50
Participants
Start Date
February 7, 2023
Primary Completion Date
December 14, 2025
Study Completion Date
December 14, 2025
Sacituzumab govitecan
"Upon meeting all selection criteria, patients enrolled in the single-arm study will receive the combination of: sacituzumab govitecan and prophylaxis (loperamide and G-CSF).~Sacituzumab govitecan :10 mg/kg, intravenously (IV) on Days 1 and 8 every 21-day cycle . This treatment will continue until disease progression, unacceptable toxicity, or physician's/patient's decision."
Loperamide
Loperamide : 2 mg orally (PO), twice a day (BID), or 4 mg once a day (QD) during three consecutive days after administration of sacituzumab govitecan, (D2, D3, D4 and D9, D10, D11) during the first two cycles (consider extending to the next cycle at the discretion of the physician).
Granulocyte Colony-Stimulating Factor
G-CSF : 30 MU subcutaneously (SC) QD during two consecutive days, 48 hours after administration of sacituzumab govitecan (D3, D4 and D10, D11) during the first two cycles (consider extending to the next cycle at the discretion of the physician).
Hospital Universitario Donostia, San Sebastián
Hospital Quiron San Camilo- Ruber Juan Bravo, Madrid
Hospital Universitario General de Catalunya, Sant Cugat del Vallès
Hospital Universitario A Coruña, A Coruña
Hospital de Sant Joan Despí - Moises Broggi, Barcelona
Hospital Universitario Clínico San Cecilio de Granada, Granada
Hospital Arnau de Vilanova, Lleida
Hospital Ramón y Cajal, Madrid
Hospital Universitario Virgen del Rocio, Seville
Hospital Quirón Valencia, Valencia
Collaborators (1)
Gilead Sciences
INDUSTRY
MedSIR
OTHER