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losartan/amlodpine
Losartan/amlodipine is a fixed-dose combination medication developed by the University of Pavia for the treatment of hypertension. It combines losartan, an angiotensin II receptor blocker (ARB), and amlodipine, a calcium channel blocker, to provide a synergistic effect in lowering blood pressure. The combination aims to improve blood pressure control and reduce the need for multiple medications. However, it does not have an FDA label, indicating that it may be used off-label or is under investigation. Common side effects include dizziness (10%), peripheral edema (8%), and headache (7%). The drug is not yet commercially available, but it has the potential to offer a new option for patients with hypertension.
At a glance
| Generic name | losartan/amlodpine |
|---|---|
| Sponsor | University of Pavia |
| Drug class | Angiotensin II receptor blocker (ARB) / Calcium channel blocker (CCB) |
| Target | Angiotensin II receptors (AT1) and L-type calcium channels |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
Approved indications
Pipeline indications
Common side effects
Drug interactions
- CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin) may increase the plasma concentrations of amlodipine
- CYP3A4 inducers (e.g., rifampin, St. John's wort) may decrease the plasma concentrations of amlodipine
- Concomitant use with potassium-sparing diuretics (e.g., spironolactone, triamterene) may increase the risk of hyperkalemia
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 |