Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
placebo + remdesivir refers to the control arm of a Phase III clinical trial (NCT04645394) conducted by Daewoong Pharmaceutical Co. Ltd. to evaluate the efficacy and safety of DWJ1248 (camostat mesylate) in patients with severe COVID-19. In this arm, patients receive an oral placebo alongside intravenous remdesivir, which serves as the standard-of-care comparator. Remdesivir is a nucleotide analog prodrug that, once metabolized into its active triphosphate form, competes with adenosine triphosphate for incorporation into the viral RNA strand by the SARS-CoV-2 RNA-directed RNA polymerase (RdRp). This incorporation leads to delayed chain termination during viral RNA replication, effectively inhibiting the spread of the virus within the host. The placebo component is an inactive oral tablet designed to match the appearance and administration schedule of camostat mesylate.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on placebo + remdesivir.