Study S002789
A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of GZR18 Injection in Healthy Subjects Following Single Dose and Once-weekly Dose for 2 Consecutive Weeks Until Reaching the Target Dose
Registration
Registered primary outcomes
- TEAE [after 28/35 days of treatment]
Linked records (0)
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