Trial intelligence / Profile preview

Safety and PK/PD of SHR-3032 in Healthy Subjects

NCT06090799Phase 1Completed

Sponsor
Hengrui Therapeutics
Start
Nov 2023
Primary completion
Mar 2024
Modality
Biological product
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in graft rejection comparing SHR-3032 with Placebo (2 arms). Primary endpoints: Incidence and severity of adverse events/serious adverse events at Day 99, Pharmacokinetic parameter of SHR-3032: Cmax at Day 99 and 6 more. Started Nov 2023; status: completed.

02

Drugs

SHR-3032
03

Conditions

graft rejection

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