3 results
Approved WMOWill not start
Primary: Dose escalation part: To determine the MTD and/or RP2D of PDR001 in combination with regorafenib in patients with metastatic MSS CRC. Expansion part: To evaluate the efficacy based on overall response rate (ORR) of PDR001 in combination…
Approved WMOCompleted
The primary objective of the study is to demonstrate non-inferiority of the KineSpring System, when compared to standard HTO surgery in improving pain and function outcomes at 24 months in patients with primarily unicompartmental medial knee…
Approved WMOPending
This study aims to assess the effectiveness of VRH in reducing itch along with its psychological burden in individuals with chronic itch.