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BioWorld - Sunday, June 14, 2026
Home » Topics » Deals and M&A, BioWorld

Deals and M&A, BioWorld
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James Sabry, global head of pharma partnering, Roche

Swiss pharma giants look for partnerships, not M&A as global downturn hits

March 28, 2022
By Richard Staines
The challenging financial environment of 2022 will lead to an increase in partnerships, according to representatives of the two big Swiss biopharma companies, Roche Holding AG and Novartis AG.
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China’s Nuance Pharma in-licenses Asian rights to Bavarian Nordic’s RSV vaccine in $225M deal

March 24, 2022
By Tamra Sami
Nuance Pharma Co. Ltd. signed a licensing deal with Denmark’s Bavarian Nordic A/S for rights to its MVA-BN RSV vaccine for respiratory syncytial virus (RSV) in the Chinese mainland, Hong Kong, Macau, Taiwan, South Korea and certain Southeast Asian countries. Shanghai-based Nuance plans to run its own phase I and phase III trials in China to support regulatory approval of MVA-BN RSV in China, which will be conducted separately from Bavarian Nordic's own phase III trial planned to begin in the first half of 2022.
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Dollar sign dropper and test tube

Fungi finder Lifemine brings in a series C and a GSK R&D deal

March 23, 2022
By Lee Landenberger
Fungal biosphere specialist Lifemine Therapeutics Inc. has struck a goldmine through a $175 million series C financing and an R&D collaboration allowing Glaxosmithkline plc (GSK) to use the company's platform to identify small-molecule leads.
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3D illustration of chromosomes

Wages of CIN could total $1B-plus for Volastra in synthetic-lethality BMS deal

March 21, 2022
By Randy Osborne
Volastra Therapeutics Inc., dedicated to taking aim at chromosomal instability (CIN) to design cancer drugs by way of its CINtech platform,, scored a potential $1 billion-plus agreement with Bristol Myers Squibb Co. (BMS) to find synthetic lethal targets as drug candidates.
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Edigene acquires technology from US hospital to advance hematopoietic stem cell therapy

March 18, 2022
By Doris Yu
Edigene Inc. has obtained nonexclusive, global rights to technology from Boston Children’s Hospital for technology related to increasing fetal hemoglobin levels by disrupting B-cell lymphoma/leukemia 11A (BCL11A) expression at the genomic level to treat hemoglobinopathies.
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south-korea-flag-asia.png

Everest Medicines expands IgAN deal with Calliditas to include South Korea

March 15, 2022
By Gina Lee
Everest Medicines Ltd. has acquired rights to develop and commercialize Nefecon (budesonide) for the treatment of primary IgA nephropathy in South Korea from Calliditas Therapeutics AB.
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Pfizer authorizes China Meheco Group rights to commercialize Paxlovid in China

March 14, 2022
By Doris Yu
Chinese state-owned enterprise China Meheco Group Co. Ltd. has signed a deal with Pfizer Inc. to be its mainland China partner for the commercialization of the COVID-19 pill Paxlovid (nirmatrelvir and ritonavir), which won conditional approval from China’s NMPA earlier this year.
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Nec acquires Vaximm assets for personalized T-cell cancer vaccines

March 10, 2022
By David Ho and Gina Lee

Nec Corp. has acquired all of Vaximm AG’s neoantigen program assets. Tokyo-based Nec will conduct the acquisition via its subsidiary, Nec Oncoimmunity AS.


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James Jungkue Lee, CEO, Bridge Biotherapeutics

Bridge Biotherapeutics secures second IPF candidate, targets US FDA IND by late 2022

March 10, 2022
By Gina Lee

Bridge Biotherapeutics Inc. has signed an exclusive option-to-license agreement for Cellionbiomed Inc.’s preclinical ion channel modulator, BBT-301, thus adding a second idiopathic pulmonary fibrosis (IPF) candidate to its fibrotic diseases portfolio. The company hopes to enter the clinic with the drug in the U.S. by the end of 2022.


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Brain and DNA

Novartis options Voyager AAV capsids for CNS gene therapies in potential $1.7B-plus deal

March 8, 2022
By Michael Fitzhugh
Novartis AG, an early and active player in bringing gene therapies to market, has agreed to pay Voyager Therapeutics Inc. $54 million up front and up to $1.7 billion in fees and milestone payments for options to license up to five next-generation adeno-associated virus (AAV) capsids to use as gene therapy vectors for neurological diseases.
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