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Pfizer C6461006: Phase 1b/2 for metastatic urothelial cancer - Clinical Trial

¿Cuál es el Propósito de este estudio?

To join this study, patients must have a new diagnosis of cervical cancer confirmed by a lab test. The cancer can be one of these types: squamous cell carcinoma, adenocarcinoma, or adenosquamous cell carcinoma. The cancer must be locally advanced, which means it has grown but has not spread far. It can be stage III or stage IVA.

Patients cannot have had their whole uterus removed for cervical cancer, but if part of the uterus was removed for another reason, they can still join. They cannot plan to have their uterus removed as part of their treatment. The cancer cannot have spread to certain lymph nodes high in the body.

Patients must not have had surgery, radiation, or medicine for cervical cancer before. They also cannot have had immunotherapy or radiation to the pelvis for any reason. Patients must be 18 or older.

¿Cuál es la Condición que se está estudiando?

Adults with locally advanced or metastatic urothelial cancer.

¿Quién puede participar en el Estudio?

Adults can join this study if they have urothelial cancer that has spread or is hard to treat with surgery. Before joining, they will have a screening visit where doctors check their health and test if they qualify. People in the study must also agree to give blood, urine, and tissue samples when needed.

Grupo etario
Adultos

¿Qué Implica?

This study is being done to see if PF-08634404 is safe and how it works when given alone or with another medicine called enfortumab vedotin. PF-08634404 is made to help the immune system fight tumors and to reduce the blood that feeds tumor cells. Enfortumab vedotin works by finding and killing cancer cells.

Detalles del Estudio

Título Completo
An Interventional, Phase 1b/2, Open-Label Study to Investigate the Safety, Antitumor Activity, and Pharmacokinetics of PF-08634404 Monotherapy or in Combination With Enfortumab Vedotin in Adult Participants With Locally Advanced or Metastatic Urothelial Cancer, C6461006
Investigador Principal
Número de Protocolo
IRB: PRO00119281
NCT: NCT07421700
Fase
Phase I/II
ClinicalTrials.gov
Estado de inscripción
Pronto disponible para inscripción
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Contribuya a Duke Health