Selecting TYK2 inhibitors can reduce the inhibition of other immune-related pathways in the body, reduce the risk of infection, and be safer in clinical practice.
PAES, as mandated by EU Commission Delegated Regulation No 357/2014, refers to an efficacy study required by a Competent Authority under any of the specified conditions outlined in the regulation.
Mission Therapeutics reveals that the FDA has given the green light to start a Phase II study for their prime candidate, MTX652, targeting Acute Kidney Injury.
On Dec 2, 2023, results from a Penpulimab-based neoadjuvant/adjuvant therapy trial for resectable advanced non-small cell lung cancer were presented at ESMO_ASIA 2023.