28
Participants
Start Date
September 21, 2020
Primary Completion Date
September 30, 2023
Study Completion Date
May 20, 2025
Lurbinectedin
"Lurbinectedin will be presented as a lyophilized powder for concentrate for solution for infusion in 4-mg vials. Before use, the 4-mg vial will be reconstituted with 8 mL of sterile water for injection, to give a solution containing 0.5 mg/mL of PM01183. For administration to patients as IV infusion, reconstituted vials will be diluted with glucose 50 mg/mL (5%) or sodium chloride 9 mg/mL (0.9%) solution for infusion.~PM01183 will be administered as a 1 hour IV infusion Q3W, in a minimum volume of 100 mL of solution for infusion (either 5% glucose or 0.9% sodium chloride), or a minimum volume of 250 mL if through a peripheral line, always at a fixed rate and through a pump device."
Pembrolizumab
Pembrolizumab will be supplied as a solution for infusion in a single-use vial. Each vial contains 100 mg of MK3475 (pembrolizumab) in 4 ml of solution. Pembrolizumab 200 mg will be administered as a 30 minute IV infusion Q3W.
Hospital Vall D´Hebrón, Barcelona
ICO - Instituto Catalán de Oncología, Barcelona
Hospital Gregorio Marañon, Madrid
START - Phase I Unit - HN San Chinarro, Madrid
Start - Unidad Fase I - Fundacion Jimenez Diaz, Madrid
Collaborators (1)
MedSIR
OTHER
PharmaMar
INDUSTRY
Merck Sharp & Dohme LLC
INDUSTRY
Antonio Calles Blanco
OTHER