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Allergan plc announces data at ASM Microbe Highlight In Vitro Antimicrobial Activity of AVYCAZ

Allergan plc committed to developing new treatment options for infectious diseases, today presented new data highlighting the in vitro activity of AVYCAZ® against several species of Gram-negative pathogens, including certain strains of Klebsiella pneumoniae carbapenemase (KPC)-producing Enterobacteriaceae and Pseudomonas...

Medipak Systems Open House at the new premises of Dividella AG

Dividella AG, a Medipak Systems company, welcomed guests to the two-day pharma event in its new premises in Grabs, Switzerland. As part of the extension of its capacity, Dividella has leased additional premises in the adjacent...

Quotient Clinical hosts formulation development and drug delivery seminar series

Quotient Clinical, the Translational Pharmaceutics company, is holding a series of formulation development and drug delivery seminars this June and July. The seminars will take place at major life science hubs in the UK and USA,...

FDA Accepted Charleston Laboratories, Inc. and Daiichi Sankyo’s New Drug Application (NDA) for CL-108

Charleston Laboratories, Inc. and Daiichi Sankyo, Inc. announced that the U.S. FDA has accepted for review the New Drug Application (NDA) for CL-108 for the relief of moderate to severe pain while preventing or reducing the associated opioid-induced nausea...

Ziarco Pharma Ltd reports positive Phase 2a study results with ZPL-389

Ziarco Pharma Ltd a biopharmaceutical company focusing on the development of novel drugs for the treatment of inflammatory skin disorders, today announces positive, full results from its first Phase 2a proof of concept study with ZPL-389 in adults. ...

Teva Pharmaceutical Inc suspends marketing for Zecuity in US

Teva Pharmaceutical Industries, Ltd. announced that it will voluntarily suspend sales, marketing and distribution of ZECUITY® (sumatriptan iontophoretic transdermal system). Teva has received post-marketing reports of application site reactions described as burns and scars in patients...

ViiV Healthcare announces FDA approval to lower the weight limit for dolutegravir in children and adolescents living with HIV

ViiV Healthcare announced that the US FDA has approved a supplemental New Drug Application (sNDA) for dolutegravir 10mg and 25mg oral tablets, reducing the weight limit from at least 40kg to at least 30kg, in ages 6 to less...

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