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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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Susan spinosaAlexander drilonNick botwoodBristol myers squibbNational cancer instituteDrug administrationExchange commissionBristol myers squibb companyEuropean society for medical oncologyEarly drug development serviceMemorial sloan kettering cancerImportant safety informationMedical oncologyBristol myersBlinded independent central reviewResponse evaluation criteria

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.

Bristol myers squibbNick botwoodAlexander drilonSusan spinosaDrug administration approves augtyrotmNational cancer instituteBristol myers squibb companyExchange commissionProduct serviceEuropean society for medical oncologyDrug administrationNext generation tyrosine kinase inhibitorPositive locally advancedMetastatic solidMyers squibbEarly drug development service

Dostarlimab With Carboplatin/Paclitaxel Shows Survival Benefits in dMMR/MSI-H Endometrial Cancer

Dostarlimab plus carboplatin and paclitaxel improved PFS and OS in dMMR/MSI-H primary advanced or recurrent endometrial cancer.

Response evaluation criteriaSolid tumors

Merus Presents Interim Data on MCLA-145 Monotherapy and in Combination with Pembrolizumab at the 2024 ASCO® Annual Meeting

UTRECHT, The Netherlands and CAMBRIDGE, Mass., June 02, 2024 Merus N.V. , a clinical-stage oncology company developing innovative, full-length multispecific antibodies , today announced updated.

United kingdomUnited statesChicago mayAmerican society of clinical oncologyExchange commissionAnnual meetingBill lundbergChief executive officerSolid tumorsResponse evaluation criteriaPrivate securities litigation reform actAnnual report

Iovance Biotherapeutics : IOV COM 202 Cohort 1A ASCO 2024 Oral Presentation

Iovance Biotherapeutics : IOV COM 202 Cohort 1A ASCO 2024 Oral Presentation
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City ofUnited kingdomComunidad autonoma de catalunaUnited statesSan carlosJuan martinGuang chenSajeve thomasDurani reynalsSpeville uribeUniversitario marquAndrewjs furnessDonald lawrencePatrick terheydenBrian gastmanSylvia lee