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  • Pfizer seeks for approval on NSCLC drug ¡®lorlatinib¡¯
  • by Kim, Jin-Gu | translator Byun Kyung A | Oct 12, 2020 06:15am
As Xalkori latecomer ALK inhibitor, patients tolerant with other options have high expectation
Drug with the most number of treatment purpose use approval in 2020 with 134 out of 326 cases
 ¡ã A product image of Pfizer¡¯s ALK-positive NSCLC treatment lorlatinib (brand name Lorbrena)
Pfizer has taken a first step to launch a non-small cell lung cancer (NSCLC) treatment ¡®lorlatinib¡¯ in the South Korean market.

According to a pharmaceutical industry source on Oct. 7, Pfizer Pharmaceutical Korea has recently submitted an application to the Ministry of Food and Drug Safety (MFDS) to request an item approval on lorlatinib. After getting designated as an orphan drug in March by MFDS, the company initiated the approval application preparation in South Korea. In November last year, the product has been approved in the U.S. under the brand name Lorbrena.

Lorlatinib is a latecomer to Pfizer¡¯s anaplastic lymphoma kinase (ALK)-positive NSCLC treatment Xalkori (crizotinib).

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