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Phase I study to evaluate the safety and tolerability of GS-4528 in monotherapy and in combination with an anti-PD-1 monoclonal antibody in adults with advanced solid tumors.

EL OBJETIVO ES ANALIZAR UN NUEVO FÁRMACO EN INVESTIGACIÓN LLAMADO GS-4528 EN MONOTERAPIA Y EN COMBINACIÓN CON ZIMBERELIMAB (ZIM) EN SERES HUMANOS PARA COMPROBAR SI ES SEGURO Y TOLERABLE EN EL TRATAMIENTO DE PACIENTES CON DIFERENTES TIPOS DE CÁNCER

Status
In recruitment
headquarters
Pamplona/Madrid
Early phase

Technical Summary

  • ESTUDIO DE FASE I PARA EVALUAR LA SEGURIDAD Y TOLERABILIDAD DE GS-4528 EN MONOTERAPIA Y EN COMBINACIÓN CON UN ANTICUERPO MONOCLONAL ANTIPD-1 EN ADULTOS CON TUMORES SÓLIDOS AVANZADOS
  • Code EudraCT: .
  • Protocol number: GS-US-616-6291
  • Promoter: Gilead Science

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

More information about this clinical trial

Information offered by the Spanish Registry of Clinical Studies

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