Obesity & Weight Loss Drug Development Summit Leaderboard
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BiomX Raises $32 Million in Series B Financing

Feb 21, 2019
BiomX Ltd. announced the closing of a $32 million series B equity financing. The financing was led by existing investors OrbiMed, Johnson & Johnson Innovation – JJDC, Inc., Takeda…
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NanoSphere Signs Definitive Licensing Agreement in Oregon

Feb 20, 2019
NanoSphere Health Sciences Inc. announced the signing of a definitive Licensing Agreement with Oregon cannabis company Cascade Pure, LLC. The Agreement gives Cascade Pure the exclusive…
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Knight Therapeutics and Triumvira Immunologics Triumphantly Announce Secured Bridge Loan &…

Feb 20, 2019
Knight Therapeutics Inc. announced it has entered into a secured loan and exclusive License Agreement with privately-held Triumvira Immunologics. The US$5 million secured loan has a…
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Indivior Announces Launch of SUBOXONE (buprenorphine and naloxone) Sublingual Film Authorized…

Feb 20, 2019
Indivior PLC announced that its U.S. affiliate, Indivior Inc., has launched an authorized generic version of SUBOXONE (buprenorphine and naloxone) Sublingual Film (CIII) in the U.S. The…
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Torque Announces Clinical Trial Collaboration with Merck

Feb 20, 2019
Torque, a clinical-stage immuno-oncology company developing first-in-class Deep Primed T Cell Therapeutics to direct immune power deep within the tumor microenvironment, announced that…
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Pre-Filled Syringes – Chemical Compatibility and Design Strategies

Feb 20, 2019
At SMi’s 2019 Pre-Filled Syringes East Coast USA Conference, industry leaders will meet in Boston to share their insights on best design practice, drug compatibility within the whole…
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FDA grants Priority Review to Roche’s personalised medicine entrectinib

Feb 20, 2019
Roche announced that the US Food and Drug Administration (FDA) has accepted the company’s New Drug Applications (NDAs) and granted Priority Review for entrectinib for the treatment of…
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FDA grants priority review to Roche’s polatuzumab vedotin in previously treated aggressive lymphoma

Feb 20, 2019
Roche announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s Biologics License Application (BLA) and granted Priority Review for polatuzumab vedotin in…
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FDA agrees to review AbbVie’s upadacitinib in rheumatoid arthritis

Feb 20, 2019
AbbVie has announced that the U.S. Food and Drug Administration (FDA) has accepted for priority review its New Drug Application (NDA) for upadacitinib for the treatment of adult…
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Pfizer and Lilly Announce Top-line Results From Phase 3 Study of Tanezumab in Chronic Low Back Pain

Feb 20, 2019
Pfizer Inc. and Eli Lilly and Company announced positive top-line results from a Phase 3 study evaluating tanezumab in patients with moderate-to-severe chronic low back pain (CLBP). In…
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