Trials / Completed
CompletedNCT06316973
A Clinical Study to Evaluate the Safety of CS-1103 in Healthy Participants
A Phase 1a, Randomized, Double-Blind, Placebo-Controlled, Single Center Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of CS-1103 Following Single, Ascending Intravenous Dose Administration in Healthy Participants
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Clear Scientific, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this Phase 1a study is to evaluate safety, tolerability, and pharmacokinetics (PK) of single, ascending doses of CS-1103, administered by intravenous (IV) infusion in healthy participants.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | CS-1103 | CS-1103 for infusion |
| DRUG | Sterile Saline | Sterile Saline for Injection |
Timeline
- Start date
- 2024-02-07
- Primary completion
- 2024-05-30
- Completion
- 2024-06-06
- First posted
- 2024-03-19
- Last updated
- 2025-11-10
- Results posted
- 2025-11-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06316973. Inclusion in this directory is not an endorsement.