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Clinical Catch-up from Last Week: May 5-10
biospace
May 13, 2019
Almost every week, biopharma companies release results from ongoing clinical trials. Here’s a roundup of some of the top clinical trial news from the previous week.
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Blood samples to help choose early phase clinical trials for cancer patients
pharmatimes
April 28, 2019
Cancer Research UK has published research that could help match cancer patients with no other treatment options to clinical trials with experimental medicines.
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Biosimilars that have entered Phase III clinical trials
PharmaSources/Caicai
April 23, 2019
Biosimilars that have entered Phase III clinical trials
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NIH initiates first clinical trial of universal influenza vaccine
pharmaceutical-technology
April 09, 2019
NIH initiates first clinical trial of universal influenza vaccine
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LY09004 Approved for Clinical Trials in China, Luye Pharma Steps-up Global R&D Investment in Biopharma Medicines
firstwordpharma
April 04, 2019
Luye Pharma announced that the company has received approval from the National Medical Products Administration of China ……
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BREAKING NEWS Myoderm Announces Leadership Transition
contractpharma
April 04, 2019
CEO Michael Cohen to become Executive Chairman; COO James Lovett to be promoted to CEO
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LabConnect Appoints Medical Director
contractpharma
March 28, 2019
Dr. Anthony Todd Everhart brings over a decade of experience to the company
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SourcingLink.net Enters into an Exclusive Worldwide Licensing Agreement with NanoSmart Pharmaceuticals
pharmafocusasia
March 27, 2019
SourcingLink.net, Inc. (SNET), announced today that it entered into an exclusive worldwide licensing agreement with NanoSmart Pharmaceuticals, Inc. for the right to use NanoSmart’s nanoparticle platform technologies to develop and...
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GT Biopharma Restructures Management Team
contractpharma
March 27, 2019
Cataldo named chief executive officer, Weldon appointed as chief financial officer.
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Indian Government notifies new rules for drugs and clinical trials
expressbpd
March 26, 2019
The new rules reduce the time for approving applications to 30 days for drugs manufactured in India and 90 days for those developed outside the country.