Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Moexipril + hydrochlorothiazide** is an oral fixed-dose antihypertensive combination of moexipril hydrochloride, an angiotensin-converting enzyme inhibitor prodrug converted to the active metabolite moexiprilat, and hydrochlorothiazide, a thiazide diuretic. Moexiprilat inhibits angiotensin-converting enzyme, reducing angiotensin II formation, vasoconstriction, and aldosterone secretion; hydrochlorothiazide promotes renal sodium and chloride excretion through effects in the distal renal tubule. The combination was marketed as Uniretic in the United States in immediate-release tablet strengths including 7.5 mg/12.5 mg, 15 mg/12.5 mg, and 15 mg/25 mg, and is indicated for hypertension. ([accessdata.fda.gov](https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/020729s021lbl.pdf))
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 moexipril + hydrochlorothiazide.