drugset / Trial / NCT05019040

Study of the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of PA1010 in HBV Patients

NCT05019040 ↗

Phase 1/2 Completed 36 enrolled Zhejiang Palo Alto Pharmaceuticals, Inc.
RandomizedSequentialOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic characteristics of multiple ascending dose (MAD) of PA1010 tablets in Chinese adults with Chronic Hepatitis B.

Timeline

Start
2021-09-17
Primary completion
2022-11-15
Completion
2022-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject PA1010 Unknown 5 mg —
Subject PA1010 Unknown 10 mg —
Subject PA1010 Unknown 20 mg —