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Vascace (CILAZAPRIL)
Vascace (generic name: CILAZAPRIL) is a cilazapril drug. It is currently in Phase 2 development for Hypertensive disorder.
Cilazapril blocks the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor.
Vascace is a small molecule inhibitor of the angiotensin-converting enzyme. It works by inhibiting the angiotensin-converting enzyme, which is involved in blood pressure regulation.
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Baseline phase 2 → approval rate
+15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% 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.
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2031–2034 | — |
| EMA | EU | 2032–2035 | +0.7 yr |
| MHRA | GB | 2032–2035 | +0.7 yr |
| Health Canada | CA | 2032–2036 | +0.9 yr |
| TGA | AU | 2032–2036 | +1.2 yr |
| PMDA | JP | 2032–2036 | +1.5 yr |
| NMPA | CN | 2033–2037 | +2.3 yr |
| MFDS | KR | 2032–2036 | +1.4 yr |
| CDSCO | IN | 2032–2037 | +1.8 yr |
| ANVISA | BR | 2033–2037 | +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 name | CILAZAPRIL |
|---|---|
| Drug class | cilazapril |
| Target | Angiotensin-converting enzyme |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | Phase 2 |
Mechanism of action
Imagine your blood vessels are like roads in a city. Angiotensin II is like a traffic cop that makes the roads narrower, increasing blood pressure. Cilazapril removes this traffic cop, allowing the roads to stay open and blood pressure to decrease.
Approved indications
- Hypertensive disorder
Common side effects
- Amaurosis fugax
- Urinary tract disorder
- Ocular discomfort
- Haemorrhagic stroke
- Head discomfort
- Tinnitus
- Generalised oedema
- Photophobia
- Altered state of consciousness
- Blindness
- Diplopia
- Presyncope
Key clinical trials
- Association of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers With Post-Stroke Pneumonia: A Real-World Retrospective Cohort Study
- NT-proBNP Selected Prevention of Cardiac Events in Diabetic Patients (PHASE4)
- Optimalization of Nephroprotection Using Agents Inhibiting Renin-Angiotensin-Aldosterone System (NA)
- ACEi/ARB Alone Versus ACEi/ARB Plus Steroids in the Treatment of Primary IgA Nephropathy, a RCT (NA)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- Vascace CI brief — competitive landscape report
- Vascace updates RSS · CI watch RSS
Frequently asked questions about Vascace
What is Vascace?
How does Vascace work?
What is Vascace used for?
What is the generic name of Vascace?
What drug class is Vascace in?
What development phase is Vascace in?
What are the side effects of Vascace?
What does Vascace target?
Related
- Drug class: All cilazapril drugs
- Target: All drugs targeting Angiotensin-converting enzyme
- Therapeutic area: All drugs in Cardiovascular
- Indication: Drugs for Hypertensive disorder
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing