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olmesartan medoxomil+probenecid
Olmesartan medoxomil blocks angiotensin II receptors to lower blood pressure, while probenecid inhibits uric acid reabsorption in the kidney to reduce serum uric acid levels.
Olmesartan medoxomil blocks angiotensin II receptors to lower blood pressure, while probenecid inhibits uric acid reabsorption in the kidney to reduce serum uric acid levels. Used for Hypertension with hyperuricemia or gout risk.
At a glance
| Generic name | olmesartan medoxomil+probenecid |
|---|---|
| Sponsor | Central South University |
| Drug class | Angiotensin II receptor blocker + uricosuric agent |
| Target | AT1 receptor (angiotensin II type 1 receptor); uric acid transporter (URAT1) |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular; Rheumatology |
| Phase | FDA-approved |
Mechanism of action
Olmesartan medoxomil is an angiotensin II receptor blocker (ARB) that reduces vasoconstriction and aldosterone secretion, thereby lowering blood pressure. Probenecid is a uricosuric agent that blocks the renal tubular reabsorption of uric acid, increasing its urinary excretion and reducing hyperuricemia. This combination addresses both hypertension and elevated uric acid levels, which may co-occur in certain patient populations.
Approved indications
- Hypertension with hyperuricemia or gout risk
Common side effects
- Dizziness
- Hyperkalemia
- Renal impairment
- Headache
- Gastrointestinal upset (probenecid-related)
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- olmesartan medoxomil+probenecid CI brief — competitive landscape report
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- Central South University portfolio CI