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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
265 Results
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Business
Caforio Out, Boerner In as BMS Sees Slight Decline with Generic Competition
The leadership shuffle comes as BMS is facing one of the steepest patent cliffs in biopharma, with exclusivity of three of its top drugs lapsing this decade.
April 27, 2023
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2 min read
·
Tristan Manalac
Drug Development
Sanofi Cleans House, Cuts Assets from Principia and Ablynx Buyouts
The French pharma drops another BTK inhibitor program from Principia and an anti-TNFa from Ablynx.
April 27, 2023
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2 min read
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Kate Goodwin
Career Advice
Are MBAs Worth the Investment?
While MBAs can reflect positively on job applicants, work experience can often be more valuable, depending on the area.
April 27, 2023
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3 min read
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Sophie Fessl
Career Advice
From Employee to Entrepreneur: How to Work for Yourself in BioPharma
To be self-employed in the life sciences, you must have a strong network and background and experience in a relevant area.
April 27, 2023
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3 min read
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Lisa Munger
Drug Development
Walgreens Launches Partnership with Prothena to Compete with CVS, Walmart
The joint venture between Walgreens and Prothena to accelerate the approval of an Alzheimer’s treatment is the latest in biotech and retail chain alliances.
April 27, 2023
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5 min read
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Natalia Mesa
FDA
Seres’ Vowst Wins FDA First-Ever Approval for Oral Microbiome Therapeutic
Vowst, the first-ever oral fecal microbiome-based therapeutic, is indicated for preventing C. diff recurrence in adults following antibacterial treatment.
April 27, 2023
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2 min read
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Tristan Manalac
Drug Development
FDA Questions Efficacy of Merck-AstraZeneca’s Lynparza Ahead of Adcomm
Merck and AstraZeneca are seeking broad approval for Lynparza in mCRPC regardless of BRCA status.
April 27, 2023
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2 min read
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Tristan Manalac
Policy
Will Biogen’s Qalsody Be a Catalyst for Gene-Specific ALS Research?
For people with, or at risk for, SOD1-ALS, the FDA’s approval of Qalsody is an important step toward advancing gene-specific research for this uniformly fatal disease.
April 27, 2023
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3 min read
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Heather McKenzie
Drug Development
Natural History Studies Drive Data Sharing, Drug Approval
Longitudinal studies that track patients’ experiences can inform and accelerate the drug approval process for rare diseases.
April 27, 2023
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5 min read
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Amanda Heidt
Drug Development
First Patient Dosed in the US in Avacta’s AVA6000 Phase 1 Clinical Study
Avacta Group plc announces that the first patient has been dosed in the US under its Investigational New Drug (IND) Application in Avacta’s phase 1 multi-centre trial evaluating the safety and tolerability of AVA6000, a novel tumour targeted form of doxorubicin and Avacta’s first therapeutic product based on its proprietary pre|CISION™ technology.
April 27, 2023
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1 min read
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