Last reviewed · How we verify

Bevacizumab-Pfizer

Pfizer · Phase 3 active Small molecule

Bevacizumab-Pfizer is a VEGF inhibitor (monoclonal antibody) Small molecule drug developed by Pfizer. It is currently in Phase 3 development for Metastatic colorectal cancer, Metastatic non-small cell lung cancer, Metastatic breast cancer.

Bevacizumab is a monoclonal antibody that blocks vascular endothelial growth factor (VEGF), preventing tumor blood vessel formation and starving tumors of oxygen and nutrients.

Bevacizumab is a monoclonal antibody that blocks vascular endothelial growth factor (VEGF), preventing tumor blood vessel formation and starving tumors of oxygen and nutrients. Used for Metastatic colorectal cancer, Metastatic non-small cell lung cancer, Metastatic breast cancer.

Likelihood of approval
64.3% 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).
  • Oncology Phase 3 boost +3.0pp
    Oncology Phase 3 trials have higher approval rates (~61%) than the cross-industry average due to clearer endpoints and FDA oncology pathway.
  • Big-pharma sponsor +3.0pp
    Pfizer is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
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 nameBevacizumab-Pfizer
SponsorPfizer
Drug classVEGF inhibitor (monoclonal antibody)
TargetVEGF (Vascular Endothelial Growth Factor)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Bevacizumab binds to circulating VEGF, a key signaling protein that promotes angiogenesis (new blood vessel growth). By neutralizing VEGF, the drug inhibits the formation of new blood vessels that tumors require to grow and metastasize. This anti-angiogenic mechanism reduces tumor perfusion and can slow or halt tumor progression.

Approved indications

Common side effects

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 Bevacizumab-Pfizer

What is Bevacizumab-Pfizer?

Bevacizumab-Pfizer is a VEGF inhibitor (monoclonal antibody) drug developed by Pfizer, indicated for Metastatic colorectal cancer, Metastatic non-small cell lung cancer, Metastatic breast cancer.

How does Bevacizumab-Pfizer work?

Bevacizumab is a monoclonal antibody that blocks vascular endothelial growth factor (VEGF), preventing tumor blood vessel formation and starving tumors of oxygen and nutrients.

What is Bevacizumab-Pfizer used for?

Bevacizumab-Pfizer is indicated for Metastatic colorectal cancer, Metastatic non-small cell lung cancer, Metastatic breast cancer, Recurrent glioblastoma, Metastatic renal cell carcinoma.

Who makes Bevacizumab-Pfizer?

Bevacizumab-Pfizer is developed by Pfizer (see full Pfizer pipeline at /company/pfizer).

What drug class is Bevacizumab-Pfizer in?

Bevacizumab-Pfizer belongs to the VEGF inhibitor (monoclonal antibody) class. See all VEGF inhibitor (monoclonal antibody) drugs at /class/vegf-inhibitor-monoclonal-antibody.

What development phase is Bevacizumab-Pfizer in?

Bevacizumab-Pfizer is in Phase 3.

What are the side effects of Bevacizumab-Pfizer?

Common side effects of Bevacizumab-Pfizer include Hypertension, Proteinuria, Hemorrhage (any grade), Thrombotic events, Gastrointestinal perforation, Wound healing complications.

What does Bevacizumab-Pfizer target?

Bevacizumab-Pfizer targets VEGF (Vascular Endothelial Growth Factor) and is a VEGF inhibitor (monoclonal antibody).

Related

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