Drugs

News and Updates about the regulations in Drugs and Pharma

Pharmanovia and Lindis Biotech Join Forces to Market Catumaxomab for Treating Malignant Ascites

Pharmanovia, an international pharmaceutical company specializing in novel and revitalized medicines, has augmented its oncology offerings through a licensing agreement for catumaxomab, aimed at treating malignant ascites. With this arrangement, Pharmanovia gains exclusive rights to introduce catumaxomab, a pioneering bi-specific

Pharmanovia and Lindis Biotech Join Forces to Market Catumaxomab for Treating Malignant Ascites Read More »

Tagomics Ltd. Partners with Agilent Technologies for Joint Co-Marketing Initiative in Multiomic Profiling

Tagomics Ltd., known for its groundbreaking work in biomarker discovery and diagnostics, has announced a strategic partnership with Agilent Technologies, a key player in genomic tools, to embark on a co-marketing initiative. This collaboration will enable selected clients to access

Tagomics Ltd. Partners with Agilent Technologies for Joint Co-Marketing Initiative in Multiomic Profiling Read More »

Abbott Introduces New Strategies and Collaborations to Boost Diversity in Clinical Trials

Abbott, in the third year marking its substantial Diversity in Clinical Trials campaign, has introduced ‘Advancing Diversity in Clinical Trials,’ a publication offering strategies to enhance diversity within clinical research teams throughout the United States. At the same time, Abbott

Abbott Introduces New Strategies and Collaborations to Boost Diversity in Clinical Trials Read More »

Samsung Biologics Secures Manufacturing Agreements of $668 Million with a European Pharma Firm

Samsung Biologics, a renowned contract development and manufacturing organization (CDMO), has recently forged a series of manufacturing agreements with a pharmaceutical company based in Europe. These newly revealed contracts, valued at over $668 million in total, are set to extend

Samsung Biologics Secures Manufacturing Agreements of $668 Million with a European Pharma Firm Read More »

Merck’s Phase 3 Study Reveals Successful Outcomes for Subcutaneous Pembrolizumab with Berahyaluronidase Alfa

Merck, recognized as MSD outside the United States and Canada, has announced encouraging topline outcomes from the pivotal phase 3 MK-3475A-D77 study. This investigation is analyzing whether the subcutaneous delivery of pembrolizumab—a renowned anti-PD-1 therapy by Merck, commercially known as

Merck’s Phase 3 Study Reveals Successful Outcomes for Subcutaneous Pembrolizumab with Berahyaluronidase Alfa Read More »