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U S Food and Drug Administration Approves Augtyro™ (repotrectinib), a Next-Generation Tyrosine Kinase Inhibitor (TKI), for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors

U S Food and Drug Administration Approves Augtyro™ (repotrectinib), a Next-Generation Tyrosine Kinase Inhibitor (TKI), for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors
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U S Food and Drug Administration Approves Augtyrotm (repotrectinib), a Next-Generation Tyrosine Kinase Inhibitor (TKI), for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors

Bristol Myers Squibb today announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval of Augtyrotm (repotrectinib) for the treatment of adult and pediatric patients 12 years of age and older with solid tumors that.

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Bristol Myers Squibb Wins FDA Approval for Lung Cancer Drug From $4B Deal

FDA approval of Bristol Myers Squibb’s Augtyro covers treatment of patients whose non-small cell lung cancer is driven by the rare ROS1 mutation. The molecule comes from BMS’s 2022 acquisition of Turning Point Therapeutics.

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Bristol Myers CAR-T therapy cleared by FDA for earlier lymphoma use

BioPharma

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Bristol Myers keeps the perioperative ball rolling with Opdivo nod in postsurgery bladder cancer

Bristol Myers keeps the perioperative ball rolling with Opdivo nod in postsurgery bladder cancer
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New yorkUnited statesNick botwoodBristol myersMerck coBristol myers squibbNektar therapeuticபுதியது யார்க்ஒன்றுபட்டது மாநிலங்களில்நிக் போட்வுட்பிரிஸ்டல் மைஸ்மெர்க் இணைபிரிஸ்டல் மைஸ் ஸ்க்விப்ப்னெக்தார் சிகிச்சை