Last reviewed 2026-05-28 · How we verify

Revelisa

Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health · Phase 2 active Small molecule ✓ Verified May 2026

Revelisa is a Small molecule drug developed by Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health. It is currently in Phase 2 development.

Revelisa is an intervention used in the treatment of acute ischemic stroke during intravenous thrombolytic therapy with alteplase. It is being studied in the context of the Russian Prospective Multicenter Registry Study of Intravenous Thrombolytic Therapy for Acute Ischemic Stroke.

Likelihood of approval

15.3% vs 15.3% industry baseline

If approved by FDA: likely 2031–2034

Steps remaining: Phase 3 → NDA/BLA submission

Confidence: Medium

Why this estimate

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).

Predicted approval windows by jurisdiction (conditional on FDA approval)

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	Revelisa
Sponsor	Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health
Modality	Small molecule
Therapeutic area	Other
Phase	Phase 2

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Russian Prospective Multicenter Registry Study of Intravenous Thrombolytic Therapy for Acute Ischemic Stroke

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:

Revelisa CI brief — competitive landscape report
Revelisa updates RSS · CI watch RSS
Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health portfolio CI

Frequently asked questions about Revelisa

What is Revelisa?

Revelisa is a Small molecule drug developed by Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health.

Who makes Revelisa?

Revelisa is developed by Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health (see full Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health pipeline at /company/federal-center-of-cerebrovascular-pathology-and-stroke-russian-federation-minist).

What development phase is Revelisa in?

Revelisa is in Phase 2.

Manufacturer: Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health — full pipeline
Therapeutic area: All drugs in Other

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