Gavreto (pralsetinib) vs Exkivity (mobocertinib)

Gavreto (pralsetinib) vs Exkivity (mobocertinib)

Gavreto (pralsetinib) and Exkivity (mobocertinib) are both targeted therapies for non-small cell lung cancer (NSCLC) with specific genetic mutations. Gavreto is designed to treat NSCLC with RET gene alterations, while Exkivity is used for NSCLC with EGFR exon 20 insertion mutations. A patient's eligibility for either medication would depend on the presence of these specific mutations in their cancer cells, which can be determined through molecular testing recommended by their oncologist.

Difference between Gavreto and Exkivity

Metric Gavreto (pralsetinib) Exkivity (mobocertinib)
Generic name Pralsetinib Mobocertinib
Indications For the treatment of adult patients with metastatic RET fusion-positive non-small cell lung cancer (NSCLC) For the treatment of adult patients with locally advanced or metastatic NSCLC with epidermal growth factor receptor (EGFR) exon 20 insertion mutations
Mechanism of action RET kinase inhibitor EGFR kinase inhibitor
Brand names Gavreto Exkivity
Administrative route Oral Oral
Side effects Includes hypertension, fatigue, constipation, and rash Includes diarrhea, rash, nausea, and vomiting
Contraindications Hypersensitivity to pralsetinib or any of the excipients Hypersensitivity to mobocertinib or any of the excipients
Drug class Antineoplastic agent Antineoplastic agent
Manufacturer Blueprint Medicines Corporation Takeda Pharmaceutical Company

Efficacy

Gavreto (pralsetinib) Efficacy in Lung Cancer

Gavreto (pralsetinib) is a targeted therapy approved for the treatment of adults with metastatic non-small cell lung cancer (NSCLC) with RET (rearranged during transfection) gene fusions. RET gene fusions are a rare driver in NSCLC, and Gavreto is designed to inhibit the kinase activity of the RET fusion proteins. Clinical trials have demonstrated that pralsetinib is effective in inducing responses in patients with RET fusion-positive NSCLC. The efficacy was shown in a multicenter, open-label, multi-cohort clinical study where patients treated with Gavreto experienced a significant overall response rate (ORR), indicating a reduction in tumor size. The duration of response (DOR) also supported the efficacy of this medication, with many patients showing sustained responses.

Exkivity (mobocertinib) Efficacy in Lung Cancer

Exkivity (mobocertinib) is an oral medication approved for the treatment of adult patients with metastatic NSCLC harboring epidermal growth factor receptor (EGFR) exon 20 insertion mutations, whose disease has progressed on or after platinum-based chemotherapy. This subset of NSCLC is challenging to treat due to the lack of effective therapies targeting the EGFR exon 20 insertions. Exkivity has shown efficacy in clinical trials, where it demonstrated an ORR, indicating that the treatment could shrink or control the cancer in a significant number of patients. The DOR with Exkivity was also noteworthy, providing evidence of its sustained antitumor activity in this patient population.

Comparison of Efficacy in Lung Cancer

Both Gavreto and Exkivity are examples of precision medicine, targeting specific mutations in lung cancer cells. While they target different mutations, their development represents a shift towards personalized treatment in lung cancer care. The efficacy of both drugs is specific to the mutations they target, and they have provided new treatment options for patients with these specific genetic alterations. The clinical benefits of Gavreto and Exkivity have been substantial for patients with few other treatment options, offering hope for improved outcomes.

Conclusion

The introduction of targeted therapies such as Gavreto and Exkivity has significantly impacted the treatment landscape of NSCLC. Their efficacy in treating specific genetic alterations in lung cancer highlights the importance of molecular testing in the management of this disease. As research continues, these medications may offer further insights into personalized cancer care and potentially improve the prognosis for patients with lung cancer harboring these genetic changes.

Regulatory Agency Approvals

Gavreto
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Exkivity
  • Food and Drug Administration (FDA), USA

Access Gavreto or Exkivity today

If Gavreto or Exkivity 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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