Cáncer Colorectal
Estado: FinalizadoA Phase III, Randomized, Open-label (Sponsor Blinded) Study of Relatlimab-nivolumab Fixed-dose Combination Versus Regorafenib or Trifluridine + Tipiracil (TAS-102) for Participants with Later-lines of Metastatic Colorectal Cancer.
Para inscribirte contáctate a:
[email protected]
Principales Criterios de Inclusión:
Histological confirmed previously treated colorectal cancer with adenocarcinoma histology with metastatic or recurrent unresectable disease at study entry
Participants must have:
- Progressed during or within approximately 3 months following the last administration of approved standard therapies (at least 1, but not more than 4 prior lines of therapies), which must include a fluoropyrimidine, oxaliplatin, irinotecan, an anti-VEGF therapy, and anti-EGFR therapy (if KRAS wild-type), if available in the respective country, or;
- Been intolerant to prior systemic chemotherapy regimens if there is documented evidence of clinically significant intolerance despite adequate supportive measures
- Must have sufficient tumor tissue & evaluable PD-L1 expression to meet the study requirements
- Must have measurable disease per RECIST v1.1. Participants with lesions in a previously irradiated field as the sole site of measurable disease will be permitted to enroll provided the lesion(s) have demonstrated clear progression and can be measured accurately
- Laboratorio:Bristol Myers Squibb
- Área Terapéutica:Oncología
- Fase del estudio:III
- Código de Estudio:CA224-123
- Ver ensayo en Clinical Trials
Santiago
- Centro de Oncología de Precisión
Santiago
- Hospital U. de Chile
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