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Candel Therapeutics reports major success in prostate cancer trial, aiming for FDA approval by end of 2026.
Candel Therapeutics reported positive phase 3 trial results for CAN-2409 in treating localized prostate cancer, showing a 30% improvement in disease-free survival.
The company received FDA RMAT designation for prostate cancer and orphan designation for pancreatic cancer from the EMA.
Candel plans to submit a BLA by Q4 2026 and has sufficient funds to operate until Q1 2027.
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Candel Therapeutics informa un gran éxito en el ensayo de cáncer de próstata, con el objetivo de obtener la aprobación de la FDA para finales de 2026.