Drug intelligence / Profile preview

amlodipine + candesartan

Development stage
Unknown
Lead developer
Takeda
Modality
Small Molecules
Administration
Oral
01

Overview

AD-103 is a fixed-dose combination (FDC) small molecule candidate developed by Addpharma, a South Korean pharmaceutical company specializing in incrementally modified drugs (IMDs). It consists of amlodipine, a dihydropyridine calcium channel blocker (CCB), and candesartan cilexetil, an angiotensin II receptor blocker (ARB). The combination is designed for the treatment of hypertension, leveraging two distinct antihypertensive mechanisms to achieve synergistic blood pressure reduction. Amlodipine acts by inhibiting the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle, leading to peripheral vasodilation. Candesartan cilexetil is a prodrug that is converted to candesartan, which selectively blocks the binding of angiotensin II to the AT1 receptor, thereby inhibiting vasoconstriction and aldosterone secretion. AD-103 is currently in Phase 1 clinical development in South Korea.

Other names
AD-103-Addpharma-CardiovascularAD103-Addpharma-CardiovascularAD 103-Addpharma-Cardiovascular
02

Targets

CACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)AGTR1 (Angiotensin II Type-1 receptor)

Beyond the preview

Go deeper on amlodipine + candesartan.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on amlodipine + candesartan.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call