A Trial Evaluating Safety, Tolerability and Efficacy of CTX340 in Participants With Hypertension
Part of paid clinical trials in Port Orange, Florida.
- Sponsor
- CRISPR Therapeutics AG
- Study ID
- NCT07758634
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- CTX340 — DRUGCTX340 is an in vivo gene editing therapy designed to utilize clustered regularly interspaced short palindromic repeats-CRISPR-associated protein 9 (CRISPR-Cas9) to target and disrupt human angiotensinogen (AGT) gene in liver.
- Placebo — DRUGOne of the arms in Phase 2 will be placebo.
Study Details
A Study of CTX340 in Participants with Uncontrolled Hypertension.
Key Dates
- First listed
- Aug 11, 2026
- Start date
- Aug 8, 2026
- Status verified
- Aug 2026
- Primary completion
- Jul 1, 2028
- Completion
- Jul 1, 2029
Study Design
- Enrollment
- 69 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Phase 1: CTX340Phase 1 is An Open-Label, Ascending Dose Design.
- Experimental: Phase 2: Recommended Phase 2 Dose CTX340Phase 2: Recommended Phase 2 Dose CTX340.
- Experimental: Phase 2: PlaceboPhase 2: Placebo.
Primary Outcome Measure
Phase 1: Incidence of dose-limiting toxicities (DLTs) [ Time Frame: Up to 12 months ]
Central Contacts
- Clinical Trials877-214-4634
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Research Site 1 | Port Orange | Florida | 32127 | - |
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