Evaluate the Pharmacokinetics, Safety, and Tolerability of NSHO-101 in Healthy Participants
Part of paid clinical trials in Anaheim, California.
- Sponsor
- Ensho Therapeutics, Inc.
- Study ID
- NCT07403552
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Healthy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- NSHO-101 — DRUGDose form - tablet Route of administration - oral Regimen / Treatment period - QD for 14 days
Study Details
The purpose of this study is to evaluate the pharmacokinetics, safety, and tolerability of NSHO-101 in Healthy Participants.
Key Dates
- Start date
- Jan 31, 2026
- Status verified
- Feb 2026
- Primary completion
- Mar 31, 2026
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 24 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: NSHO-101 Dose AOral dose A of NSHO-101 QD for 14 days
- Experimental: NSHO-101 Dose BOral dose B of NSHO-101 QD for 14 days
Primary Outcome Measure
Pharmacokinetics: Maximum Concentration (Cmax) [ Time Frame: Day 1 to Day 18 ]
Central Contacts
- Bittoo Kanwar, MD, MD973-314-8995
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cenexel Anaheim CA | Anaheim | California | 92801 | - |
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