Gavreto (pralsetinib) vs Krazati (adagrasib)

Gavreto (pralsetinib) vs Krazati (adagrasib)

Gavreto (pralsetinib) and Krazati (adagrasib) are both targeted therapies used to treat certain types of non-small cell lung cancer (NSCLC) with specific genetic mutations. Gavreto is designed to inhibit RET fusion-positive NSCLC, and it is approved for patients with metastatic RET fusion-positive NSCLC. Krazati, on the other hand, targets KRAS G12C-mutated NSCLC and is indicated for adult patients with KRAS G12C-mutated locally advanced or metastatic NSCLC, as determined by an FDA-approved test, who have received at least one prior systemic therapy. The choice between these two medications would be guided by the specific genetic mutation present in the cancer, as determined by molecular testing.

Difference between Gavreto and Krazati

Metric Gavreto (pralsetinib) Krazati (adagrasib)
Generic name Pralsetinib Adagrasib
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 KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test, after at least one prior systemic therapy
Mechanism of action RET kinase inhibitor KRASG12C inhibitor
Brand names Gavreto Krazati
Administrative route Oral Oral
Side effects Includes hypertension, fatigue, constipation, musculoskeletal pain, and diarrhea Includes diarrhea, nausea, fatigue, musculoskeletal pain, and liver enzyme elevation
Contraindications Hypersensitivity to pralsetinib or any of its components Hypersensitivity to adagrasib or any of its components
Drug class Tyrosine kinase inhibitor Small molecule kinase inhibitor
Manufacturer Genentech, Inc. Mirati Therapeutics, Inc.

Efficacy

Gavreto (pralsetinib) Efficacy in Lung Cancer

Gavreto (pralsetinib) is a targeted therapy approved by the U.S. Food and Drug Administration (FDA) for the treatment of adults with metastatic non-small cell lung cancer (NSCLC) with rearrangements in the RET gene (RET fusion-positive). The efficacy of Gavreto was demonstrated in a clinical trial that included patients with RET fusion-positive NSCLC who were previously untreated or had received prior treatment. The trial showed a significant response rate, with a majority of patients experiencing tumor shrinkage. This response was also found to be durable, with many patients maintaining their response for six months or longer.

In patients who were treatment-naive, the response to Gavreto was particularly notable. The objective response rate (ORR) was high, indicating that the drug effectively inhibited tumor growth in a substantial proportion of patients. Additionally, Gavreto has shown a favorable safety profile, making it a viable option for patients with this specific genetic alteration in their lung cancer.

Krazati (adagrasib) Efficacy in Lung Cancer

Krazati (adagrasib) is another novel medication that targets a specific mutation in lung cancer. It is designed to inhibit the KRAS G12C mutation, which is a driver of cancer growth in a subset of patients with NSCLC. While Krazati is still under clinical investigation, early trial results have shown promise in patients with advanced NSCLC harboring the KRAS G12C mutation. The drug has demonstrated an ability to achieve tumor shrinkage in a significant number of patients, with some experiencing a partial or complete response to the treatment.

The clinical trials assessing the efficacy of Krazati in lung cancer are ongoing, and more data is expected to further define its role in the treatment landscape. However, the preliminary results suggest that Krazati could offer a new therapeutic option for patients with NSCLC who have the KRAS G12C mutation, a group for whom targeted therapies were previously unavailable. As research continues, Krazati may become an important addition to the arsenal of treatments for lung cancer, particularly for those with this specific genetic profile.

Regulatory Agency Approvals

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

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If Gavreto or Krazati 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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