This is an adaptive, randomized, double-blinded, placebo-controlled, Phase II/III study conducted to evaluate the effect of SCTA01 on participant survival and clinical efficacy in participants with severe COVID-19 admitted to high dependence or ICUs. The study duration of subject participation will be up to: 120 days Participants will receive a single intravenous (IV) infusion of SCTA01 at Treatment day 1. Follow up visits will be up to 120 days or early withdrawal visit.
The study is a multicenter, adaptive, randomized, double-blinded, and placebo-controlled Phase II/III trial. It will be conducted globally. The study will evaluate the efficacy and safety of SCTA01 compared to placebo both given with BSC in participants with severe COVID-19. The subjects will be randomized by 1:1 ratio to SCTA01 and placebo group. The primary objective of the study is to evaluate participant survival from randomization to Day 29 between study group and control group. At the end of the Phase II part of the study, an interim analysis will be performed for safety run-in and futility stopping.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
560
Recombinant anti-SARS-CoV-2 spike protein monoclonal antibody
The excipients of SCTA01
All-cause mortality rate at D29
The mortality rates in placebo and treatment groups regardless of the cause of death.
Time frame: Day 29
All-cause mortality rate at Day 60
The mortality rates in placebo and treatment groups regardless of the cause of death.
Time frame: Day 60
Time to discontinue mechanical ventilation (MV) at Day 29
The number of days from randomization to discontinue MV support
Time frame: Baseline through Day 29
Time to improvement of two categories on WHO 10-Point Ordinal Scale from baseline at Day 29
The number of days from baseline to two categories decreases on World Health Organization (WHO) 10-Point Ordinal Scale at Day 29.
Time frame: Baseline through Day 29
Time to discontinue supplemental oxygen at Day 29
The number of days from randomization to discontinue supplemental oxygen support
Time frame: Baseline through Day 29
Time to hospital free at Day 29
The number of days from randomization to subject's discharge from hospital.
Time frame: Baseline through Day 29
Change from baseline in viral shedding as measured by quantitative reverse transcription polymerase chain reaction (RT-qPCR)
Change from baseline in viral shedding
Time frame: Baseline through Day 29
SAE
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SAEs collected from Day 1 to Day 120
Time frame: Day 1 through Day 120
Anti-drug antibody (ADA)
ADA will be tested at Day 29 and Day120 after SCTA01/placebo administration
Time frame: Day 29, Day 120