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FDA Accepts Rigel’s New Drug Application for TAVALISSE

Jun 19, 2017
Rigel Pharmaceuticals announced the U.S. Food and Drug Administration (FDA) has filed its New Drug Application (NDA) for the use of TAVALISSE™ (fostamatinib disodium) in patients with…
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Lannett Announces Approval For Amantadine Hydrochloride Capsules USP, 100 mg

Jun 19, 2017
Lannett Company announced that it received approval from the U.S. Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Amantadine Hydrochloride Capsules…
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Boehringer presents phase III results of adalimumab biosimilar candidate to HUMIRA

Jun 16, 2017
Boehringer Ingelheim announced results from the pivotal Phase III VOLTAIRE-RA study, confirming that its adalimumab biosimilar candidate BI 695501 and HUMIRA have similar efficacy,…
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Johnson & Johnson Announces Completion of Acquisition of Actelion

Jun 16, 2017
Johnson & Johnson announced the completion of the acquisition of Actelion Ltd for a total purchase price of approximately $30 billion in cash. The acquisition was completed through…
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Baxter Announces Agreement with Dorizoe Lifesciences to Further Expand Generic Injectables Pipeline

Jun 15, 2017
Baxter International announced an agreement with Dorizoe Lifesciences Limited (Dorizoe), a full-service global contract research and development (R&D) organization, that will…
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Probiodrug announces encouraging results of the Phase 2a SAPHIR Study

Jun 15, 2017
Probiodrug has reported positive results for its PQ912 candidate in a Phase 2a SAPHIR study in early Alzheimer’s disease (AD) patients. The SAPHIR study is the first clinical trial…
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Pfizer Receives Commercialization Rights in Europe for CRESEMBA

Jun 15, 2017
Pfizer and Basilea Pharmaceutica announced that they have entered into an agreement whereby Pfizer will be granted the exclusive commercialization rights in Europe to CRESEMBA…
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Generon announces the initiation of a Phase 1 Clinical Trial for A-337

Jun 15, 2017
Generon Corporation announced the initiation of a clinical trial for A-337, a CD3-activating bi-specific antibody targeting EpCAM, in Australia. This is a “Phase I, Open-label,…
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LEO Pharma Starts Phase 3 Clinical Study for Tralokinumab in Atopic Dermatitis

Jun 15, 2017
LEO Pharma today announced that the first patients have been dosed in a phase 3 clinical study of tralokinumab. Tralokinumab is an investigational human monoclonal antibody that…
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SGS Expands Extractables and Leachables Testing Capabilities at its Shanghai Facility

Jun 15, 2017
SGS announced that it has significantly increased its capabilities to undertake extractables and leachables (E&L) testing at its Shanghai, China, laboratory. Its investment…
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