drugset / Trial / NCT06255834
Phase 1 Study for IPG11406 in Health Volunteer
RandomizedSequentialDouble-blindTreatment
Summary
A phase 1, randomized, double-blind, placebo-controlled, single and multiple dose escalation study to evaluate the safety, tolerability, pharmacokinetics (PK) and food effect of orally administered IPG11406 in healthy adult participants
Timeline
- Start
- 2024-02-24
- Primary completion
- 2024-12-30
- Completion
- 2024-12-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IPG11406 | Unknown | 0.5 mg | Oral |
| Subject | IPG11406 | Unknown | 2 mg | Oral |
| Subject | IPG11406 | Unknown | 6 mg | Oral |
| Subject | IPG11406 | Unknown | 10 mg | Oral |
| Subject | IPG11406 | Unknown | 20 mg | Oral |
| Subject | IPG11406 | Unknown | 40 mg | Oral |
| Subject | IPG11406 | Unknown | 80 mg | Oral |