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Daiichi Sankyo Announces Decision to Develop Vaccine in Japan for Novel Corona Virus Infection…
Daiichi Sankyo Company, Limited announced its decision to develop a genetic (mRNA) vaccine for the novel corona virus infection (hereinafter, COVID-19) in Japan.
In April, 2020,…
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Sofinnova Partners Announces Sale of Corvidia Therapeutics to Novo Nordisk
Sofinnova Partners, a leading European life sciences venture capital firm based in Paris, London and Milan, announced the sale of its portfolio company Corvidia Therapeutics to Novo…
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Grifols starts production of its hyperimmune immunoglobulin as a potential passive immune therapy…
Grifols announced the start of production of its anti-SARS-CoV-2 hyperimmune immunoglobulin with specific antibodies using the plasma of people who have overcome the disease. It is the…
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European Commission approves Sarclisa for adults with relapsed and refractory multiple myeloma
The European Commission (EC) has approved Sarclisa (isatuximab) in combination with pomalidomide and dexamethasone (pom-dex) for the treatment of adult patients with relapsed and…
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AbbVie and Jacobio Announce Strategic Collaboration to Advance SHP2 Inhibitors
AbbVie and Jacobio Pharmaceuticals announced a global, strategic collaboration to develop and commercialize SHP2 inhibitors, which target a key node in cancer and immune cells.
SHP2 …
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Roche initiates phase III clinical trial of Actemra/RoActemra plus remdesivir in hospitalised…
Roche announced the initiation of a global phase III, randomised, double-blind, multicentre study (REMDACTA) to evaluate the safety and efficacy of Actemra/RoActemra plus the…
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Almac Group Supports Two COVID-19 Clinical Studies in Sub-Saharan Africa
Almac Group has received a $288,000 grant to support a clinical study in Sub-Saharan Africa in efforts to find a treatment for Coronavirus. This was awarded from the COVID-19…
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FDA grants priority review of Nucala for patients with Hypereosinophilic Syndrome (HES)
GlaxoSmithKline plc (GSK) announced that the US Food and Drug Administration (FDA) has granted a priority review for the company’s application seeking approval of Nucala (mepolizumab)…
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Boehringer Acquires Northern Biologics’ Preclinical Cancer Antibody Pipeline
Boehringer Ingelheim announced the acquisition of Northern Biologics Inc., a wholly owned subsidiary of Northern LP. By acquiring this entity, which focuses on therapeutic antibodies…
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Sorrento And Mount Sinai To Jointly Develop COVI-SHIELD Antibody Therapy Targeting SARS-CoV-2…
Sorrento Therapeutics, Inc. and Mount Sinai Health System have agreed to join forces in the investigation and development of an antibody cocktail (COVI-SHIELD) to potentially treat…
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Schreiner MediPharm Supplies Booklet-Label for Clinical Trial at Sanofi
Schreiner MediPharm has developed a compact Booklet-Label for a needle protection system used in an international phase III clinical trial conducted by pharmaceutical corporation…
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AstraZeneca and Oxford University announce landmark agreement for COVID-19 vaccine
AstraZeneca and the University of Oxford announced an agreement for the global development and distribution of the University’s potential recombinant adenovirus vaccine aimed at…
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Novartis announces plan to initiate clinical trial of canakinumab for patients with COVID-19…
Novartis announced plans to initiate a Phase III clinical trial to study canakinumab in patients with COVID-19 pneumonia. The CAN-COVID trial will examine the efficacy of utilizing…
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Gilead Announces Results From Phase 3 Trial of Investigational Antiviral Remdesivir in Patients With…
Gilead Sciences, Inc. announced topline results from the open-label, Phase 3 SIMPLE trial evaluating 5-day and 10-day dosing durations of the investigational antiviral remdesivir in…
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Griffith University researchers on the road to COVID-19 vaccine
Griffith University researchers have joined forces with scientists from Indian Immunologicals Limited (IIL), a leading vaccines manufacturing company based in Hyderabad, India to…
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Novartis Kymriah receives FDA Regenerative Medicine Advanced Therapy designation in follicular…
Novartis announced that the US Food and Drug Administration (FDA) granted Regenerative Medicine Advanced Therapy (RMAT) designation to Kymriah (tisagenlecleucel), for an investigational…
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Gilead, Kite and oNKo-innate Announce Research Collaboration to Discover Cancer Immunotherapies…
Gilead Sciences, Inc. Kite, a Gilead Company, and oNKo-innate announced the companies have entered into a three-year cancer immunotherapy research collaboration to support discovery and…
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Intensity Therapeutics Signs Clinical Collaboration Agreement with BMS for Advanced Solid Tumors
Intensity Therapeutics announced it has entered into a clinical trial collaboration agreement with Bristol Myers Squibb Company. The program will evaluate the safety and efficacy of…
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FDA Approves First Therapy for Children with Debilitating and Disfiguring Rare Disease
The U.S. Food and Drug Administration approved Koselugo (selumetinib) for the treatment of pediatric patients, 2 years of age and older, with neurofibromatosis type 1 (NF1), a genetic…
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Acceleron Receives FDA Breakthrough Therapy Designation for Sotatercept in Pulmonary Arterial…
Acceleron Pharma Inc. announced that the United States Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to sotatercept for the treatment of patients with…
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