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RedHill Biopharma Announces Approval for Talicia®
Tuesday, September 19, 2023RedHill Biopharma has received approval from the US Food and Drug Administration FDA for a change in the dosing regimen of its drug Talicia used for the eradication of H pylori infection
Agilent Technologies and National Cancer Centre Singapore Enter into Research Collaboration Agreement
Tuesday, September 19, 2023Agilent Technologies signed a research collaboration agreement with the National Cancer Centre Singapore NCCS to accelerate a step forward in the field of translational cancer research particularly in the context of Asianprevalent cancers
AstraZeneca and Daiichi Sankyo Recommend for Approval of Enhertu
Saturday, September 16, 2023Enhertu developed jointly by AstraZeneca and Daiichi Sankyo has received a recommendation for approval in the European Union EU as a monotherapy for the treatment of adult patients with advanced nonsmall cell lung cancer NSCLC
Dizal's Golidocitinib New Drug Application Accepted in China
Friday, September 15, 2023Dizal has announced that the Centre for Drug Evaluation CDE of the China National Medical Products Administration NMPA has accepted the New Drug Application NDA for golidocitinib for the treatment of relapsed or refractory peripheral Tcell lymphoma r...
MGI Tech Partners with National Cancer Centre Singapore
Friday, September 15, 2023MGI Tech has entered into research partnership with the National Cancer Centre Singapore NCCS to advance the understanding of Asianprevalent cancers through comprehensive genomic profiling
Oscotec and ADEL Receive FDA Clearance for ADEL-Y01
Friday, September 15, 2023Oscotec and ADEL have jointly received clearance from the US Food and Drug Administration FDA to proceed with their investigational new drug IND application for ADELY which is intended for the treatment of Alzheimers disease AD
Takeda Pharmaceuticals Announces FDA Acceptance of Biologics Licence Application for ENTYVIO®
Thursday, September 14, 2023Takeda Pharmaceuticals announced that the US Food and Drug Administration FDA has accepted its Biologics Licence Application BLA for the subcutaneous SC administration of ENTYVIO vedolizumab as a maintenance therapy for adults with moderately to seve...
Pharmazz and Sun Pharmaceutical Industries Enter into Agreement
Thursday, September 14, 2023Under the terms of the agreement Sun Pharma has been granted the rights to market Sovateltide in India utilising the brand name Tyvalzi Sovateltide In return Pharmazz will receive upfront and milestone payments including royalties
Entera Bio Announces Collaboration with OPKO Biologics
Wednesday, September 13, 2023Entera Bio and OPKO Biologics have joined forces in a research collaboration to advance the development of oral peptide tablet formulations designed to address obesity and intestinal malabsorption syndromes
Shanghai Henlius Biotech Expands Collaboration with KGbio Genexine Biologics
Wednesday, September 13, 2023Shanghai Henlius Biotech has entered into an exclusive licencing agreement with PT Kalbe Genexine Biologics KGbio for the development and commercialisation of HANSIZHUANG a serplulimab injection targeting two indications including extensivestage smal...
