drugset / Trial / NCT07433556
Safety, Tolerability, Pharmacokinetic and Pharmacodynamic of IY-828026 in Healthy Volunteers
RandomizedParallel-groupDouble-blindTreatment
Summary
A randomized, double-blinded, partial-open, placebo/active-controlled, single/multiple dosing, dose escalation phase 1 clinical trial to evaluate the safety, tolerability, pharmacokinetic, and pharmacodynamic characteristics of IY-828026 in healthy adult volunteers
Timeline
- Start
- 2026-03-23
- Primary completion
- 2027-03
- Completion
- 2027-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IY-828026 | Unknown | 10 mg | Oral |
| Subject | IY-828026 | Unknown | 20 mg | Oral |
| Subject | IY-828026 | Unknown | 40 mg | Oral |
| Subject | IY-828026 | Unknown | 80 mg | Oral |
| Subject | IY-828026 | Unknown | 160 mg | Oral |
| Comparator | IY-828026A | Unknown | 40 mg | Oral |
| Comparator | IY-828026B | Unknown | 50 mg | Oral |
Indications
No indication recorded.