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ANG-3777

Angion Biomedica Corp · Phase 3 active Small molecule Under review Quality 0/100

ANG-3777 is a HGF mimetic Small molecule drug developed by Angion Biomedica Corp. It is currently in Phase 3 development for Diabetic kidney disease, Peripheral artery disease. Also known as: Hepatocyte growth factor mimetic, BB3.

ANG-3777 is a hepatocyte growth factor (HGF) mimetic that activates the MET receptor to promote tissue repair and regeneration.

ANG-3777 is a small molecule that acts as a hepatocyte growth factor receptor agonist. It is being studied in clinical trials for various conditions, including COVID-19 pneumonia, acute kidney injury, and hemodialysis patients.

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 nameANG-3777
Also known asHepatocyte growth factor mimetic, BB3
SponsorAngion Biomedica Corp
Drug classHGF mimetic
TargetMET receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 3

Mechanism of action

ANG-3777 is designed to mimic the biological activity of hepatocyte growth factor by binding to and activating the MET receptor tyrosine kinase. This activation promotes angiogenesis, tissue repair, and regeneration, particularly in ischemic tissues. The drug is being developed to treat conditions characterized by tissue damage and impaired vascular function.

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 ANG-3777

What is ANG-3777?

ANG-3777 is a HGF mimetic drug developed by Angion Biomedica Corp, indicated for Diabetic kidney disease, Peripheral artery disease.

How does ANG-3777 work?

ANG-3777 is a hepatocyte growth factor (HGF) mimetic that activates the MET receptor to promote tissue repair and regeneration.

What is ANG-3777 used for?

ANG-3777 is indicated for Diabetic kidney disease, Peripheral artery disease.

Who makes ANG-3777?

ANG-3777 is developed by Angion Biomedica Corp (see full Angion Biomedica Corp pipeline at /company/angion-biomedica-corp).

Is ANG-3777 also known as anything else?

ANG-3777 is also known as Hepatocyte growth factor mimetic, BB3.

What drug class is ANG-3777 in?

ANG-3777 belongs to the HGF mimetic class. See all HGF mimetic drugs at /class/hgf-mimetic.

What development phase is ANG-3777 in?

ANG-3777 is in Phase 3.

What does ANG-3777 target?

ANG-3777 targets MET receptor and is a HGF mimetic.

Related

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