Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Amlodipine besylate + losartan potassium is a fixed-dose combination (FDC) antihypertensive medication. It combines amlodipine besylate, a long-acting dihydropyridine calcium channel blocker (CCB), with losartan potassium, an angiotensin II receptor blocker (ARB). Amlodipine works by inhibiting the influx of calcium ions into vascular smooth muscle and cardiac muscle cells, resulting in peripheral vasodilation and reduced blood pressure. Losartan selectively blocks the binding of angiotensin II to the AT1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland, thereby blocking the vasoconstrictor and aldosterone-secreting effects of angiotensin II. This combination is developed by Beijing Hanmi Pharmaceutical for the treatment of primary mild to moderate hypertension, particularly in patients whose blood pressure is not adequately controlled by monotherapy.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on amlodipine besylate + losartan potassium.