Study S000342
A Phase 1 Clinical Trial to Assess the Safety of DWRX5003 and Relative Bioavailability to DWC202502 and DWC202503 in Healthy Adult Volunteers
Registration
Registered primary outcomes
- AUC 0-t [Pre-dose (0 hour) up to 672 hours post-dose]
- Cmax [Pre-dose (0 hour) up to 672 hours post-dose]
Linked records (0)
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