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Latest Pharma-News

First and only ingestible event marker (the ID-Cap® System)approved by U.S. FDA

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Latest Pharma-News

Moberg Pharma meets primary endpoint for MOB-015 (topical terbinafine) in a phase 3 study for the treatment of Onychomycosis

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U.S. FDA approved Fast Track designation for Equillium’s itolizumab (EQUALISE Phase 1b study )for the treatment of lupus nephritis

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Clinical Data Management

Important data points in Protocol for CRFs Creation (CDM Prospective):

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Clinical Data Management

Parts of a clinical trial protocol and Clinical Data Management (CDM) prospective to review

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Only treatment approved in the US for relapsed or refractory hairy cell leukemia Approved by FDA at ASH 2019

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Amgen’s AVSOLA™ received FDA approval for AVSOLA™ (infliximab-axxq), For The Same Indications As Remicade® (infliximab)for the treatment of Rheumatoid Arthritis, Crohn’s Disease, Ulcerative Colitis,...

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ViiV Healthcare submits New Drug Application to the US FDA for fostemsavir, an investigational, first-in-class attachment inhibitor for the treatment of HIV in adults

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FDA authorizes marketing of diagnostic test cobas vivoDx that uses novel technology to detect Methicillin-resistant Staphylococcus aureus (MRSA) bacteria

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First investigational drug therapy for liver disease non alcoholic steatohepatitis (NASH) awaiting FDA approval

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Latest Pharma-News

Data fron XOSPATA® in FLT3 Mutation-Positive Relapsed/Refractory Acute Myeloid Leukemia at the 2019 American Society of Hematology Annual Meeting

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First generics of Gilenya approved by FDA for the treatment of relapsing forms of multiple sclerosis (MS) in adult patients

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