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Ícono de BMS, estudio Activo, no reclutando

Active, Not Recruiting

ID del estudio CA209-8RX  |   NCT03771859

A Study of Patients Receiving Adjuvant Nivolumab Therapy for Melanoma That Has Been Removed

Ícono de advertencia
Lo sentimos, este estudio ya no acepta nuevos participantes, pero aún está en curso.
Puede hacer clic en el botón “Verificar su Elegibilidad” y responder algunas preguntas sobre su salud para averiguar si podría ser compatible con otro estudio.
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Resumen

  • Ícono de género masculino y femenino
  • 18+
  • Ícono de BMS, estudio Activo, no reclutando
    Active, Not Recruiting

Descripción general

A study in melanoma patients with involvement of lymph nodes or disease that has spread who have undergone complete removal and are eligible for adjuvant treatment with nivolumab

Criterios clave de elegibilidad

Inclusion Criteria: - Patients with a primary diagnosis of melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection and have no evidence of disease. - Decision to treat with adjuvant nivolumab therapy has already been taken - At least 18 years of age at the time of treatment decision - Patients who provide written informed consent to participate in the study Exclusion Criteria: - Any patient with a current diagnosis of persisting advanced melanoma - Any patient currently enrolled in an interventional clinical trial for his/her melanoma treatment (note: patients who have completed their participation in an interventional trial or who are no longer receiving the study drug and are only followed up for OS/RFS can be enrolled. In case of a blinded study, the treatment arm needs to be known). Other protocol defined inclusion/exclusion criteria could apply

Opciones de tratamiento

Brazos del estudio

INTERVENCIÓN ASIGNADA

Brazos del estudio

Participants who initiate adjuvant treatment with nivolumab

INTERVENCIÓN ASIGNADA

Recomendamos encarecidamente que se comunique con BMS para informar los efectos secundarios (eventos adversos)
Los efectos secundarios (eventos adversos) y otros eventos reportables se definen aquí
Informe de efectos secundarios (eventos adversos) o quejas sobre la calidad del producto: información médica

¿Tiene alguna pregunta? El soporte en vivo está disponible 24/7 - Llame 855-907-3286 o Envíenos un correo electrónico

¿Tiene alguna pregunta? El soporte en vivo está disponible 24/7 -
Llame 855-907-3286 o Envíenos un correo electrónico