Cyramza (ramucirumab) vs Braftovi (encorafenib)

Cyramza (ramucirumab) vs Braftovi (encorafenib)

Cyramza (ramucirumab) is a monoclonal antibody that targets the VEGF receptor 2 and is primarily used for the treatment of certain types of gastric or gastroesophageal junction adenocarcinoma, metastatic non-small cell lung cancer, and metastatic colorectal cancer. Braftovi (encorafenib) is a small molecule BRAF inhibitor indicated for the treatment of patients with BRAF V600E-mutant metastatic melanoma, as well as metastatic colorectal cancer with the same mutation, often in combination with other medications. The choice between Cyramza and Braftovi would depend on the specific type and genetic profile of the cancer; therefore, a healthcare provider would recommend a treatment based on the tumor's characteristics, the patient's overall health, and the treatment goal.

Difference between Cyramza and Braftovi

Metric Cyramza (ramucirumab) Braftovi (encorafenib)
Generic name ramucirumab encorafenib
Indications gastric cancer, colorectal cancer, non-small cell lung cancer, hepatocellular carcinoma unresectable or metastatic melanoma with a BRAF V600E or V600K mutation
Mechanism of action vascular endothelial growth factor receptor 2 antagonist BRAF kinase inhibitor
Brand names Cyramza Braftovi
Administrative route intravenous infusion oral
Side effects hypertension, diarrhea, headache, hyponatremia fatigue, nausea, vomiting, abdominal pain, arthralgia
Contraindications hypersensitivity to ramucirumab or any component of the formulation none known
Drug class monoclonal antibody, antineoplastic agent antineoplastic agent, BRAF inhibitor
Manufacturer Eli Lilly and Company Pfizer Inc. (in collaboration with Pierre Fabre)

Efficacy

Cyramza (Ramucirumab) Efficacy in Colorectal Cancer

Cyramza, known generically as ramucirumab, is a monoclonal antibody that targets the vascular endothelial growth factor receptor 2 (VEGFR2), which is implicated in the growth and development of blood vessels that supply tumors, a process known as angiogenesis. In the context of metastatic colorectal cancer, Cyramza has been evaluated for its efficacy in combination with other chemotherapy agents. Clinical trials have demonstrated that when used in combination with FOLFIRI (leucovorin, fluorouracil, and irinotecan), Cyramza has shown an improvement in overall survival and progression-free survival in patients with metastatic colorectal cancer who have progressed on a prior therapy containing bevacizumab, oxaliplatin, and a fluoropyrimidine.

Braftovi (Encorafenib) Efficacy in Colorectal Cancer

Braftovi, also known as encorafenib, is a kinase inhibitor specifically designed to target the BRAF V600E mutation, which is present in a subset of colorectal cancer cases. Encorafenib has been studied for its efficacy in metastatic colorectal cancer with the BRAF V600E mutation. In clinical trials, Braftovi, when used in combination with cetuximab (an epidermal growth factor receptor inhibitor), has shown a significant improvement in overall survival and progression-free survival compared to standard therapies. This combination is particularly notable because BRAF-mutant colorectal cancers are often more aggressive and historically have had fewer effective treatment options.

Combination Therapy in Colorectal Cancer

The use of combination therapies, such as Cyramza with FOLFIRI and Braftovi with cetuximab, represents a strategic approach to target different pathways involved in colorectal cancer progression. These combinations have been shown to improve outcomes in patients with specific characteristics, such as those with metastatic disease and certain genetic mutations. The choice of therapy is heavily dependent on the molecular profile of the tumor and the patient's prior treatment history.

Conclusion

In conclusion, both Cyramza and Braftovi have demonstrated efficacy in the treatment of metastatic colorectal cancer in their respective contexts. Cyramza, in combination with FOLFIRI, offers an option for patients who have failed previous therapies, while Braftovi, in combination with cetuximab, provides a targeted approach for those with the BRAF V600E mutation. The success of these treatments underscores the importance of personalized medicine and the need for precise genetic profiling in the management of colorectal cancer.

Regulatory Agency Approvals

Cyramza
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Braftovi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Cyramza or Braftovi today

If Cyramza or Braftovi are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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