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Study claims the Importance of familiarizing the risks and benefits of phase 1 trials in pediatric cancer

On average, 1 in 10 children who enroll in pediatric phase I cancer trials are improved after the trial, and 1 in 50 die from drug-related complications, according to a new systematic review and meta-analysis published this week in...

FDA Approval for Allegraโ€™s filing for supplemental new drug application LILETTAยฎ

Allergan plc, a leading global pharmaceutical company, and Medicines360, a global nonprofit women's health pharmaceutical company with a mission of expanding access to quality medicines, today announced that the U.S. FDA has accepted for filing Medicines360's supplemental New Drug...

AbbVie and Voyager Therapeutics collaborates for Neurodegenerative Diseases

AbbVie , a global biopharmaceutical company, and Voyager Therapeutics, Inc. , a clinical-stage gene therapy company announced that they have entered into an exclusive strategic collaboration and option agreement to develop and commercialize vectorized antibodies directed against tau for...

Astrazenecaโ€™s Imfinzi for unresectable Stage III non-small cell lung cancer gets FDA approval

AstraZeneca and MedImmune, its global biologics research and development arm, today announced that the US FDA has approved Imfinzi for the treatment of patients with unresectable Stage III non-small cell lung cancer (NSCLC) whose disease has not progressed following...

Allergan Presents Data at the 2018 American Academy of Dermatology (AAD) Annual Meeting in San Diego

The meeting will be held at the San Diego Convention Center and the scheduled times (noted in local Pacific Time) for the Allergan presentations, titles and authors are as follows: Podium PresentationsOnce-Daily Oral Sarecycline 1.5 mg/kg/day...

Amgen sets up a FDA Advisory Committee Meeting To Review Potential New Use Of BLINCYTO

Amgen announced that the Oncologic Drugs Advisory Committee of the U.S. FDA will review data supporting the BLINCYTOยฎ (blinatumomab) supplemental Biologics License Application (sBLA) for the treatment of patients with minimal residual disease (MRD)-positive B-cell precursor acute lymphoblastic leukemia...

AbbVie presents New, Late Breaking Investigational Data at 2018 at AAD Annual meeting

AbbVieย  a global research and development-based biopharmaceutical company, today announced it will present new, late-breaking data across investigational medicines and HUMIRAยฎ (adalimumab) at the 2018 American Academy of Dermatology (AAD) Annual Meeting (February 16-20, San Diego). ...

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