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BioWorld - Friday, July 24, 2026
Home » Authors » Karen Carey

Karen Carey

Articles

ARTICLES

Gold dollar sign inside gold cog

High value biopharma deals swell for disruptive technologies

Jan. 16, 2024
By Karen Carey
While the value of partnerships and collaborations have climbed mostly upward in recent years, the most impressive increase has been seen with deals that are worth $1 billion or more – led in 2023 with a $22 billion antibody-drug conjugate pact between Daiichi Sankyo Co. Ltd. and Merck & Co. Inc.
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Gold dollar sign inside gold cog

High value biopharma deals swell for disruptive technologies

Jan. 11, 2024
By Karen Carey
While the value of partnerships and collaborations have climbed mostly upward in recent years, the most impressive increase has been seen with deals that are worth $1 billion or more – led in 2023 with a $22 billion antibody-drug conjugate pact between Daiichi Sankyo Co. Ltd. and Merck & Co. Inc.
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Blueprint quits early lung cancer drugs, stops Gavreto marketing outside US, China

Jan. 9, 2024
By Karen Carey
Blueprint Medicines Corp. shifted away from two early clinical therapies for EGFR-mutant non-small-cell lung cancer and dropped development and commercialization of lung and thyroid cancer drug Gavreto (pralsetinib) for areas outside of the U.S. and greater China, reducing its operating expenses, as it prepares for increasing Ayvakit sales and prioritizes development of other assets.
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Novo Nordisk joins Flagship’s Omega and Cellarity in obesity, MASH, deals

Jan. 4, 2024
By Karen Carey
A deal crafted in May 2022 between Novo Nordisk A/S and Flagship Pioneering has culminated into two separate research collaborations that are worth up to $532 million each in up-front and milestone payments for Omega Therapeutics Inc. and Cellarity Inc.
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Art concept for gene therapy research

Voyager sets sail once again with Novartis in $1.3B gene therapy pact

Jan. 2, 2024
By Karen Carey
Nearly two years after Novartis AG signed a $1.7 billion deal for options to Voyager Therapeutics Inc.’s adeno-associated virus capsids for central nervous system disorders, the Basel, Switzerland-based company secured rights to develop gene therapies for Huntington’s disease and spinal muscular atrophy in a licensing agreement potentially worth $1.3 billion.
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M&A cityscape

Billion-dollar M&As: Bristol Myers buying Rayzebio; Astrazeneca taking over Gracell

Jan. 2, 2024
By Karen Carey
Two big pharma firms placed high offers on Dec. 26 to acquire companies focused on radiopharmaceuticals and cell therapies in what Evercore ISI analysts are calling a “good sign for the end of the year.”
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Top Trends Therapeutics, pill, syringe

Obesity/overweight opportunities drive R&D and funding

Dec. 28, 2023
By Karen Carey
If there is one therapeutic area for which numerous biopharma companies and investors have shown increasing amounts of interest in 2023, it is obesity through follow-on glucagon-like peptide-1 receptor agonists, as well as combination and solo efforts with other potential mechanisms. Analysts have suggested the obesity market (which includes overweight individuals) could grow to more than $50 billion by 2030. At least.
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M&A cityscape

Billion-dollar M&As: Bristol Myers buying Rayzebio; Astrazeneca taking over Gracell

Dec. 27, 2023
By Karen Carey
Two big pharma firms placed high offers on Dec. 26 to acquire companies focused on radiopharmaceuticals and cell therapies in what Evercore ISI analysts are calling a “good sign for the end of the year.”
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Ionis’ Wainua approved in US for rare disease hATTR-PN

Dec. 22, 2023
By Karen Carey
A new self-injectable therapy for polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN) will be available in January 2024 now that the U.S. FDA has approved Ionis Pharmaceuticals Inc.’s Wainua (eplontersen), a ligand-conjugated antisense oligonucleotide.
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Merck’s gefapixant gets second CRL for chronic cough

Dec. 21, 2023
By Karen Carey
Receiving a second complete response letter (CRL) from the U.S. FDA for gefapixant to treat refractory and unexplained chronic cough – an indication for which there are no approved treatments in the U.S., Merck & Co. Inc. said it is reviewing the agency’s feedback to determine the next steps, if any, for the oral selective P2X3 receptor antagonist.
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View All Articles by Karen Carey

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