Regeneron’s Veopoz scores FDA approval for rare immune disease
The monoclonal antibody is the first to be approved for both adult and paediatric patients with CHAPLE disease.
22 August 2023
22 August 2023
The monoclonal antibody is the first to be approved for both adult and paediatric patients with CHAPLE disease.
The company’s generative and predictive AI-powered drug discovery platform is already being used by Eli Lilly.
The company will bolster its medical dermatology pipeline by gaining rights to Timber’s TMB-001.
The vaccine is administered to pregnant people to prevent RSV-related lower respiratory tract disease and severe LRTD in infants.
The company's supplier intelligence suite offers supplier compliance level statistics and audit data to pharma firms.
The Phase III trial for the Cabometyx and Tecentriq combination treatment met progression-free survival endpoint in metastatic prostate cancer.
The FDA granted Calliditas a December 2023 priority review date for its IgA nephropathy drug Tarpeyo, which already has an accelerated approval.
Outsourcing in Clinical Trials Southern California Conference 2023 will be returning to Hyatt Regency La Jolla at Aventine, USA on the 26th-27th September 2023! Focusing on interactive discussions to provide insight into the current major operational issues with running clinical trials in the coming years.
The success of CAR-Ts in MM has fueled R&D investment into this class of therapy, with more CAR-Ts in development than all other cell and gene therapy classes combined. The approval of the autologous CAR-T cell therapies Abecma and Carvykti sees the CAR-T pipeline mostly constituted of autologous drugs. However, there are also multiple allogeneic CAR-Ts in the pipeline, with these therapies having an “off-the-shelf” advantage over autologous therapies.
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