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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
214 Results
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Drug Development
Eisai Inc. Release: Lenvatinib Delays Deterioration In Certain Domains Of Quality Of Life In Patients With Unresectable Hepatocellular Carcinoma As Compared To Sorafenib In Phase III REFLECT Study
September 11, 2017
·
15 min read
Drug Development
Berg Presents Key Clinical Data At ESMO 2017 On BPM 31510 For Advanced Pancreatic Cancer Patients And BPM 31543 For Preventing Hair-Loss In Patients Treated With Chemotherapy
September 11, 2017
·
4 min read
Evolva Awarded Contract By U.S. Government To Advance Novel Pest Control Product
September 11, 2017
·
3 min read
Drug Development
AstraZeneca PLC’s Tagrisso Shows Potential As A New Standard Of Care In First-Line EGFR-Mutated Lung Cancer At ESMO 2017 Congress
September 11, 2017
·
10 min read
Policy
Bay Area’s Pulse Biosciences Withdraws 510(K) App for Its PulseTx System
September 11, 2017
·
3 min read
Bristol-Myers Squibb Release: Opdivo (Nivolumab) Demonstrates Superior Recurrence-Free Survival Versus Yervoy (Ipilimumab) For Patients With Resected High-Risk Melanoma In Phase III Checkmate -238 Study
September 11, 2017
·
1 min read
Genesis Cancercare Queensland Is First In Asia-Pacific Region To Use Elekta’s Venezia Brachytherapy Applicator
September 11, 2017
·
2 min read
Drug Development
Boehringer Ingelheim Release: Safety And Efficacy Results From The INJOURNEY Trial Investigating OFEV (Nintedanib) With Add-On Pirfenidone Provide New Data To Support Nintedanib’s Key Role In IPF
September 11, 2017
·
5 min read
Drug Development
Amgen And Allergan Present Phase III Data On Biosimilar Trastuzumab Candidate ABP 980 At The European Society For Medical Oncology 2017 Congress
September 11, 2017
·
15 min read
Drug Development
Idera Pharma Presents Positive Phase I Data For Intratumoral IMO-2125 In Combination With Ipilimumab Demonstrating An Overall Response Rate (ORR) Of 44% In Melanoma Patients Refractory To Anti-PD1 Therapy
September 11, 2017
·
9 min read
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