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    The next Met Gala exhibit will spotlight fashion across art history – San Francisco Chronicle

    The next Met Gala exhibit will spotlight fashion across art history – San Francisco Chronicle

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    The next Met Gala exhibit will spotlight fashion across art history – San Francisco Chronicle

    The next Met Gala exhibit will spotlight fashion across art history – San Francisco Chronicle

    The Running Man to David Hockney: your complete entertainment guide to the week ahead | Culture – The Guardian

    The Running Man to David Hockney: your complete entertainment guide to the week ahead | Culture – The Guardian

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    Kelly Brook opens up on ‘horrific’ miscarriage that left her never wanting to try for a baby again – Woman & Home

    Bartlett Police investigating shooting at kids entertainment center, officials say – FOX13 Memphis

    Shooting at Kids Entertainment Center Under Investigation by Bartlett Police

    We’re looking to further trim this drug stock and exit this entertainment giant – CNBC

    We’re looking to further trim this drug stock and exit this entertainment giant – CNBC

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    Cracking the Code: Why China’s Economic Challenges Aren’t Shaking Markets, Unlike America’s” – Bloomberg

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    Israel-Gaza war live updates: Hamas leader Ismail Haniyeh assassinated in Iran, group says

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    PAP Boss to Niger Delta Youths, Stay Away from the Protest

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    Continental Uses Vacuum Technology to Study Tire Wear Particles – Continental AG

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FDA Expands Repotrectinib Label

June 13, 2024
in Health
FDA Expands Repotrectinib Label
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The US Food and Drug Administration has granted accelerated approval to repotrectinib (Augtyro, Bristol Myers Squibb) for all locally advanced, unresectable, or metastatic solid tumors with an NTRK gene fusion that have progressed after initial treatment or that have no satisfactory alternative therapies.

The approval is a label expansion for the tyrosine kinase inhibitor (TKI), which received initial clearance in November 2023 for locally advanced or metastatic ROS1-positive non–small cell lung cancer. 

NTRK gene fusions are genetic abnormalities wherein part of the NTRK gene fuses with an unrelated gene. The abnormal gene can then produce an oncogenic protein. Although rare, these mutations are found in many cancer types.

The approval, for adult and pediatric patients aged 12 years or older, was based on the single-arm open-label TRIDENT-1 trial in 88 adults with locally advanced or metastatic NTRK gene fusion solid tumors.

In the 40 patients who were TKI-naive, the overall response rate was 58%, and the median duration of response was not estimable. In the 48 patients who had a TKI previously, the overall response rate was 50% and median duration of response was 9.9 months.

In 20% or more of participants, treatment caused dizziness, dysgeusia, peripheral neuropathy, constipation, dyspnea, fatigue, ataxia, cognitive impairment, muscular weakness, and nausea.

Labelling warns of central nervous system reactions, interstitial lung disease/pneumonitis, hepatotoxicity, myalgia with creatine phosphokinase elevation, hyperuricemia, bone fractures, and embryo-fetal toxicity.

The recommended dose is 160 mg orally once daily for 14 days then increased to 160 mg twice daily until disease progression or unacceptable toxicity.

Sixty 40-mg capsules cost around $7644, according to drugs.com. 

M. Alexander Otto is a physician assistant with a master’s degree in medical science and a journalism degree from Newhouse. He is an award-winning medical journalist who worked for several major news outlets before joining Medscape. Alex is also an MIT Knight Science Journalism fellow. Email: [email protected]

>>> Read full article>>>
Copyright for syndicated content belongs to the linked Source : Medscape – https://www.medscape.com/viewarticle/fda-expands-repotrectinib-label-all-ntrk-gene-fusion-solid-2024a1000b3q

Tags: expandshealthRepotrectinib
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