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Foundation Medicine and PMV Pharma Announce Collaboration to Develop Companion Diagnostic for Rezatapopt, a First-In-Class, Investigational, Selective p53 Y220C Reactivator

BOSTON & PRINCETON, N.J. (BUSINESS WIRE) May 29, 2024

United statesNew jerseyArnold levineFoundationone cdxKathy vincentTroy schurrDanielle johnsTim smithPharmaceuticals incFoundation medicine incGreig communicationsFoundation medicineFlatiron healthDrug administrationFoundation medicine commercial tissue or hemeFoundation medicine clinico

AnHeart Therapeutics and Foundation Medicine Announce Collaboration to Develop Tissue-Based and Liquid-Based Companion Diagnostics for Taletrectinib, a ROS1 Inhibitor

AnHeart Therapeutics and Foundation Medicine Announce Collaboration to Develop Tissue-Based and Liquid-Based Companion Diagnostics for Taletrectinib, a ROS1 Inhibitor
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United statesNew yorkTroy schurrFoundationone cdxFoundation medicineFoundation medicine announce collaboration to develop tissueChina national medical products administrationDrug administrationFoundation medicine incHeart therapeuticsFoundation medicine announce collaborationDevelop tissue basedLiquid based companion diagnosticsBreakthrough therapy designationChief biopharma business officerIntended use

Foundation Medicine, AnHeart Therapeutics to Develop CDx for NSCLC Therapy

Foundation Medicine, AnHeart Therapeutics to Develop CDx for NSCLC Therapy
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FDA Approves Companion Diagnostic for Capivasertib Plus Fulvestrant in Advanced HR+/HER2–Breast Cancer

The FDA has approved the FoundationOne® CDx for use as a companion diagnostic to identify patients with advanced hormone receptor–positive, HER2-negative advanced breast cancer who may be eligible for treatment with the combination of capivasertib and fulvestrant.

Shehzin tietjenAstrazeneca truqapTroy schurrFoundationone cdxFoundation medicineLiving beyond breast cancerPrecision medicine in oncologyBreast cancer

U S FDA Approves FoundationOne®CDx as a Companion Diagnostic for AstraZeneca s Truqaptm (capivasertib) in combination with Faslodex® (fulvestrant) to Identify Patients with HR-Positive, HER2-Negative Advanced Breast Cancer

U S FDA Approves FoundationOne®CDx as a Companion Diagnostic for AstraZeneca s Truqaptm (capivasertib) in combination with Faslodex® (fulvestrant) to Identify Patients with HR-Positive, HER2-Negative Advanced Breast Cancer
lelezard.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from lelezard.com Daily Mail and Mail on Sunday newspapers.

Astrazeneca truqapFoundationone cdxShehzin tietjenTroy schurrAstrazeneca truqaptmDrug administrationFoundation medicine incProduct serviceFoundation medicineCompanion diagnosticIdentify patientsNegative advanced breastChief biopharma business officerAssociate directorCorporate relationsLiving beyond breast