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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
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Drug Development
Pfizer’s JAK Inhibitor Xeljanz Racks Up Another FDA Win
The FDA’s approval of Xeljanz is based on Pfizer’s Phase III multicenter, double-blind, placebo-controlled study. Here are more details about the study.
December 15, 2021
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2 min read
·
Vanessa Doctor, RN
Drug Development
Lilly UC Treatment Holds Edge in Maintenance Study, Setting Up BLA
These results set Lilly up well to submit a Biologics License Application (BLA) in the first half of 2022.
December 15, 2021
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3 min read
·
Sreetama Dutt
Drug Development
Notch Another Win for AbbVie’s Rinvoq, This Time in Psoriatic Arthritis
The FDA approved the latest indication for Rinvoq (upadacitinib) based on data from two Phase III studies, SELECT-PsA 1 and SELECT-PsA 2.
December 15, 2021
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2 min read
·
Alex Keown
Genetown
Mythic Therapeutics Scores $103 Million to Make “Safer and Smarter” ADCs
Mythic Therapeutics has roared out of the gate with a $103 million Series B financing round that will support “safer and smarter” next generation of antibody-drug conjugates (ADCs).
December 15, 2021
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3 min read
·
Alex Keown
Drug Development
Omicron Surges Across the World While Vaccines Struggle to Contain It
Although it’s not yet clear how dangerous the Omicron variant of COVID-19 actually is, it clearly is very infectious and rates are rising in the U.S. and around the world.
December 15, 2021
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6 min read
·
Mark Terry
Business
It’s Back to the Drawing Board for Generation Bio’s Hemophilia A Program
Generation Bio’s stock plummeted 54% to $6.35 yesterday after it reported in an SEC filing that its hemophilia A therapy data in mice couldn’t be duplicated in non-human primate studies.
December 15, 2021
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2 min read
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Mark Terry
Career Advice
How to Answer Some Tricky Interview Questions
It’s no secret that employers ask tricky interview questions. But what do you do if you find yourself fumbling for words to answer these tricky questions?
December 15, 2021
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4 min read
·
Hannah Harshman
BioMidwest
Eli Lilly’s Two-Year Ambition Includes Alzheimer’s Approvals
Eli Lilly and Company’s projections for next year exceed Wall Street projections for the company, predicting 2022 revenue of $27.8 billion to $28.3 billion.
December 15, 2021
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3 min read
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Mark Terry
Drug Development
FDA Greenlights BMS’s Orencia for Acute GVHD – Partly on RWE
The FDA said Orencia is the first drug approved as prophylaxis for aGVHD prevention that included real-world evidence as one component of clinical efficacy.
December 15, 2021
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2 min read
·
Alex Keown
Business
Money on the Move: December 8 – 14
During a season of giving, investors were extra generous to these biotech companies this week.
December 15, 2021
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3 min read
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Kate Goodwin
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