Who are TAK-536CCB's main competitors?

No direct comparators detected in our index.

How often does this brief refresh?

Every 30 minutes from primary sources (FDA, EMA, MHRA, PMDA, ClinicalTrials.gov, USPTO). Subscribe to the RSS feed below for push alerts.

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Last reviewed 2026-06-10 · How we verify

TAK-536CCB — Competitive Intelligence Brief

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

TAK-536CCB (TAK-536CCB) competitive landscape: 0 comparators, recent regulatory actions, upcoming PDUFA, patent timeline. Class: Angiotensin II receptor blocker/Calcium channel blocker combination. Area: Cardiovascular.

phase 3 Angiotensin II receptor blocker/Calcium channel blocker combination Angiotensin II type 1 receptor (AT1R); L-type calcium channels Cardiovascular Small molecule Live · refreshed every 30 min

Target snapshot

TAK-536CCB (TAK-536CCB) — Takeda. TAK-536CCB is a dual angiotensin II receptor blocker and calcium channel blocker combination designed to lower blood pressure through multiple mechanisms.

Comparator set

Auto-detected by same drug class / molecular target / therapeutic area, ranked by phase + recency. Override with ?vs=slug1,slug2,….

Drug	Generic	Sponsor	Phase	Class	Target	Approval / PDUFA
TAK-536CCB TARGET	TAK-536CCB	Takeda	phase 3	Angiotensin II receptor blocker/Calcium channel blocker combination	Angiotensin II type 1 receptor (AT1R); L-type calcium channels

Recent regulatory actions (last 90 days)

No regulatory actions in the last 90 days for this set.

Upcoming PDUFA dates (next 180 days)

No PDUFA dates in the next 180 days for this set.

Patent timeline (forward window)

No upcoming patent expiries for this set.

Sponsor landscape (Angiotensin II receptor blocker/Calcium channel blocker combination class)

Takeda · 1 drug in this class

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Cite this brief

Drug Landscape (2026). TAK-536CCB — Competitive Intelligence Brief. https://druglandscape.com/ci/tak-536ccb. Accessed 2026-06-10.

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing