Peringatan Keamanan

Ramucirumab packaging includes warnings for arterial thromboembolic events, hypertension, infusion-related reactions, gastrointestinal perforation, clinical deterioration in patients with cirrhosis, and reversible posterior leukoencephalopathy syndrome. The most common reactions observed in single-agent-treated patients at a rate of >10% and >2% higher than placebo were hypertension and diarrhea. The most common adverse reactions observed in patients treated with ramucirumab plus paclitaxel at a rate of of >30% and >2% higher than placebo plus paclitaxel were fatigue, neutropenia, diarrhea, and epistaxis.

Ramucirumab

DB05578

biotech approved investigational

Deskripsi

Ramucirumab is a human monoclonal antibody (IgG1) against vascular endothelial growth factor receptor 2 (VEGFR2), a type II trans-membrane tyrosine kinase receptor expressed on endothelial cells. By binding to VEGFR2, ramucirumab prevents binding of its ligands (VEGF-A, VEGF-C, and VEGF-D), thereby preventing VEGF-stimulated receptor phosphorylation and downstream ligand-induced proliferation, permeability, and migration of human endothelial cells. VEGFR stimulation also mediates downstream signalling required for angiogenesis and is postulated to be heavily involved in cancer progression, making it a highly likely drug target. In contrast to other agents directed against VEGFR-2, ramucirumab binds a specific epitope on the extracellular domain of VEGFR-2, thereby blocking all VEGF ligands from binding to it. Ramucirumab is indicated for us in advanced gastric or gastro-esophageal junction adenocarcinoma as a single agent or in combination with paclitaxel after prior fluoropyrimidine- or platinum-containing chemotherapy.

Struktur Molekul 2D

Struktur tidak tersedia

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) 15 days
Volume Distribusi 5.5 L
Klirens (Clearance) 0.014 L/hour

Absorpsi

Data absorpsi tidak tersedia.

Metabolisme

Data metabolisme tidak tersedia.

Rute Eliminasi

Data eliminasi belum tersedia.

Interaksi Obat

420 Data
Diethylstilbestrol Diethylstilbestrol may increase the thrombogenic activities of Ramucirumab.
Chlorotrianisene Chlorotrianisene may increase the thrombogenic activities of Ramucirumab.
Conjugated estrogens Conjugated estrogens may increase the thrombogenic activities of Ramucirumab.
Estrone Estrone may increase the thrombogenic activities of Ramucirumab.
Estradiol Estradiol may increase the thrombogenic activities of Ramucirumab.
Dienestrol Dienestrol may increase the thrombogenic activities of Ramucirumab.
Ethinylestradiol Ethinylestradiol may increase the thrombogenic activities of Ramucirumab.
Mestranol Mestranol may increase the thrombogenic activities of Ramucirumab.
Estriol Estriol may increase the thrombogenic activities of Ramucirumab.
Estrone sulfate Estrone sulfate may increase the thrombogenic activities of Ramucirumab.
Quinestrol Quinestrol may increase the thrombogenic activities of Ramucirumab.
Hexestrol Hexestrol may increase the thrombogenic activities of Ramucirumab.
Tibolone Tibolone may increase the thrombogenic activities of Ramucirumab.
Synthetic Conjugated Estrogens, A Synthetic Conjugated Estrogens, A may increase the thrombogenic activities of Ramucirumab.
Synthetic Conjugated Estrogens, B Synthetic Conjugated Estrogens, B may increase the thrombogenic activities of Ramucirumab.
Polyestradiol phosphate Polyestradiol phosphate may increase the thrombogenic activities of Ramucirumab.
Esterified estrogens Esterified estrogens may increase the thrombogenic activities of Ramucirumab.
Zeranol Zeranol may increase the thrombogenic activities of Ramucirumab.
Equol Equol may increase the thrombogenic activities of Ramucirumab.
Promestriene Promestriene may increase the thrombogenic activities of Ramucirumab.
Methallenestril Methallenestril may increase the thrombogenic activities of Ramucirumab.
Epimestrol Epimestrol may increase the thrombogenic activities of Ramucirumab.
Moxestrol Moxestrol may increase the thrombogenic activities of Ramucirumab.
Estradiol acetate Estradiol acetate may increase the thrombogenic activities of Ramucirumab.
Estradiol benzoate Estradiol benzoate may increase the thrombogenic activities of Ramucirumab.
Estradiol cypionate Estradiol cypionate may increase the thrombogenic activities of Ramucirumab.
Estradiol valerate Estradiol valerate may increase the thrombogenic activities of Ramucirumab.
Biochanin A Biochanin A may increase the thrombogenic activities of Ramucirumab.
Formononetin Formononetin may increase the thrombogenic activities of Ramucirumab.
Estetrol Estetrol may increase the thrombogenic activities of Ramucirumab.
Cetuximab The risk or severity of adverse effects can be increased when Cetuximab is combined with Ramucirumab.
Human immunoglobulin G The risk or severity of adverse effects can be increased when Human immunoglobulin G is combined with Ramucirumab.
Omalizumab The risk or severity of adverse effects can be increased when Omalizumab is combined with Ramucirumab.
Adalimumab The risk or severity of adverse effects can be increased when Adalimumab is combined with Ramucirumab.
Abciximab The risk or severity of adverse effects can be increased when Abciximab is combined with Ramucirumab.
Gemtuzumab ozogamicin The risk or severity of adverse effects can be increased when Gemtuzumab ozogamicin is combined with Ramucirumab.
Indium In-111 satumomab pendetide The risk or severity of adverse effects can be increased when Indium In-111 satumomab pendetide is combined with Ramucirumab.
Infliximab The risk or severity of adverse effects can be increased when Infliximab is combined with Ramucirumab.
Trastuzumab The risk or severity of adverse effects can be increased when Trastuzumab is combined with Ramucirumab.
Rituximab The risk or severity of adverse effects can be increased when Rituximab is combined with Ramucirumab.
Basiliximab The risk or severity of adverse effects can be increased when Basiliximab is combined with Ramucirumab.
Muromonab The risk or severity of adverse effects can be increased when Muromonab is combined with Ramucirumab.
Digoxin Immune Fab (Ovine) The risk or severity of adverse effects can be increased when Digoxin Immune Fab (Ovine) is combined with Ramucirumab.
Ibritumomab tiuxetan The risk or severity of adverse effects can be increased when Ibritumomab tiuxetan is combined with Ramucirumab.
Tositumomab The risk or severity of adverse effects can be increased when Tositumomab is combined with Ramucirumab.
Alemtuzumab The risk or severity of adverse effects can be increased when Alemtuzumab is combined with Ramucirumab.
Capromab pendetide The risk or severity of adverse effects can be increased when Capromab pendetide is combined with Ramucirumab.
Efalizumab The risk or severity of adverse effects can be increased when Efalizumab is combined with Ramucirumab.
Antithymocyte immunoglobulin (rabbit) The risk or severity of adverse effects can be increased when Antithymocyte immunoglobulin (rabbit) is combined with Ramucirumab.
Natalizumab The risk or severity of adverse effects can be increased when Natalizumab is combined with Ramucirumab.
Palivizumab The risk or severity of adverse effects can be increased when Palivizumab is combined with Ramucirumab.
Daclizumab The risk or severity of adverse effects can be increased when Daclizumab is combined with Ramucirumab.
Bevacizumab The risk or severity of adverse effects can be increased when Bevacizumab is combined with Ramucirumab.
Technetium Tc-99m arcitumomab The risk or severity of adverse effects can be increased when Technetium Tc-99m arcitumomab is combined with Ramucirumab.
Eculizumab The risk or severity of adverse effects can be increased when Eculizumab is combined with Ramucirumab.
Panitumumab The risk or severity of adverse effects can be increased when Panitumumab is combined with Ramucirumab.
Ranibizumab The risk or severity of adverse effects can be increased when Ranibizumab is combined with Ramucirumab.
Galiximab The risk or severity of adverse effects can be increased when Galiximab is combined with Ramucirumab.
Pexelizumab The risk or severity of adverse effects can be increased when Pexelizumab is combined with Ramucirumab.
Afelimomab The risk or severity of adverse effects can be increased when Afelimomab is combined with Ramucirumab.
Epratuzumab The risk or severity of adverse effects can be increased when Epratuzumab is combined with Ramucirumab.
Bectumomab The risk or severity of adverse effects can be increased when Bectumomab is combined with Ramucirumab.
Oregovomab The risk or severity of adverse effects can be increased when Oregovomab is combined with Ramucirumab.
IGN311 The risk or severity of adverse effects can be increased when IGN311 is combined with Ramucirumab.
Adecatumumab The risk or severity of adverse effects can be increased when Adecatumumab is combined with Ramucirumab.
Labetuzumab The risk or severity of adverse effects can be increased when Labetuzumab is combined with Ramucirumab.
Matuzumab The risk or severity of adverse effects can be increased when Matuzumab is combined with Ramucirumab.
Fontolizumab The risk or severity of adverse effects can be increased when Fontolizumab is combined with Ramucirumab.
Bavituximab The risk or severity of adverse effects can be increased when Bavituximab is combined with Ramucirumab.
CR002 The risk or severity of adverse effects can be increased when CR002 is combined with Ramucirumab.
Rozrolimupab The risk or severity of adverse effects can be increased when Rozrolimupab is combined with Ramucirumab.
Girentuximab The risk or severity of adverse effects can be increased when Girentuximab is combined with Ramucirumab.
Obiltoxaximab The risk or severity of adverse effects can be increased when Obiltoxaximab is combined with Ramucirumab.
XTL-001 The risk or severity of adverse effects can be increased when XTL-001 is combined with Ramucirumab.
NAV 1800 The risk or severity of adverse effects can be increased when NAV 1800 is combined with Ramucirumab.
Briakinumab The risk or severity of adverse effects can be increased when Briakinumab is combined with Ramucirumab.
Otelixizumab The risk or severity of adverse effects can be increased when Otelixizumab is combined with Ramucirumab.
AMG 108 The risk or severity of adverse effects can be increased when AMG 108 is combined with Ramucirumab.
Iratumumab The risk or severity of adverse effects can be increased when Iratumumab is combined with Ramucirumab.
Enokizumab The risk or severity of adverse effects can be increased when Enokizumab is combined with Ramucirumab.
Farletuzumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Farletuzumab.
Veltuzumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Veltuzumab.
Ustekinumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Ustekinumab.
Trastuzumab emtansine The risk or severity of adverse effects can be increased when Ramucirumab is combined with Trastuzumab emtansine.
PRO-542 The risk or severity of adverse effects can be increased when Ramucirumab is combined with PRO-542.
TNX-901 The risk or severity of adverse effects can be increased when Ramucirumab is combined with TNX-901.
Inotuzumab ozogamicin The risk or severity of adverse effects can be increased when Ramucirumab is combined with Inotuzumab ozogamicin.
RI 624 The risk or severity of adverse effects can be increased when Ramucirumab is combined with RI 624.
Stamulumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with MYO-029.
CT-011 The risk or severity of adverse effects can be increased when Ramucirumab is combined with CT-011.
Leronlimab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Leronlimab.
Glembatumumab vedotin The risk or severity of adverse effects can be increased when Ramucirumab is combined with Glembatumumab vedotin.
Olaratumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Olaratumab.
IPH 2101 The risk or severity of adverse effects can be increased when Ramucirumab is combined with IPH 2101.
TB-402 The risk or severity of adverse effects can be increased when Ramucirumab is combined with TB-402.
Caplacizumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Caplacizumab.
IMC-1C11 The risk or severity of adverse effects can be increased when Ramucirumab is combined with IMC-1C11.
Eldelumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Eldelumab.
Lumiliximab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Lumiliximab.
Canakinumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with Canakinumab.

Target Protein

Vascular endothelial growth factor receptor 2 KDR

Referensi & Sumber

Synthesis reference: http://www.ema.europa.eu/docs/enGB/documentlibrary/EPAR-Publicassessmentreport/human/002829/WC500180726.pdf
Artikel (PubMed)
  • PMID: 26048277
    Casak SJ, Fashoyin-Aje I, Lemery SJ, Zhang L, Jin R, Li H, Zhao L, Zhao H, Zhang H, Chen H, He K, Dougherty M, Novak R, Kennett S, Khasar S, Helms W, Keegan P, Pazdur R: FDA Approval Summary: Ramucirumab for Gastric Cancer. Clin Cancer Res. 2015 Aug 1;21(15):3372-6. doi: 10.1158/1078-0432.CCR-15-0600. Epub 2015 Jun 5.
  • PMID: 25378934
    Aprile G, Rijavec E, Fontanella C, Rihawi K, Grossi F: Ramucirumab: preclinical research and clinical development. Onco Targets Ther. 2014 Oct 29;7:1997-2006. doi: 10.2147/OTT.S61132. eCollection 2014.
  • PMID: 25281695
    Javle M, Smyth EC, Chau I: Ramucirumab: successfully targeting angiogenesis in gastric cancer. Clin Cancer Res. 2014 Dec 1;20(23):5875-81. doi: 10.1158/1078-0432.CCR-14-1071. Epub 2014 Oct 3.
  • PMID: 24277700
    Aprile G, Bonotto M, Ongaro E, Pozzo C, Giuliani F: Critical appraisal of ramucirumab (IMC-1121B) for cancer treatment: from benchside to clinical use. Drugs. 2013 Dec;73(18):2003-15. doi: 10.1007/s40265-013-0154-8.
  • PMID: 2182794
    Goodkin R, Zaias B, Michelsen WJ: Arteriovenous malformation and glioma: coexistent or sequential? Case report. J Neurosurg. 1990 May;72(5):798-805.
  • PMID: 19636328
    Grothey A, Galanis E: Targeting angiogenesis: progress with anti-VEGF treatment with large molecules. Nat Rev Clin Oncol. 2009 Sep;6(9):507-18. doi: 10.1038/nrclinonc.2009.110. Epub 2009 Jul 28.
  • PMID: 20048182
    Spratlin JL, Cohen RB, Eadens M, Gore L, Camidge DR, Diab S, Leong S, O'Bryant C, Chow LQ, Serkova NJ, Meropol NJ, Lewis NL, Chiorean EG, Fox F, Youssoufian H, Rowinsky EK, Eckhardt SG: Phase I pharmacologic and biologic study of ramucirumab (IMC-1121B), a fully human immunoglobulin G1 monoclonal antibody targeting the vascular endothelial growth factor receptor-2. J Clin Oncol. 2010 Feb 10;28(5):780-7. doi: 10.1200/JCO.2009.23.7537. Epub 2010 Jan 4.
  • PMID: 11774295
    Lu D, Jimenez X, Zhang H, Bohlen P, Witte L, Zhu Z: Selection of high affinity human neutralizing antibodies to VEGFR2 from a large antibody phage display library for antiangiogenesis therapy. Int J Cancer. 2002 Jan 20;97(3):393-9.

Contoh Produk & Brand

Produk: 6 • International brands: 0
Produk
  • Cyramza
    Injection, solution, concentrate • 10 mg/ml • Intravenous • EU • Approved
  • Cyramza
    Injection, solution, concentrate • 10 mg/ml • Intravenous • EU • Approved
  • Cyramza
    Injection, solution, concentrate • 10 mg/ml • Intravenous • EU • Approved
  • Cyramza
    Solution • 10 mg/1mL • Intravenous • US • Approved
  • Cyramza
    Solution • 10 mg/1mL • Intravenous • US • Approved
  • Cyramza
    Solution • 10 mg / mL • Intravenous • Canada • Approved

Sekuens Gen/Protein (FASTA)

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