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BioWorld - Saturday, May 9, 2026
Home » licensing

Articles Tagged with ''licensing''

Promising results drive push for Paxlovid compulsory license

Dec. 7, 2021
By Mari Serebrov
Although Pfizer Inc.’s COVID-19 oral antiviral candidate, Paxlovid (PF-07321332; ritonavir), has yet to be authorized anywhere, the push for compulsory licensing of the drug has begun.
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DNA data illustration

For up to $1.1B, Selecta joins with Takeda in AAV gene therapies

Oct. 5, 2021
By Lee Landenberger
Selecta Biosciences Inc. joined a licensing agreement with Takeda Pharmaceutical Co. Ltd. to develop AAV-driven gene therapies for two lysosomal storage disorders that could bring Watertown, Mass.-based Selecta up to $1.124 billion. The payments depend upon hitting development or commercial milestones. Selecta is also receiving an undisclosed up-front payment and is eligible for tiered royalties on commercial sales.
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KRAS protein

Innovent acquires KRAS G12C candidate from Genfleet in $312M deal

Sep. 7, 2021
By Doris Yu
Innovent Biologics Inc. has inked a $312 million licensing deal for the development and commercialization of Genfleet Therapeutics Inc.’s KRAS G12C inhibitor, GFH-925, in mainland China, Hong Kong, Macau and Taiwan. Innovent also has additional option-in rights for global development and commercialization.
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Handshake with DNA, molecules

Biogen catches up in MS with nearly $1B deal for Innocare’s orelabrutinib

July 13, 2021
By Elise Mak
In a deal that could be worth up to $937.5 million, Biogen Inc. licensed rights to phase II-stage, brain-penetrant BTK inhibitor orelabrutinib from Innocare Pharma Ltd. for the treatment of multiple sclerosis (MS) and autoimmune diseases. It’s the first mega out-licensing deal for the Chinese firm, which will receive $125 million up front and is eligible to receive up to $812.5 million in potential development milestones and commercial payments, plus tiered royalties in the low to high teens on potential future net sales.
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Antengene, Calithera reach deal for CD73 inhibitor

May 25, 2021
By Elise Mak and Sergio Held
BEIJING, China and SANTANDER, Spain – Antengene Corp. and Calithera Biosciences Inc. entered a worldwide exclusive license agreement to develop and market the CD73 inhibitor CB-708 (ATG-037), as part of a push to use the small-molecule inhibitor to grab significant market share in Asia Pacific and global markets.
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Stomach and intestine

Lianbio licenses Landos’ LANCL2- and NLRX1-targeted candidates in $218M deal for UC and CD

May 18, 2021
By Elise Mak
Shanghai and New Jersey-based Lianbio Co. Ltd. has made its second in-licensing deal in a week. This time, it obtained rights for omilancor and NX-13, both under development by Landos Biopharma Inc. for the potential treatment of ulcerative colitis (UC) and Crohn’s disease (CD) – plus eosinophilic esophagitis, for omilancor – in greater China, South Korea and seven ASEAN countries as part of a $218 million deal.
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Chinabio Partnering Forum: Competition in dealmaking intensifies for Chinese biopharma

May 14, 2021
By Elise Mak
While partnering activities reached new highs in 2020, Chinese biopharma players found it more difficult to snatch good deals in a more competitive landscape. They now need to act faster and do more preparation work to seize partnering opportunities, panelists said at the Chinabio Partnering Forum.
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Pregene licenses BCMA CAR T-cell therapy to Dr. Reddy’s in $162.5M deal

May 11, 2021
By Elise Mak

Shenzhen Pregene Biopharma Co. Ltd. has outlicensed its internally developed anti-BCMA CAR T-cell therapy candidate, PRG-1801, to Indian pharma giant Dr. Reddy's Laboratories Ltd. in a $162.5 million deal to develop and commercialize it in India.


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Canbridge inks deal for Logicbio’s gene therapy candidates

May 4, 2021
By Elise Mak and David Ho
HONG KONG – Canbridge Pharmaceuticals Inc. signed a collaboration and licensing agreement that could be worth $591 million, gaining global rights to develop, manufacture and commercialize gene therapy candidates from Logicbio Therapeutics Inc. for the treatment of Fabry and Pompe diseases. The candidates are based on Logicbio’s adeno-associated virus (AAV) sL65, the first produced from its Saavy capsid development platform.
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Kazia out-licenses ovarian cancer drug to Oasmia to focus on glioblastoma

March 2, 2021
By Tamra Sami
PERTH, Australia – Sydney-based Kazia Therapeutics Ltd. has out-licensed its ovarian cancer drug, Cantrixil (TRX-E-002-1), to Sweden’s Oasmia Pharmaceutical AB in a deal worth up to $46 million. Oasmia will pay $4 million up front, and development milestones worth up to $42 million and double-digit sales royalties.
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