The study is a multicenter, adaptive, randomized, double-blinded and placebo-controlled Phase II/III trial, and will be conducted globally. The study is comprised of two parts: dose selection (Phase II) and pivotal treatment effect (Phase III).
In this study, Phase II part will evaluate the efficacy, safety and PK of SCTA01 low dose+BSC, high dose+BSC and placebo+BSC in patients with severe COVID-19. In Phase II part, subjects will be randomized at 1:1:1 ratio. At the end of Phase II part, a dose for the Phase III will be determined. The Phase III part will evaluate the efficacy, safety, and immunogenicity of SCTA01 at the recommended dose recommended. Subjects in Phase III part will be randomized at 1:1 ratio to SCTA01+BSC and placebo+BSC groups.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
102
SCT study site
Somers Point, New Jersey, United States
SCT study site
Buenos Aires, Argentina
SCT study site
Uberlândia, Brazil
SCT study site
Talca, Chile
Time to Clinical Improvement up to Day 29
The median time to clinical improvement in the SCTA01 groups and control group
Time frame: Day 29
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SCT study site
Rionegro, Colombia
SCT study site
Monterrey, Mexico
SCT study site
Lima, Peru