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Shire and Parion Sciences Enter into a Collaborative License Agreement to Advance P-321 for…

May 2, 2017
Shire plc and Parion Sciences, Inc. announced they have entered into an agreement granting Shire exclusive worldwide rights to develop and commercialize P-321. Shire will lead…
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Agreement to buy F-Star Alpha between Bristol-Myers Squibb and F-star Alpha terminated

May 1, 2017
Agreement to buy F-Star Alpha and its lone asset, FS102 between Bristol-Myers Squibb and F-star Alpha has been terminated. Bristol-Myers Squibb and F-star Alpha, entered into an…
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Sorrento Therapeutics successfully completes acquisition of Virttu Biologics

May 1, 2017
Sorrento Therapeutics announced that it has successfully completed the transaction for acquisition of Virttu Biologics. In consideration for the acquisition, Virttu equity holders…
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Dr. Wilson appointed TAPIMMUNE President after Dr. Bonfiglio’s resignation

May 1, 2017
TAPIMMUNE announced that Dr. Wilson has been appointed President after Dr.John Bonfiglio’s resigned as Chief Operating Officer, President and director of TapImmune Inc. to pursue other…
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FDA approves Rydapt in combination with Chemotherapy for treatment of AML

May 1, 2017
The U.S. FDA approved Rydapt (midostaurin) in combination with Chemotherapy for the treatment of adult patients with newly diagnosed AML (acute myeloid leukemia) who have a specific…
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MedMira receives CE Marks on its syphilis/HIV rapid test

May 1, 2017
MedMira has received CE mark on its syphilis/HIV rapid test, Multiplo TP/HIV, this approval allows company to market and distribute the multiplex rapid test throughout the European…
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Allergan completes acquisition of ZELTIQ Aesthetic

May 1, 2017
Allergan announced that it has completed the acquisition of ZELTIQ Aesthetics for $2.4 billion cash. ZELTIQ stockholders approved the transaction during the meeting held on April 27,…
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enGene appoints Theresa Podrebarac as CMO

May 1, 2017
enGene announced that Theresa Podrebarac, has been appointed as the  Chief Medical Officer of the company. He will be responsible for designing and executing clinical development plan…
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FDA grants Pfizer’s Lorlatinib breakthrough designation for NSCLC

Apr 29, 2017
The US Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to Pfizer’s lorlatinib for the treatment of patients with anaplastic lymphoma kinase…
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Takeda, Harrington to advance development of rare disease therapeutics

Apr 29, 2017
Takeda Pharmaceutical has entered into a multi-year partnership with Harrington Discovery Institute at University Hospitals in Cleveland, Ohio to advance the development of rare disease…
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