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BioWorld - Thursday, February 26, 2026
Home » Topics » Deals and M&A

Deals and M&A
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Acquisition puzzle

Telix to buy Artms for $82M to shore up radioisotope supply

March 5, 2024
By Tamra Sami
In a move to build up its dominance in the radiopharma market, Telix Pharmaceuticals Ltd. said it plans to acquire radioisotope production technology firm Artms Inc. and its advanced cyclotron-based isotope production platform, manufacturing plant and stockpile of ultra-pure rare metals.
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Gastrointestinal

Everzom signs license agreement with Erganeo for Evergel

March 5, 2024
Everzom SAS, a CNRS/Université Paris Cité spin-off, has signed a second exclusive license agreement with Erganeo SAS for the development of Evergel, an exosome drug candidate for fistulas and fibrosis of the digestive tract.
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Biocom 2024: Pharma looking for deals to be done

March 4, 2024
By Brian Orelli
With valuations heading higher, pharmaceutical companies are looking to make deals. “The M&A environment has kind of woken up a little bit,” Jay Stamatis, vice president and head of business development and acquisitions at Abbvie Inc., told the audience at Biocom California’s Global Life Science Partnering & Investor Conference.
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Nonprofit stamp
Biopharma nonprofit deals and grants 2023

Biopharma grants soar to $6.11B in 2023 while nonprofit deal value falls by 90%

March 1, 2024
By Amanda Lanier
Biopharma grants maintained their upward trajectory throughout 2023, culminating in a nearly 67% increase in value compared to 2022, mirroring the trend observed in October. Conversely, nonprofit deal value witnessed a continued year-over-year decline, falling by more than 90% in value.
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Takeda, Biological E. partner to widen global access to Qdenga

Feb. 28, 2024
By Tamra Sami
In a move to widen global access to its Qdenga dengue vaccine, Takeda Pharmaceutical Co. Ltd. is partnering with India’s Biological E. Ltd. to manufacture Qdenga (TAK-003).
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Deal activity continues as OSE, Abbvie ink $713M partnership

Feb. 28, 2024
By Jennifer Boggs
OSE Immunotherapeutics SA disclosed a $713 million deal with Abbvie Inc. for preclinical-stage monoclonal antibody OSE-230, a potentially first-in-class therapy for treating a range of inflammatory diseases, while Idorsia Ltd. found a partner for two phase III-stage assets in Viatris Inc., as dealmaking continues strong in 2024.
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Alteogen headquarters

Alteogen names MSD as partner in revised, potential $3.8B+ deal

Feb. 27, 2024
By Marian (YoonJee) Chu
In a surprise reveal that propelled stocks by 25%, Alteogen Inc., of Daejeon, South Korea, named MSD International Business GmbH as its counterpart in a near-$4 billion technology transfer agreement inked in 2020, while upping terms of the deal.
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Alteogen headquarters

Alteogen names MSD as partner in revised, potential $3.8B+ deal

Feb. 23, 2024
By Marian (YoonJee) Chu
In a surprise reveal that propelled stocks by 25%, Alteogen Inc., of Daejeon, South Korea, named MSD International Business GmbH as its counterpart in a near-$4 billion technology transfer agreement inked in 2020, while upping terms of the deal.
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Tentarix joins a $64M collaboration with Abbvie

Feb. 22, 2024
By Lee Landenberger
In its second big collaboration of the past six months, privately held Tentarix Biotherapeutics LP plans to discover and develop biologics for treating oncology and immunology indications with Abbvie Inc. The deal comes at a time of change at Abbvie, which is getting a new CEO, watching the marketplace erosion of bestselling Humira (adalimumab) and digesting two major acquisitions at a cost of billions.
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Blue capsules

Rigel takes on US marketing of Blueprint’s Gavreto

Feb. 22, 2024
By Karen Carey
Blueprint Medicines Corp. found a new U.S. commercialization home for Gavreto (pralsetinib) through an agreement with Rigel Pharmaceuticals Inc. potentially worth $117.5 million, now that Roche Holding AG has relinquished all rights. The product, a once-daily oral small-molecule kinase inhibitor of wild-type RET (rearranged during transfection) and oncogenic RET fusions, received accelerated approval in 2020 by the U.S. FDA, under priority review and with orphan drug designation, to treat adults with metastatic RET fusion-positive non-small-cell lung cancer.
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