Efficacy and Safety of Novel Treatment Options for Adults With COVID-19 Pneumonia

Summary

CCAP is an investigator-initiated multicentre, randomized, double blinded, placebo-controlled trial, which aims to assess the safety and efficacy of treatment with convalescent plasma for patients with moderate-severe COVID-19. Participants will be randomized 2:1 to two parallel treatment arms: Convalescent plasma, and intravenous placebo. Primary outcome is a composite endpoint of all-cause mortality or need of invasive mechanical ventilation up to 28 days.

Timeline

Start

2020-05-01

Primary completion

2021-03-16

Completion

2021-03-16

Publications

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Drugs

Indications