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Rechercher sur Study Connect

Active, Not Recruiting

Observational Study of Nivolumab Monotherapy or in Combination With Ipilimumab in Participants With Advanced Melanoma and in Participants With Adjuvant Nivolumab Therapy - CA209-654

Mis à jour: 25 avril, 2022   |   ClinicalTrials.gov

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Impression du resumé

CETTE ÉTUDE CLINIQUE VOUS INTÉRESSE?
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Utiliser le guide de discussion du participant aux essais cliniques pour naviguer dans le processus de participation à une étude clinique. Comprendre les facteurs clés à considérer avant de prendre une décision et poser des questions à votre équipe soignante.

Détails de l’essai

  • Sexe(s)

  • 18+

    Tranche d’âge

  • Active, Not Recruiting

Options de traitement

Groupes de l’étude
INTERVENTION ATTRIBUÉE
Cohort 1: Nivolumab/Ipilimumab combination therapy
Cohort 2: Nivolumab monotherapy
Cohort 3: Nivolumab adjuvant therapy

Principaux critères d’admissibilité

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: For Cohort 1 and 2: (Recruitment ended by 02/20/2020) - Advanced melanoma (Stage III/Stage IV) - Histologically confirmed diagnosis - Treatment decision for nivolumab monotherapy or nivolumab/ipilimumab combination therapy has already been taken For Cohort 3: (Recruitment ended by 08/31/2020) - Primary diagnosis of advanced melanoma after complete surgical tumor resection and no evidence of disease - Treatment decision for adjuvant nivolumab therapy has already been taken Exclusion Criteria: For Cohort 1 and 2: (Recruitment ended by 02/20/2020) - Current primary diagnosis of a cancer other than advanced melanoma, that requires systemic or other treatment or has not been treated curatively (as per discretion of the investigator) - Previous treatment with nivolumab, for nivolumab monotherapy cohort only - Current active participation in an interventional clinical trial For Cohort 3: (Recruitment ended by 08/31/2020) - Current diagnosis of persisting advanced melanoma or a cancer other than advanced melanoma that requires systemic or other treatment or has not been treated curatively (as per discretion of the investigator) - Current active participation in an interventional clinical trial Other protocol-defined inclusion/exclusion criteria apply

Nous vous recommandons fortement de contacter BMS pour signaler les effets secondaires (événements indésirables).
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici.
Signaler des effets secondaires (effets indésirables) ou des plaintes concernant la qualité du produit: Informations médicales

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Des questions? Le support en direct est disponible 24/7 -
Veuillez composer le 833-673-6134 ou Envoyez-nous un courriel