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Sosei Provides an Update on Its Immuno-Oncology Clinical Program with AstraZeneca
Sosei Group Corporation announces that its immuno-oncology collaboration with AstraZeneca is progressing well. The first patient has been dosed in an expansion cohort in the Phase 1b…
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Selvita appoints Steffen Heeger as Chief Medical Officer
Selvita S.A. (WSE:SLV), a clinical stage drug discovery and development company focused on innovative medicines for oncology patients and drug discovery services, announced the…
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Major research project launched to crack aspirin’s anti-cancer properties
Cancer Research UK launches an international study to answer the final questions before aspirin could be recommended to reduce cancer risk.
Studies have estimated that widespread…
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EMA accepts Teva’s Fremanezumab Marketing Authorization Application
Teva Pharmaceutical announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA) for fremanezumab, an anti-calcitonin gene-related…
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Cobra Biologics and Symbiosis clinched $2.5m USD collaborative grant
International contract development and manufacturing organisation (CDMO) of biologics and pharmaceuticals, Cobra Biologics and Symbiosis Pharmaceutical Services asserted having clinched…
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Anika Therapeutics collaborates with IIB to develop MSC therapy for Osteoarthritis
Anika Therapeutics integrated orthopedic medicines company based on its proprietary hyaluronic acid ("HA") technology, today announced an agreement with the Institute of Integrative…
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Syndax Pharmaceuticals affirms Oncology Clinical Trial venture with AstraZeneca
Clinical stage biopharmaceutical company developing an innovative pipeline of cancer therapies, Syndax Pharmaceuticals ventured into new Clinical collaboration with AstraZeneca to…
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China’s Transcatheter MitralStitch mitral valve repair system completed
Yunnan Fuwai Hospital declares successful completion of clinical case of MitralStitch mitral valve repair system. The operation was jointly conducted by the team of Professor Pan…
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Ambry Genetics partners Invicro to extend customized genomics and imaging services
Ambry Genetics and Invicro partner to offer customized genomics and imaging services for the pharmaceutical and biotechnology industry, exhibiting profound emphasis on Oncology and…
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NuvOx Pharma concedes FDA’s approval to Phase II Clinical Trial
FDA permits a Phase II Clinical Trial in 60 stroke patients, NuvOx Pharma announced FDA approval to proceed to test its investigational drug product, dodecafluoropentane emulsion…
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Ceterix Orthopedics finishes enrollment in STITCH for horizontal meniscus tears
Developer of novel surgical tools to enhance a surgeon's ability to perform minimally invasive orthopedic procedures, Ceterix Orthopedics declared completion of enrollment in STITCH…
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Puma Biotechnology declares results of Phase II ‘basket’ Clinical Trial
Phase II ‘basket’ clinical trial of PB272 (neratinib) in patients with tumors harboring HER2 or HER3 mutations results were declared by Puma Biotechnology as published in the journal…
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SkylineDx collaborates with Mayo Clinic to curate Diagnostic tests for Melanoma
SkylineDX affirmed foraying into a strategic collaboration to curate novel diagnostic tests to enhance clinical decision making for melanoma patients. The Joint development agreement…
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Novartis declares results of ELIANA Clinical Trial of kymriah
Novartis declared results from ELIANA Clinical Trial of kymriah in refractory pediatric and young adult patients with B-cell acute lymphoblastic leukemia. Kymriah claimed to become one…
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Upsher-Smith sought FDA approval for Bumetanide Tablets
Upsher-Smith Laboratories, LLC declared that it sought U.S Food and Drug Administration's approval for new drug application (ANDA) for Bumetanide Tablets, USP, 0.5 mg, 1 mg, and 2 mg,…
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MedShape declares successful performance of first surgeries using DynaNail XL
Industry leader in orthopaedic devices using advanced functional materials, MedShape declared successful performance of first surgeries using DynaNail XL TTC Fusion System. The…
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Mallinckrodt enrolls first patient in Phase 4 Trial of H.P Acthar Gel
Mallinckrodt plc affirmed enrolling first patient in the company's Phase 4, multi center, randomized, double-blind, placebo-controlled pilot study to facilitate evaluation of the…
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U.S FDA grants Fast Track designation to Takeda’s TAK-426
Takeda Pharmaceutical company Limited asserted that the U.S Food and Drug Administration has extended Fast Track designation to TAK-426 i.e Takeda's Zika virus vaccine candidate. …
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CutisPharma confirms FDA’s sanction of FIRVANQ for Clostridium difficile
U.S FDA has sanctioned CutisPharma's FIRVANQ (vancomycin hydrochloride) for oral solution, for the treatment of Clostridium difficile associated diarrhea and enterocolitis caused by …
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FDA extends 510(K) clearance for electroCore’s gammaCore (nVNS)
electroCore sought 510(k) clearance from the U.S Food and Drug Administration for an extended label for gammaCore (nVNS) as an acute treatment of pain associated with migraine in adult…
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