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Not yet recruiting Phase 1 NCT06897813

A Phase I Randomised, Double-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Food Effect of WD-910 in Healthy Participants

Phase 1 – testing safety in a small group of people
Conditions: Healthy Participants

Sponsor: Zhejiang Wenda Pharma Technology LTD.

trial.available_in: БГ
Overview
This is a phase I, randomised, double-blind, placebo-controlled, 3-part study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and food effect of WD-910 in in Healthy Participants Detailed
Who can participate
Inclusion Criteria: * Aged 18 to 55 years (inclusive) at the time of informed consent. * Body mass index (BMI) between 18 to 32 kg/m2 and male participant with body weight of ≥ 50.0 kg, female participant with body weight ≥ 45.0 kg Exclusion Criteria: * Any major surgery within 12 weeks prior to Day 1, or any planned surgery during the study. * Poor pill swallowing ability
Locations 1
Australia (1)
Nucleus Network Pty Ltd
Melbourne , Victoria
Technical details
Status
Not yet recruiting
Phase
Phase 1
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
55 Years
Healthy volunteers
No
Start date
30.06.2025
Completion date
31.12.2025
Registry ID
NCT06897813
Source
anzctr
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