3 results
Approved WMORecruitment stopped
Primary: to characterize the safety and tolerability of GSK3052230 in combination with chemotherapy regimens, to determine the MTD and to assess overall response rate in patients with stage IV or recurrent squamous NSCLC with FGFR1 gene…
Approved WMOPending
The aim of this study is to evaluate the efficacy of a personalized drug profiling method using short-term cultures of malignant cells derived from the patient*s pleural fluid.
Approved WMORecruiting
This study has been transitioned to CTIS with ID 2024-513217-12-00 check the CTIS register for the current data. To determine the activity and safety of nivolumab (as monotherapy or in combination with other immunomodulatory treatments) after…