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BioWorld - Thursday, January 8, 2026
Home » Topics » Deals and M&A

Deals and M&A
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Everest lands $455M deal to hand Trodelvy rights in Asia back to Gilead’s Immunomedics

Aug. 23, 2022
By David Ho
Everest Medicines Ltd. has inked an agreement with Gilead Sciences Inc. to pass the latter’s subsidiary, Immunomedics Inc., exclusive rights to develop and commercialize Trodelvy (sacituzumab govitecan) in greater China, Singapore, Indonesia, Philippines, Vietnam, Thailand, Malaysia and Mongolia.
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Prostate cancer cells

Jemincare out-licenses prostate cancer drug to Genentech in $650M deal

Aug. 23, 2022
By Doris Yu
A subsidiary of Jiangxi Jemincare Group Co. Ltd. has out-licensed global rights to its androgen receptor degrader JMKX-002992 to Roche Holding AG and its subsidiary Genentech Inc. in a deal worth up to $650 million.
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Epithod Dx

Precision Diabetes partners with Dxgen to bring diabetes POC analyzer to US

Aug. 22, 2022
By Annette Boyle
Precision Diabetes Inc. (PDI) entered an exclusive agreement with Dxgen Corp. to introduce and distribute the Epithod Autodx point-of-care analyzer and multiple diabetes tests that run on the system within the U.S. The first available tests will include hemoglobin A1c, C-reactive protein and albumin, with the portfolio of tests expected to grow quickly.
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Everest lands $455M deal to hand Trodelvy rights in Asia back to Gilead’s Immunomedics

Aug. 19, 2022
By David Ho
Everest Medicines Ltd. has inked an agreement with Gilead Sciences Inc. to pass the latter’s subsidiary, Immunomedics Inc., exclusive rights to develop and commercialize Trodelvy (sacituzumab govitecan) in greater China, Singapore, Indonesia, Philippines, Vietnam, Thailand, Malaysia and Mongolia. Everest stands to receive up to $455 million in total consideration, including $280 million up front and up to $175 million in potential milestone payments.
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Jemincare out-licenses prostate cancer drug to Genentech in $650M deal

Aug. 19, 2022
By Doris Yu
A subsidiary of Jiangxi Jemincare Group Co. Ltd. has out-licensed global rights to its androgen receptor degrader JMKX-002992 to Roche Holding AG and its subsidiary Genentech Inc. in a deal worth up to $650 million. Shanghai Jemincare Pharmaceutical Co. Ltd. will receive $60 million up front and is eligible to collect up to $590 million for achieving development, regulatory and sales-based milestone targets.
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10-28-Boston-Science_Global-Headquarters_Marlborough,-Mass

Boston Scientific buys Obsidio in move to expand access to embolization market

Aug. 17, 2022
By Annette Boyle
Boston Scientific Corp. acquired privately held Obisidio Inc., adding the company’s gel embolic material (GEM) technology to its portfolio. GEM is a ready-to-use, semi-solid material that conforms to the vasculature in which it is placed to immediately obstruct or reduce blood flow to a tumor or abnormality or stop hemorrhaging.
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RNA illustration

Orna goes into orbit on $3.65B Merck megadeal, $221M series B round

Aug. 16, 2022
By Cormac Sheridan
Orna Therapeutics Inc., which is pioneering a novel circular RNA protein expression technology in several therapeutic areas, has achieved lift-off. The Cambridge, Mass.-based company has closed a broadly based alliance in infectious disease and oncology with Merck & Co. Inc., under which it is getting $150 million up front and up to $3.5 billion in development, regulatory and sales-based milestones. In addition, Merck, of Rahway, N.J., is investing another $100 million in Orna’s equity, as part of its $221 million series B round, which the company also disclosed on Aug. 16.
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Pheno

BD and Accelerate Diagnostics collaborate on rapid antibiotic resistance test

Aug. 15, 2022
By Annette Boyle
Becton, Dickinson and Co. and Accelerate Diagnostics Inc. joined forces to knock out sepsis and put patients on the path to recovery in hours, not days.
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Nonprofit stamp

U.S. government dominates biopharma nonprofit deals and grants

Aug. 12, 2022
By Karen Carey
Through the second week of August, BioWorld has tracked 439 bio/nonprofit deals worth $6.6 billion, with the bulk of that total coming within the last six weeks through the U.S. government purchasing more vaccines and therapies to fight COVID-19.
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Panel hails FDA stance on accelerated approval strategies

Aug. 11, 2022
By Randy Osborne
The U.S. FDA’s effort to push companies toward more and better randomized, controlled trials ahead of accelerated approvals – apparently driven by the lack of confirmatory studies done afterward – is “an important and meaningful move by the agency,” said Day One Pharmaceuticals Inc. CEO Jeremy Bender. “The industry’s history in that space has been a little mixed.” Bender’s remarks came Aug. 9 as part of a wide-ranging panel discussion hosted by analyst Robert Driscoll during the Wedbush Pacgrow Healthcare Conference.
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