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EC approves Roche’s Perjeta for post-surgery treatment of HER2-positive early breast cancer at high…

Jun 4, 2018
Roche announced that the European Commission (EC) has approved Perjeta (pertuzumab) in combination with Herceptin (trastuzumab) and chemotherapy (the Perjeta-based regimen) for…
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Alcami to Become Industry Leading Platform CDMO Following Acquisition by Madison Dearborn Partners

Jun 4, 2018
Alcami Corporation announced that it has reached an agreement to be acquired by Madison Dearborn Partners. MDP will acquire a majority ownership position in Alcami from existing…
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PPD and NeoGenomics Forming Global Strategic Alliance for Pathology and Molecular Testing Solutions

Jun 4, 2018
Pharmaceutical Product Development (PPD) and NeoGenomics Laboratories are forming a strategic alliance to provide a seamless and fully integrated global pathology and molecular testing…
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Pharmaceutical Microbiology West Coast Conference & Exhibition takes place in less than a week

Jun 1, 2018
SMi Reports: There are only 3 places left, in 1 week leading industry experts within the microbiology community will be meeting in San Diego at SMi’s largest Pharmaceutical Microbiology…
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FORMA Therapeutics and HitGen Initiate Multiyear Research Collaboration

Jun 1, 2018
FORMA Therapeutics and HitGen announced a multiyear research collaboration and license agreement to build and screen proprietary DNA-encoded libraries (DELs). Through this collaborative…
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Aptar Pharma and Propeller Health Partner to Develop Digital Medicine Platform Across Therapeutic…

Jun 1, 2018
Aptar Pharma announced plans to collaborate on the launch of a comprehensive platform to develop digital medicines for multiple therapeutic areas and diseases. The digital medicine…
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Daiichi Sankyo Announces Launch of Immune-mediated Inflammatory Diseases Consortium for Drug…

Jun 1, 2018
Daiichi Sankyo Company announced the launch of Immune-mediated Inflammatory Diseases Consortium for Drug Development (hereafter, the consortium) to research and discover drugs for…
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FDA expedites review of Novartis drug Promacta for first-line severe aplastic anemia (SAA)

Jun 1, 2018
Novartis announced that the US Food and Drug Administration (FDA) has accepted the company's supplemental New Drug Application (sNDA) and granted Priority Review designation to Promacta…
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Arrowhead Completes Enrollment in Single Dose Portion of Phase 1/2 Study of ARO-HBV

May 31, 2018
Arrowhead Pharmaceuticals announced that it has completed enrollment and dosing of all 5 planned cohorts of healthy adult volunteers in the single-ascending dose portion of its ongoing…
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Pfizer Announces FDA Approves XELJANZ (tofacitinib) for the Treatment of Moderately to Severely…

May 31, 2018
Pfizer Inc. announced that the United States (U.S.) Food and Drug Administration (FDA) approved XELJANZ (tofacitinib) 10 mg twice-daily (BID) for at least eight weeks, followed by…
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Press Releases

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IQ MPS Leaders to Share Industry Progress on Advancing In…

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