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  • PBAC results on Leclaza that was listed in 165 days show...
  • by Lee, Hye-Kyung | translator Kang, Shin-Kook | Aug 6, 2021 06:05am
Used the approval-benefit appraisal linkage system¡¦ the nation¡¯s 31st novel drug to be listed at an unprecedented speed
Academic societies ¡°fully expect Leclaza to become an alternative for Tagrisso¡±
¡®Leclaza tab. (lazertinib mesylate monohydrate),' the 31st novel drug to be developed in Korea that received approval for insurance benefit in only 165 days after its approval, was reviewed as a 'new treatment alternative for non-small cell lung cancer patients' in the evaluation process for assessing the reasonableness of the medical care benefits for drugs.

The Health Insurance Review and Assessment Service (HIRA) had recently disclosed the results and minutes of the benefit evaluation that was conducted on Leclaza by the Pharmaceutical Benefit Assessment Committee on April 8th.


Leclaza was approved by the Ministry of Food and Drug Safety on January 18th as a ¡®treatment for patients with EGFR T790M mutati
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