Trial intelligence / Profile preview

RVP-001 in healthy adult volunteers

NCT05413668Phase 1Completed

Sponsor
Reveal Pharmaceuticals
Start
May 2022
Primary completion
Jul 2022
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial comparing RVP-001 with Placebo (2 arms). Primary endpoints: Safety and tolerability of single ascending doses, Pharmacokinetic (PK) Parameter Cmax at 120 hours and 4 more. Started May 2022; status: completed.

02

Drugs

manganese-based contrast agent RVP-001

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