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Daiichi Sankyo Company, Limited: ENHERTU Approved in the U.S. for the Treatment of Patients With Previously Treated HER2 Positive Advanced Gastric Cancer

Daiichi Sankyo Company, Limited: ENHERTU Approved in the U.S. for the Treatment of Patients With Previously Treated HER2 Positive Advanced Gastric Cancer Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and AstraZenecas ENHERTU (fam-trastuzumab deruxtecan-nxki) has been approved in the U.S. for the treatment of adult patients with locally advanced or metastatic HER2 positive gastric or gastroesophageal junction (GEJ) adenocarcinoma who have received a prior trastuzumab-based regimen...
United States Baylor University South Korea Dave Fredrickson Ronan Kelly Masashi Kawase

ENHERTU® Approved in the U.S. for the Treatment of Patients With Previously Treated HER2 Positive Ad

First HER2 directed medicine approved for patients with gastric cancer in a decadeTOKYO & MUNICH & BASKING RIDGE, N.J.--(BUSINESS WIRE)--Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) and AstraZeneca’s ENHERTU® (fam-trastuzumab deruxtecan-nxki) has been approved in the U.S. for the treatment of adult pa...
United States Baylor University South Korea Dave Fredrickson Ronan Kelly Masashi Kawase

New Research Data Across DXd ADC Portfolio at WCLC Showcases Daiichi Sankyo's Continued Commitment in Lung Cancer

New Research Data Across DXd ADC Portfolio at WCLC Showcases Daiichi Sankyos Continued Commitment in Lung Cancer will be featured as late-breaker presentation Updated TROPION-PanTumor01 results of datopotamab deruxtecan in patients with advanced NSCLC to be highlighted Biomarker analysis from phase 1 trial of patritumab deruxtecan in patients with previously treated metastatic or locally advanced EGFR mutated NSCLC to be presented Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) tod...
United States Masashi Kawase Daiichi Sankyo Daiichi Sankyo Europe Gmb Don Murphy Antoine Yver

Investegate |ObsEva SA Announcements | ObsEva SA: ObsEva Provides Update on Yselty® (Linzagolix) Clinical Development Program

ObsEva Provides Update on Yselty® (Linzagolix) Clinical Development Program   - European Medicines Agency Validates Yselty MAA for Uterine Fibroids; US NDA Planned for 1H 2021 - Phase 3 EDELWEISS 3 (Conducted in Europe and US) Study of Yselty for Treatment of Endometriosis is Progressing as Planned; Primary Endpoint Readout Expected 4Q 2021 - Phase 3 EDELWEISS 2 (Conducted in the United States) Yselty Endometriosis Study Discontinued Due to Enrollment Challenges; No Safety Concerns Identifie...
United States Shauna Dillon Brian Ocallaghan Exchange Commission Linzagolix Clinical Development Program European Medicines Agency

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