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Proven clinical trial results

In a clinical trial, TABRECTA was studied in different groups of people with MET exon 14 skipping: those taking TABRECTA as their first treatment and those previously treated before taking TABRECTA.

  • The overall response rate measures the size or number of tumors people have. This includes:

    • people whose tumors became smaller or fewer in number (which is called a partial response), and

    • people whose tumors disappeared completely (which is called a complete response). A complete response is not the same thing as a cure.

  • Duration of response is the length of time that a tumor continues to respond to treatment without the cancer growing or spreading.

For people taking TABRECTA as their first treatment. Overall response rate: nearly 7 in 10 (68%) people had their tumors shrink or disappear.

For people taking it as their first treatment, TABRECTA is proven to shrink tumors. Among those previously untreated, 68% of 60 people achieved a response with TABRECTA. Of these responders, 5% had a complete response and 63% had a partial response.

Duration of response. Response lasted more than 1 year (16.6 months).

The median (or midpoint) duration of response for people taking TABRECTA as their first treatment was 16.6 months. This means that half of the people who responded to treatment continued to respond for longer than 16.6 months and half responded for less than 16.6 months. 

For people taking TABRECTA after taking another medicine. Overall response rate: More than 4 in 10 people had their tumors shrink or disappear.

For people who were previously treated, TABRECTA is proven to shrink tumors. Among those previously treated, 44% of 100 people achieved a response with TABRECTA. Of these responders, 0 people had a complete response and 44% had a partial response. 

Duration of response: 9.7 months.

The median (or midpoint) duration of response for people who were previously treated before taking TABRECTA was 9.7 months. This means that half of the people who responded to treatment continued to respond for longer than 9.7 months and half responded for less than 9.7 months. 

Important Safety Information

TABRECTA may cause serious side effects. Tell your health care provider right away if you get any of the following:

  • Lung or breathing problems. TABRECTA may cause inflammation of the lungs that can cause death. Tell your health care provider right away if...

Approved Use

TABRECTA is a prescription medicine used to treat adults with a kind of lung cancer called non-small cell lung cancer (NSCLC) that:

  • has spread to other parts of the body (metastatic), and 
  • whose tumors have an abnormal mesenchymal ...
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