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Accurately targeted immunotherapies through reliable neoantigen recognition enable personalized medicine development.
Activation and expansion are essential for success in both autologous and allogeneic therapies.
Continuous manufacturing and a quality-by-design development approach are a natural fit.
December 06, 2021
Recordati’s blockbuster acquisition of EUSA Pharma gives them access to a portfolio of four drugs that treat rare cancers.
December 03, 2021
Fujifilm’s center adds local support in Suzhou, China for cell culture media optimization.
This collaboration aims to better understand Alzheimer’s and Parkinson’s disease and increase drug discovery and development success rates.
High price tags threaten to block patient access to potentially life-saving cures and treatments.
Increased patient-centricity and alternative dosage forms require careful consideration when selecting the best taste-masking approach.
Polymeric amorphous solid dispersions are the most commonly used technology, but amorphous APIs remain inherently unstable.
December 02, 2021
EMA has fully validated the marketing authorization application for Atara Biotherapeutics’ off-the-shelf allogeneic T-cell therapy, tab-cel (tabelecleucel), with an approval decision expected in 2022.
Particle analysis is a critical component of pharmaceutical development, providing assurances of the quality and performance of the final dosage form.
Chinook Therapeutics has formed a 50/50 joint venture with investors to develop kidney disease therapies in China.
November 30, 2021
Researchers from MIT have developed novel nanosensors for the detection of the nucleocapsid and spike protein of the SARS-CoV-2 virus.