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Tepotinib is approved by the USFDA for metastatic non-small cell lung cancer

Susan HauWritten by Susan HauMedically ReviewedUpdated March 5, 20244 min read
Tepotinib is approved by the USFDA for metastatic non-small cell lung cancer
In this article
  1. FDA Full Approval of Tepotinib for METex14 NSCLC
  2. VISION Clinical Trial and Patient Outcomes
  3. Common Adverse Effects and Patient Safety
  4. Recommended Dosage and Administration Guidelines
  5. How CancerFax Helps

FDA Full Approval of Tepotinib for METex14 NSCLC

The Food and Drug Administration officially approved tepotinib (Tepmetko, EMD Serono, Inc.) on February 15, 2024, for adult patients with metastatic non-small cell lung cancer (NSCLC) that had mesenchymal-epithelial transition (MET) exon 14 skipping mutations.

Tepotinib received accelerated clearance for this use on February 3, 2021, after showing positive results in the VISION trial (NCT02864992), which was a multicenter, non-randomized, open-label, multicohort research. The transition to conventional approval was made after including 161 more patients and extending the follow-up period by 28 months to evaluate the duration of response.

VISION Clinical Trial and Patient Outcomes

Effectiveness was proven in 313 individuals with metastatic non-small cell lung cancer (NSCLC) carrying MET exon skipping mutations. Patients were administered a daily dose of 450 mg of tepotinib until disease progression or unacceptable toxicity occurred.

The main effectiveness criteria were Objective Response Rate (ORR) and Duration of Response (DOR), assessed by a Blinded Independent Review Committee. Out of 164 patients who had not had treatment before, the Objective Response Rate (ORR) was 57% with a 95% Confidence Interval (CI) of 49 to 65. Among the responders, 40% had a Duration of Response (DOR) of 12 months or more. Out of 149 patients who had received treatment before, the Objective Response Rate (ORR) was 45% with a 95% Confidence Interval (CI) of 37 to 53. Additionally, 36% of the responders had a Duration of Response (DOR) of 12 months or more.

Common Adverse Effects and Patient Safety

The predominant adverse effects (≥20%) included edema, nausea, exhaustion, musculoskeletal pain, diarrhea, dyspnea, decreased appetite, and rash.

Recommended Dosage and Administration Guidelines

The suggested dose of tepotinib is 450 mg taken orally once a day with meals.

View full prescribing information for Tepmetko.

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Susan Hau

About Susan Hau

Susan Hau is a distinguished researcher in the field of cancer cell therapy, with a particular focus on T cell-based approaches and cancer vaccines. Her work spans several innovative treatment modalities, including CAR T-cell therapy, TIL (Tumor-Infiltrating Lymphocyte) therapy, and NK (Natural Killer) cell therapy. Hau's expertise lies in cancer cell biolo…

✓ Reviewed for medical accuracy by the CancerFax review panel.

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