A Study to Evaluate the Efficacy and Safety of Veverimer for the Treatment of Metabolic Acidosis
Part of paid clinical trials in Chula Vista, California.
- Sponsor
- Renibus Therapeutics, Inc.
- Study ID
- NCT07355062
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- CKD
- Metabolic Acidosis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Veverimer — DRUGGroup 1: 9 g veverimer BID
- Placebo — DRUGGroup 2: 9 g PBO BID
Study Details
The purpose of this 264 week study is is to evaluate the efficacy and safety of veverimer in treating adults with moderate-to-severe chronic kidney disease (CKD) and metabolic acidosis.
Key Dates
- First listed
- Jan 21, 2026
- Start date
- Jan 13, 2026
- Status verified
- May 2026
- Primary completion
- Jun 30, 2027
- Completion
- Jun 30, 2027
Study Design
- Enrollment
- 150 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Veverimer
- Placebo Comparator: Placebo
Primary Outcome Measure
Efficacy of Veverimer by measuring change in serum bicarbonate concentration (SBC) [ Time Frame: Visits: Screening to Day 168 ]
Central Contacts
- Ayla Rasmussen443-569-9228
Locations (21)
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California Institute of Renal Research· Chula Vista, CAAcademic Medical Research Institute· Los Angeles, CAUC Davis Health, Dept of Internal Medicine· Sacramento, CACalifornia Institute of Renal Research - San Diego· San Diego, CARenal Research Office, University of Colorado Anschutz Medical Campus· Aurora, COVelocity Clinical Research· Edgewater, FL
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