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Alindapril (DELAPRIL)

Phase 3 active Small molecule

Alindapril (generic name: DELAPRIL) is a delapril drug. It is currently in Phase 3 development for Hypertensive disorder.

Delapril works by blocking the action of angiotensin-converting enzyme, a protein that constricts blood vessels.

Alindapril, also known as Delapril, is a small molecule drug that targets the angiotensin-converting enzyme (ACE). It belongs to the delapril class and is used to treat hypertensive disorders. The commercial status of Delapril is unclear, but it is likely to be patented or off-patent. Delapril has a bioavailability of 55%, but its half-life and generic manufacturers are unknown. As a result, its FDA approval status and off-patent status are also unclear.

Likelihood of approval
56.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Cardiovascular Phase 3 risk -2.0pp
    Modern cardiovascular outcome trials are large + long; many fail to beat aggressive standard-of-care.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameDELAPRIL
Drug classdelapril
TargetAngiotensin-converting enzyme
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 3

Mechanism of action

Think of your blood vessels like roads in a city. When the angiotensin-converting enzyme is active, it's like a traffic cop directing more traffic onto the roads, making them narrower and harder to pass through. Delapril blocks this traffic cop, allowing the roads to stay open and blood to flow more easily.

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Alindapril

What is Alindapril?

Alindapril (DELAPRIL) is a delapril drug, indicated for Hypertensive disorder.

How does Alindapril work?

Delapril works by blocking the action of angiotensin-converting enzyme, a protein that constricts blood vessels.

What is Alindapril used for?

Alindapril is indicated for Hypertensive disorder.

What is the generic name of Alindapril?

DELAPRIL is the generic (nonproprietary) name of Alindapril.

What drug class is Alindapril in?

Alindapril belongs to the delapril class. See all delapril drugs at /class/delapril.

What development phase is Alindapril in?

Alindapril is in Phase 3.

What does Alindapril target?

Alindapril targets Angiotensin-converting enzyme and is a delapril.

Related

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