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MS Pharma Announces Acquisition of Genepharm
MS Pharma, a fast growing pharmaceutical company based in Jordanand operating across the Middle East, Turkey and Africa, announced that it has entered into an agreement to acquire 100%…
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Gilead and insitro Announce Strategic Collaboration to Discover and Develop Novel Therapies for NASH
Gilead Sciences Inc. and insitro announced today that the companies have entered into a strategic collaboration to discover and develop therapies for patients with nonalcoholic…
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Lynparza approved in EU for the treatment of germline BRCA-mutated HER2-negative advanced breast…
AstraZeneca and MSD Inc., Kenilworth, N.J., US (MSD: known as Merck & Co., Inc. inside the US and Canada) announced the European Commission has approved Lynparza (olaparib) as a…
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WuXi Biologics and NBE-Therapeutics Announce Comprehensive ADC Development and Manufacturing…
WuXi Biologics, a leading global open-access biologics technology platform company offering end-to-end solutions for biologics discovery, development and manufacturing, and…
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Concerto HealthAI Enters Precision Oncology Collaboration with Pfizer
Concerto HealthAI announced that they have entered into a collaboration with Pfizer to advance work in Precision Oncology using Concerto HealthAI’s eurekaHealthTM platform, artificial…
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Regeneron and Alnylam Announce Broad Collaboration to Discover, Develop and Commercialize RNAi…
Regeneron Pharmaceuticals and Alnylam Pharmaceuticals announced a collaboration to discover, develop and commercialize new RNA interference (RNAi) therapeutics for a broad range of…
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NIH begins first-in-human trial of a universal influenza vaccine candidate
The first clinical trial of an innovative universal influenza vaccine candidate is examining the vaccine’s safety and tolerability as well as its ability to induce an immune response in…
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Sandoz resubmits biosimilar pegfilgrastim application to US FDA
Sandoz, a Novartis division and a global leader in biosimilars, today resubmission of its Biologics License Application (BLA) for a proposed biosimilar pegfilgrastim to the US Food and…
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Novartis receives FDA approval for Mayzent (siponimod), the first oral drug to treat secondary…
Novartis announced that the US Food and Drug Administration (FDA) has approved Mayzent (siponimod) for the treatment of adults with relapsing forms of multiple sclerosis, including…
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MilliporeSigma Opens First M Lab Collaboration Center in Europe
MilliporeSigma officially opened its new M Lab Collaboration Center in Molsheim, France. The center is MilliporeSigma's first in Europe and ninth worldwide, providing biopharmaceutical…
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Merck To Collaborate with GenScript to Accelerate Cell and Gene Therapy Industrialization in China
Merck announced the signing of a non-binding Memorandum of Understanding with Chinese biotech company GenScript for a strategic alliance focusing on plasmid and viral vector…
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FDA approves Roche’s Tecentriq in combination with chemotherapy for the initial treatment of adults…
Roche announced that the U.S. Food and Drug Administration (FDA) approved Tecentriq (atezolizumab), in combination with carboplatin and etoposide (chemotherapy), for the initial…
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Data from GARNET study indicates robust activity of dostarlimab in patients with advanced or…
TESARO, an oncology-focused business acquired by GlaxoSmithKline plc, announced the presentation of data from the Phase 1/2 GARNET study evaluating dostarlimab in women with recurrent…
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Boehringer Ingelheim announces FDA and EMA regulatory submission for nintedanib in systemic…
Boehringer Ingelheim has filed for regulatory approval of nintedanib in patients with systemic sclerosis associated interstitial lung disease (SSc-ILD) with the FDA and EMA. Nintedanib…
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Iktos Announces Collaboration with Merck for Use of Iktos AI Technology across Three Drug Discovery…
Iktos announced a collaboration agreement with Merck KGaA, Darmstadt, Germany where Iktos generative modelling artificial intelligence (AI) technology will be used to facilitate the…
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Existing drug found to dampen chemo side effects in breast cancer — in a dish
Patients with HER2-positive breast cancer face something of a predicament: The most effective drug to treat the cancer is also the most toxic.
Trastuzumab, sold under the brand name…
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European Commission approves Roche’s MabThera (rituximab) for a rare autoimmune disease
Roche announced that the European Commission has approved MabThera® (rituximab) for the treatment of adults with moderate to severe pemphigus vulgaris (PV), a rare condition…
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EC approves Roche’s Hemlibra for people with severe haemophilia A without factor VIII inhibitors
Roche announced that the European Commission has approved Hemlibra (emicizumab) for routine prophylaxis of bleeding episodes in people with severe haemophilia A (congenital factor VIII…
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Seres Therapeutics Announces Microbiome Immuno-Oncology Focused Collaboration with AstraZeneca
Seres Therapeutics announced a three-year research collaboration with AstraZeneca. The collaboration will focus on advancing mechanistic understanding of the microbiome in augmenting…
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FDA Approves Pfizer’s Oncology Biosimilar TRAZIMERA (trastuzumab-qyyp), a Biosimilar to Herceptin 1
Pfizer Inc. announced the United States (U.S.) Food and Drug Administration (FDA) has approved TRAZIMERA (trastuzumab-qyyp), a biosimilar to Herceptin (trastuzumab), for the treatment…
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