Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AD-209-1B is a specific dose formulation of AD-209, an investigational triple fixed-dose combination (FDC) therapy developed by Addpharma Inc. for the treatment of essential hypertension. It contains three active ingredients: amlodipine (a calcium channel blocker), chlorthalidone (a thiazide-like diuretic), and telmisartan (an angiotensin II receptor blocker). This combination targets multiple pathways of blood pressure regulation, including the renin-angiotensin-aldosterone system, calcium-mediated vascular contraction, and renal sodium reabsorption. It is classified as an incrementally modified drug (IMD) in South Korea and is administered orally as a film-coated tablet. The drug aims to provide superior blood pressure control compared to dual therapies by combining complementary mechanisms of action.
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 AD-209-1B.