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A Phase I Study of HW241045 in Healthy Subjects

HW241045 Formulation A · Phase 1

Registry ID
NCT07593690
Phase
Phase 1
Status
Not yet recruiting
Drug / intervention
HW241045 Formulation A
Sponsor
Hubei Bio-Pharmaceutical Industrial Technological Institute Inc.
Start
2026-06
Enrollment
102
Locations
1

About this trial

This is a Phase I, randomized, double-blind, placebo-controlled study to assess the safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD), and food effect (FE) of HW241045 in healthy participants. This study consists of three parts:1)Part A: A single-dose, two-period, two-way crossover design to evaluate the safety and pharmacokinetic differences between Formulation A and Formulation B of HW241045 tablets; 2)Part B: A single-dose ascending dose design to evaluate the safety, tolerability, and pharmacokinetic profiles of HW241045 Formulation B following single administration. A food-effect study is nested within this part.3)Part C: A multiple-dose ascending dose design to evaluate the safety, tolerability, and pharmacokinetic profiles of HW241045 Formulation B after multiple administrations.

View NCT07593690 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT07593690 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.