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IASLC Announces FDA Accelerated Approval of Emrelis for Advanced NSCLC
May 16, 2025, 06:13

IASLC Announces FDA Accelerated Approval of Emrelis for Advanced NSCLC

International Association for the Study of Lung Cancer (IASLC) posted on LinkedIn:

FDA Accelerated Approval Alert

The FDA has granted accelerated approval to telisotuzumab vedotin-tllv (Emrelis) for adults with advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) showing high c-Met protein expression—after prior systemic treatment.

Based on the LUMINOSITY trial

• 35% overall response rate.
• Median duration of response: 7.2 months.

Why this matters for lung cancer care:

• Offers a new option for patients with high c-Met protein expression.
• Fills a treatment gap for previously treated NSCLC patients.
• Highlights the impact of biomarker-driven therapies.

Learn more.”

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