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BioWorld - Thursday, January 29, 2026
Home » Topics » Deals and M&A, BioWorld

Deals and M&A, BioWorld
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Globe in DNA helix

Sarepta strengthens itself in U.S. and stretches worldwide with Roche deal, gaining $1.5B up front

Dec. 23, 2019
By Lee Landenberger
In a move that Sarepta Therapeutics Inc.’s president and CEO, Doug Ingram, called “transformational” for the company and “the largest licensing transaction in cell or gene therapy history,” Sarepta granted Roche Holding AG exclusive commercial rights outside the U.S. for SRP-9001, its gene therapy for Duchenne muscular dystrophy (DMD).
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U.S.-China capsule

Tracon buys rights to subcutaneous PD-L1 antibody from China’s 3D Medicines and Alphamab

Dec. 23, 2019
By Elise Mak
BEIJING – U.S. biotech Tracon Pharmaceuticals Inc., of San Diego, has in-licensed from Chinese drugmakers 3D Medicines (Beijing) Co. Ltd. and Jiangsu Alphamab Biopharmaceuticals Co. Ltd. the rights to develop envafolimab, a subcutaneous PD-L1 antibody, to treat soft tissue sarcoma in North America.
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Sarepta, Roche in $1.15B deal for DMD drug outside the U.S.

Dec. 23, 2019
By Lee Landenberger

Roche inks $793M immunometabolism deal with Rheos Medicines

Dec. 19, 2019
By Michael Fitzhugh
Roche Holding AG took an interest in immunometabolism specialist Rheos Medicines Inc. even before its March 2018 launch. Now, less than two years later, it has tapped Cambridge, Mass.-based company, founded by Third Rock Ventures, to identify and develop an undisclosed number of new therapies for autoimmune and inflammatory disease.
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Handshake, businessmen holding dollar sign, lightbulb

$120M up front: Takeda makes a big bet on Turnstone’s preclinical vaccinia immunotherapy platform

Dec. 19, 2019
By Cormac Sheridan
Turnstone Biologics Inc. has found a major backer for its preclinical vaccinia-based oncolytic virus platform for cancer immunotherapy. Takeda Pharmaceutical Co. Ltd. is paying $120 million in up-front, near-term milestones and equity investment and could pay $900 million more in development, regulatory and commercial milestones to enter a strategic alliance with the New-York-based firm.
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Syros, GBT in multimillion-dollar deal to treat sickle cell, beta-thalassemia

Dec. 18, 2019
By Lee Landenberger
Syros Pharmaceuticals Inc. and Global Blood Therapeutics Inc. (GBT) agreed to a discovery, development and commercialization deal to treat sickle cell disease (SCD) and beta-thalassemia. GBT, of South San Francisco, Calif., will pay Syros $20 million up front and fund up to $40 million in preclinical research for at least three years, with the goal of identifying targets and discovering drugs to induce fetal hemoglobin.
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Brain, illustrating pain/injury

Neurotrauma Sciences exercises an option with Emory University

Dec. 12, 2019
By Lee Landenberger
Neurotrauma Sciences LLC and Emory University’s Institute for Drug Development entered a license agreement for patents and technology invented at the school, enlarging a deal the two cut about a year ago.
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Sunshine’s better on the other side

Numab banks $15M equity investment in 3Sbio immuno-oncology pact

Dec. 12, 2019
By Cormac Sheridan
DUBLIN – Numab Therapeutics AG is banking an equity investment of CHF15 million (US$15.2 million) from its latest Asian partner, Sunshine Guojian Pharmaceutical (Shanghai) Co. Ltd., as part of a broad alliance to develop up to five multispecific antibodies from three programs based on Numab’s Match platform.
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Tuberculosis

Quratis sells TB vaccine worth $1.1B to Indonesia’s state-run company

Dec. 11, 2019
By Jihyun Kim
HONG KONG - South Korean biopharmaceutical company Quratis Inc. and Indonesia’s state-run company, Bio Farma PT, have entered a term sheet agreement to develop and commercialize Quratis’ tuberculosis (TB) vaccine, QTP-101, for adults and adolescents. The total amount of the deal is around ₩1.2 trillion (US$1.1 billion), according to the Seoul-based company.
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Chess board and pieces, blocks spelling out M&A

Bruton soup’s on: Merck paying $2.7B for Arqule, Aptose bubbles as Lilly data cool at ASH

Dec. 9, 2019
By Randy Osborne
Arqule Inc. CEO Paolo Pucci said the firm was “limited in what we can comment [on] for the time being” in connection with Merck & Co. Inc.’s deal to pay about $2.7 billion in cash for the company. “There is no better model for bringing a drug faster into the hands of patients and caregivers than the example of Keytruda. I will leave it at that.” Merck’s Keytruda (pembrolizumab), a human PD-1-blocking antibody was first approved in September 2014 for advanced melanoma. The label has been widely expanded since. 
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