.101496. eCollection 2025 Jun.
- Kreuzberger N, Hirsch C, Chai KL, Tomlinson E, Khosravi Z, Popp M, Neidhardt M, Piechotta V, Salomon S, Valk SJ, Monsef I, Schmaderer C, Wood EM, So-Osman C, Roberts DJ, McQuilten Z, Estcourt LJ, Skoetz N. SARS-CoV-2-neutralising monoclonal antibodies for treatment of COVID-19. Cochrane Database Syst Rev. 2021 Sep 2;9(9):CD013825. doi: 10.1002/14651858.CD013825.pub2.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | UPANOVIMAB | Monoclonal antibody | 750 mg | Intravenous |
| Subject | UPANOVIMAB | Monoclonal antibody | 1500 mg | Intravenous |
| Subject | UPANOVIMAB | Monoclonal antibody | 3000 mg | Intravenous |