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BioWorld - Tuesday, May 12, 2026
Home » Topics » Deals and M&A

Deals and M&A
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In rugged E3 space, Abbvie delivers Frontier justice – the good kind – via $1B-plus deal

Dec. 2, 2020
By Randy Osborne
Frontier Medicines Corp. co-founder, chairman and CEO Chris Varma told BioWorld that his firm’s deal with Abbvie Inc. happened by way of a “highly competitive process, thankfully, with multiple parties at the table,” and the tie-up means money that could “well exceed” $1 billion.
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Belgium’s Etherna and China Grand Pharma set up joint venture to tap into mRNA vaccines

Dec. 2, 2020
By Gina Lee and Elise Mak
HONG KONG and BEIJING – Hong Kong-listed China Grand Pharmaceutical and Healthcare Holdings Ltd. and Niel, Belgium-based mRNA vaccine specialist Etherna Immunotherapies NV are setting up a joint venture to develop, produce and commercialize mRNA prophylactic and therapeutic vaccines.
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Hematologic DNA blood test

Australia’s Telix to acquire Swiss Therapharm for hematology assets in AU$33M deal

Dec. 1, 2020
By Tamra Sami
PERTH, Australia – Melbourne-based Telix Pharmaceuticals Ltd. is acquiring Scintec Diagnostics GmbH subsidiary Therapharm GmbH in a deal worth AU$33 million (US$24.24 million) plus royalties. Zug, Switzerland-based Therapharm has developed a portfolio of radiolabeled diagnostic and therapeutic products, and the deal brings Telix a new targeting asset in hematology, Telix CEO Chris Behrenbruch told analysts during a Dec. 1 conference call.
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Hands holding puzzle pieces with digital globe overlay

As biopharma deals hit records in 2020, massive U.S. government funds flow into industry

Nov. 30, 2020
By Karen Carey
If there are three takeaways from this year’s dealmaking efforts, they appear to be record-setting partnerships, lackluster M&As, and massive amounts of research funding via the U.S. government.
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Doctor with brain illustration, businessman with dollar sign illustration

Herbal medicine: Sage infused with $1.5B-plus via Biogen deal

Nov. 30, 2020
By Randy Osborne
The whopper deal between Biogen Inc. and Sage Therapeutics Inc. – a global collaboration and licensing deal involving the latter’s zuranolone (also known as SAGE-217) for major depressive disorder (MDD), postpartum depression (PPD) and other psychiatric disorders, as well as SAGE-324 for essential tremor (ET) and neurological disorders – drew mixed reviews from Wall Street. And, for Biogen investors, the would-be Alzheimer’s disease (AD) therapy aducanumab remains front of mind.
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Biogen, Sage ink $1.5B-plus deal for phase III zuranolone; tremor drug, too

Nov. 30, 2020
By Randy Osborne
Software screenshot showing histology image

Agendia and Paige integrating AI-based diagnostics with genomic testing in breast cancer

Nov. 25, 2020
By Annette Boyle
New artificial intelligence capabilities will be integrated into widely used genomic testing for breast cancer under a new partnership formed by Agendia Inc. and Paige.ai. The two companies are working together to enhance the genomic information from Agendia's Mammaprint and Blueprint diagnostic tests with AI-based digital diagnostics provided by Paige with the goal of redefining precision oncology.
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Lungs

Taiho acquires Japan rights for LTI-01, Lung Tx’s therapeutic for LPE

Nov. 24, 2020
By Gina Lee
HONG KONG – Taiho Pharmaceutical Co. Ltd. has signed an exclusive license agreement with Lung Therapeutics Inc., picking up the Japanese rights to Lung Tx’s LTI-01.
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Chinese flag and microscopes

Lianbio poised for potential $70M capital injection from Pfizer

Nov. 24, 2020
By David Ho
HONG KONG – Shanghai and New Jersey-based Lianbio has landed a commitment of up to $70 million in non-dilutive capital from a new collaboration with Pfizer Inc., just weeks raising $310 million in an oversubscribed crossover financing round.
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Respiratory infection

Mesoblast licenses remestemcel-L to Novartis in deal worth up to $1.3B

Nov. 24, 2020
By Tamra Sami
PERTH, Australia – Mesoblast Ltd. inked an exclusive global licensing deal with Novartis AG for the development, manufacture and commercialization of Mesoblast’s mesenchymal stromal cell product remestemcel-L, with an initial focus on the acute respiratory distress syndrome, including that associated with COVID-19, just six weeks after the FDA issued a complete response letter for the therapy as a treatment for steroid-refractory acute graft-versus-host disease.
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