Preventive stRategy for IMMU132-relatED AEs in TNBC - PRIMED

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

February 7, 2023

Primary Completion Date

December 14, 2025

Study Completion Date

December 14, 2025

Conditions
Triple Negative Breast CancerBreast Cancer
Interventions
DRUG

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."

DRUG

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).

DRUG

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).

Trial Locations (10)

20014

Hospital Universitario Donostia, San Sebastián

28006

Hospital Quiron San Camilo- Ruber Juan Bravo, Madrid

08190

Hospital Universitario General de Catalunya, Sant Cugat del Vallès

Unknown

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

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Gilead Sciences

INDUSTRY

lead

MedSIR

OTHER