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Taletrectinib
Taletrectinib

Taletrectinib(己二酸他雷替尼胶囊)

Its core advantages are potent ROS1 inhibition, high intracranial activity, outstanding anti-resistance efficacy, superior safety profile, and high accessibility.

  • 200mg*33capsules

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Taletrectinib Drug News

On December 20, 2024, taletrectinib was approved by the National Medical
Products Administration (NMPA) of China for the treatment of adult patients with
ROS1‑positive locally advanced or metastatic non‑small cell lung cancer (NSCLC)
who have progressed following treatment with a ROS1 tyrosine kinase inhibitor
(TKI).

On January 2, 2025, an additional indication was approved for taletrectinib,
for the treatment of adult patients with ROS1‑positive locally advanced or
metastatic NSCLC who are treatment‑naïve to ROS1‑TKIs.

On January 1, 2026, taletrectinib was included in the 2025 edition of the
National Reimbursement Drug List (NRDL) of China.

On June 11, 2025, taletrectinib was approved in the United States for the
treatment of adult patients with locally advanced or metastatic ROS1‑positive
NSCLC, regardless of prior TKI treatment history.

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