Innovus Pharmaceuticals and Elis Pharmaceuticals have finalized a second exclusive license and distribution agreement for Zestra. Read More »

Roche's VENTANA ALK (D5F3) CDx Assay has received approval from the U.S. Food and Drug Administration to be used in conjunction with the VENTANA BenchMark ULTRA automated slide stainer. Read More »

Bayer has submitted its supplemental New Drug Application for Stivarga tablets to the U.S. Food and Drug Administration. Read More »

Jordan Howard, the leading rusher for the Chicago Bears, attended the 2016 Pulmonary Fibrosis Foundation’s volunteer meeting where he dedicated himself to fighting pulmonary fibrosis. Read More »

The U.S. Food and Drug Administration has approved Propeller Health's platform for use with GSK’s Ellipta inhaler. Read More »

The National Pharmaceutical Council Board of Directors has appointed Dr. Joshua Ofman as its new vice chairman. Read More »

AbbVie's oral poly polymerase inhibitor valiparib has been granted Orphan Drug Designation by the U.S. Food and Drug Administration. Read More »

Kedrion Biopharma and Kamada's Biologics License Application for human anti-rabies immunoglobulin therapy has been accepted for review by the U.S. Food and Drug Administration. Read More »

Eli Lilly and Co.'s analysis of its Phase 3 baricitinib trial efficiency and safety data, as well as that of other Phase 2 trials, will be presented at the American College of Rheumatology/Association of Rheumatology Health Professionals Annual Meeting, which is being held on Nov. 11-16 in Washington, D.C. Read More »

HalioDx SAS has released a report detailing the progress being made by its clinical research services. Read More »

URAC has accredited CVS Caremark's Pharmacy Adviser counseling program run by the Health Call Center and its Pharmacy Benefit Management and Drug Therapy Management. Read More »

ACADIA Pharmaceuticals' ENHANCE-1 Phase III trial involving pimavanserin has been initiated to assess the ability of pimavanserin to treat schizophrenia in patients who have had a negative response to the antipsychotic therapies currently in use. Read More »

Anthera Pharmaceuticals' Phase 2 BRIGHT-SC trial data has been selected as a poster presentation at the 2016 American Society of Nephrology’s Kidney Week Annual Meeting. Read More »

Momenta Pharmaceuticals and Mylan N.V.'s first patient in its Phase 1 study of M834 has been dosed. The trial will evaluate M834's pharmacokinetics, safety and immunogenicity. Read More »

Ajanta Pharma USA, subsidiary of Ajana Pharma Ltd., India, has released Amlodipine + Olmesartan Medoxomil Tablets in the United States. Read More »

Merck KGaA will present the data on its investigational drug for the treatment of systemic lupus erythematosus ataciept at the 2016 American College of Rheumatology/Association of Rheumatology Health Professionals Annual Meeting. Read More »

Aralez Pharmaceuticals Trading DAC has finalized the purchase of the rights to Toprol-XL in the U.S. and Authorized Generic from AstraZeneca. Read More »

Amgen's results of its Phase 3 coronary intravascular imaging trial, call GLAGOV, will be presented at the American Heart Association Scientific Sessions 2016. Read More »

ACADIA Pharmaceuticals' Phase II SERENE trial involving pimavanserin has begun. Read More »

The Female Health Co.'s transformational merger with Aspen Park Pharmaceuticals has been finalized with both sides agreeing to modified terms. Read More »