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Novartis to divest the Sandoz US dermatology business and generic US oral solids portfolio to…
Novartis announced it has agreed to sell selected portions of its Sandoz US portfolio, specifically the Sandoz US dermatology business and generic US oral solids portfolio, to Aurobindo…
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Tetraphase Announces FDA Approval of XERAVA (Eravacycline) for cIAI
Tetraphase Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has granted approval of XERAVA (eravacycline) for the treatment of complicated intra-abdominal…
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PCI Expands Cold Chain Infrastructure with Dedicated -40°C Facility
PCI announced the completion of a purpose built -40°C storage and distribution facility at our North American Clinical Services Center of Excellence.
The site, located in Rockford,…
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FDA Approves Merck’s two new HIV-1 medicines DELSTRIGO and PIFELTRO
Merck announced that the U.S. Food and Drug Administration (FDA) has approved two new HIV-1 medicines: DELSTRIGO, a once-daily fixed-dose combination tablet of doravirine (100 mg),…
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Novartis receives EC approval of its CAR-T cell therapy, Kymriah (tisagenlecleucel)
Novartis announced that the European Commission (EC) has approved Kymriah (tisagenlecleucel, formerly CTL019). The approved indications are for the treatment of pediatric and young…
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Tolero Announces Clinical Research Collaboration with AbbVie for Acute Myeloid Leukemia Trial
Tolero Pharmaceuticals has entered into a clinical research collaboration with AbbVie, a research-based global biopharmaceutical company, exploring the potential of combination therapy…
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CNDA grants rapid approval of Roche’s Alecensa (alectinib) as a treatment for ALK-positive lung…
Roche announced that the China National Drug Administration (CNDA) has granted marketing authorisation for Alecensa (alectinib) as a monotherapy treatment for patients with anaplastic…
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Eisai And Merck Announce FDA Approval Of LENVIMA Capsules For Treatment Of Unresectable HCC
Eisai Inc. and Merck, known as MSD outside of the United States and Canada, announced today that the U.S. Food and Drug Administration (FDA) approved the kinase inhibitor LENVIMA …
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BioNTech Signs Collaboration Agreement with Pfizer to Develop mRNA-based Vaccines for Prevention of…
BioNTech AG announced that it has entered into a multi-year research and development (R&D) collaboration with Pfizer Inc. to develop mRNA-based vaccines for prevention of influenza…
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NIH-funded researchers reverse congenital blindness in mice
Researchers funded by the National Eye Institute (NEI) have reversed congenital blindness in mice by changing supportive cells in the retina called Müller glia into rod photoreceptors.…
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Janssen Reports Positive Topline Results for ATLAS Phase III Study of a Novel, Long Acting…
The Janssen Pharmaceutical Companies of Johnson & Johnson confirmed positive topline results from the global, Phase III Antiretroviral Therapy as Long-Acting Suppression (ATLAS)…
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Almac Discovery, Elasmogen and Innovate UK Collaborate to Develop VNAR Based Oncology Platform
Almac Discovery, a biopharmaceutical company focused on discovering and identifying innovative therapeutics for the treatment of cancer, and Elasmogen, an SME focused on the development…
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Solid Tumors Targeted in New CAR T-Cell Immunotherapy Trial
Seattle Children’s has opened a chimeric antigen receptor (CAR) T-cell immunotherapy trial for children and young adults with relapsed or refractory non-central nervous system…
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Ambys Medicines and Takeda Announce Partnership to Pioneer First-in-Class Therapies for the…
Ambys Medicines and Takeda Pharmaceutical Company Limited announced that they have entered into a partnership to support the advancement of the Ambys platform and pipeline.
“We are…
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Amgen Breaks Ground On Next-Generation Biomanufacturing Plant In Rhode Island
Amgen announced the groundbreaking of its new next-generation biomanufacturing plant that will be constructed at its West Greenwich, R.I. campus. The new plant is the first-of-its-kind…
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PRIME designation granted by EMA for RG6042 for treatment of Huntington’s disease
Roche announced that the European Medicines Agency (EMA) has granted PRIME (PRIority MEdicines) designation for the company’s investigational medicine RG6042 (formerly known as…
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Novartis marks a new era for migraine patients with the EU approval of Aimovig
Novartis announced that the European Commission (EC) approved Aimovig (erenumab) for the prevention of migraine in adults experiencing four or more migraine days per month. Aimovig is…
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Selumetinib granted orphan designation in Europe for neurofibromatosis type 1
AstraZeneca and Merck & Co., Inc., Kenilworth, NJ, US (known as MSD outside the US and Canada) announced that the European Medicines Agency (EMA) has granted orphan designation to…
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LEO Pharma to Expand Its Lead in Medical Dermatology with Acquisition of Bayer’s Prescription…
LEO Pharma and Bayer announced that LEO Pharma has entered into a definitive agreement to buy Bayer’s global prescription dermatology unit. The portfolio to be acquired includes branded…
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MilliporeSigma and InnoCore Pharmaceuticals to Improve Patient Compliance with New Drug Delivery…
MilliporeSigma and InnoCore Pharmaceuticals; Groningen, Netherlands, have entered into a global cooperation agreement to provide InnoCore’s proprietary SynBiosys biodegradable polymer…
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