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Ramucirumab

Monoclonal Antibody · Antineoplastic

Monoclonal AntibodyAntineoplastic
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
not curated
Top interactionssee all 12
  • AbciximabSevereDatabaseDDInter
  • AcalabrutinibSevereDatabaseDDInter
  • AlteplaseSevereDatabaseDDInter
  • AnagrelideSevereDatabaseDDInter

Mechanism

Ramucirumab is a human IgG1 monoclonal antibody that selectively binds to the vascular endothelial growth factor receptor-2 (VEGFR-2). This binding prevents the attachment of VEGF-A, VEGF-C, and VEGF-D ligands to VEGFR-2, thereby inhibiting VEGF-induced angiogenesis. It also inhibits tumor vascular permeability and enhances tumor blood flow and drug delivery.

Indications

Treatment of advanced gastric cancer or gastro-oesophageal junction adenocarcinoma, in combination with paclitaxel, in patients with disease progression after prior platinum and fluoropyrimidine chemotherapy.Treatment of advanced gastric cancer or gastro-oesophageal junction adenocarcinoma, as monotherapy, in patients with disease progression after prior platinum or fluoropyrimidine chemotherapy, and for whom treatment in combination with paclitaxel is not appropriate.Treatment of metastatic colorectal cancer, in combination with FOLFIRI (irinotecan, fluorouracil and folinic acid), in patients with disease progression on, or after, prior therapy with bevacizumab, oxaliplatin and a fluoropyrimidine.Treatment of non-small cell lung cancer.metastatic colorectal cancer (mCRC) with disease progression on or after prior therapyadvanced gastric adenocarcinoma (single agent or in combination with paclitaxel) with disease progression on or after prior chemotherapymetastatic NSCLC (in combination with docetaxel) with disease progression on or after chemotherapy

Dosing

Adult
BY INTRAVENOUS INFUSION: For advanced gastric cancer or gastro-oesophageal junction adenocarcinoma, in combination with paclitaxel: 8 mg/kg on days 1 and 15 of a 28-day cycle, administered prior to paclitaxel infusion. For advanced gastric cancer or gastro-oesophageal junction adenocarcinoma, as monotherapy: 8 mg/kg every 2 weeks.…

Pharmacokinetics

Half-life
14 days (mean)

Side effects

Common
Hypertensiondiarrhea
Serious
  • Arterial thromboembolic events
  • gastrointestinal perforation
  • wound healing complications
  • bleeding complications
  • diarrhea
  • mucositis
  • proteinuria
  • increased risk of hemorrhage
  • impaired wound healing

Drug interactions

Abciximab
Severe
Database

Clinical effect not specified

Source: DDInter

Acalabrutinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Alteplase
Severe
Database

Clinical effect not specified

Source: DDInter

Anagrelide
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anisindione
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anistreplase
Severe
Database

Clinical effect not specified

Source: DDInter

Antithrombin Alfa
Severe
Database

Clinical effect not specified

Source: DDInter

Antithrombin Iii Human
Severe
Database

Clinical effect not specified

Source: DDInter

Apixaban
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Ardeparin
Severe
Database

Clinical effect not specified

Source: DDInter

Argatroban
Severe
Database

Clinical effect not specified

Source: DDInter

Aspirin
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Related guidelines

Other Monoclonal Antibody drugs

Ask House about Ramucirumab

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Sources: Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-13 · House clinical team