
Roche will gain exclusive worldwide rights to develop, manufacture, and commercialize Ionis’ investigational RNA-based therapeutic candidates for Alzheimer's and Huntington's disease.
Roche will gain exclusive worldwide rights to develop, manufacture, and commercialize Ionis’ investigational RNA-based therapeutic candidates for Alzheimer's and Huntington's disease.
The program will improve access to adeno-associated virus gene therapy vectors.
New routes to cancer treatment can be found with the help of tumor-infiltrating lymphocyte (TIL) therapies.
Orakl Oncology has raised funds to develop its precision oncology platform and accelerate drug development.
Eli Lilly and Company has received a complete response letter from FDA for its anti-dermatitis biologic therapeutic, lebrikizumab.
The program will allow sponsors of certain CBER and/or CDER-regulated products more frequent communication with FDA staff.
The prize was awarded jointly to Katalin Karikó and Drew Weissman for their groundbreaking discovery regarding modification of the bases in mRNA.
Pfizer has entered into a collaboration with Ginkgo Bioworks to discover novel RNA molecules across priority research areas.
Government provides a spoonful of sugar, and genuine leadership, for good medicines.
Biologics formulation comes with a unique set of challenges, which can be overcome through innovative strategies and good partnerships.
Webinar Date/Time: Tue, Oct 17, 2023 10:00 AM EDT
Tumour-infiltrating lymphocyte (TIL) therapies offer a new route to target cancer.
Maik Jornitz, Principal Consultant, BioProcess Resources LLC, discusses the definition of patient safety and how to implement new technologies into upgraded facilities.
The EMA’s Committee for Medicinal Products for Human Use has given a positive opinion on Sandoz’ biosimilar trastuzumab for breast and gastric cancer.
Despite its success, clinical and logistical roadblocks to mRNA cancer vaccine development remain.
Recipharm will provide analytical and process development capabilities to support toxicology studies, in addition to GLP manufacturing of lipid nanoparticles to capture the active pharmaceutical ingredient, an antigen peptide.
The agreement states that Orbit will implement its bead-based peptide display engine to discover peptide leads specific to targets related to specific tumors.
Nanoparticles offer the potential for a safer, more effective method of drug delivery to the patient.
Image analysis algorithms coupled with microscopy techniques can be used to characterize aggregates of therapeutic proteins.
Innovations in downstream processing accelerate development, enhance efficiency, and promote sustainability.
Pharma's ability to continually reinvent itself will be critical in growing future business operations.
Extensive research on various gene editing techniques could inform the future of mRNA therapies.
FDA has halted enrollment in clinical studies for Gilead Sciences’ magrolimab, a biologic treatment in development for acute myeloid leukemia.
With this agreement, Chiesi Global Rare Diseases will co-develop drug delivery systems with Aliada Therapeutics for large molecule therapeutics that can cross the blood-brain barrier.
A major grant from the Bill & Melinda Gates Foundation will bolster efforts to fight the global HIV/AIDS epidemic.