Actively Recruiting

Age: 18Years +
All Genders
NCT06781450

Study in Patients With Relapsed/Refractory Primary Mediastinal Lymphoma Treated With Pembrolizumab or Nivolumab in Combination With Brentuximab Vedotin in a Real-life Context

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-30

50

Participants Needed

3

Research Sites

188 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Observational, Non-Interventional, Retrospective, Multicenter Study Focusing on the Efficacy and Safety of Pembrolizumab Monotherapy and Nivolumab in Combination With Brentuximab Vedotin in Clinical Practice Patients With Primary Mediastinal B Cell Lymphoma Relapsed/Refractory

CONDITIONS

Official Title

Study in Patients With Relapsed/Refractory Primary Mediastinal Lymphoma Treated With Pembrolizumab or Nivolumab in Combination With Brentuximab Vedotin in a Real-life Context

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed diagnosis of relapsed or refractory Primary Mediastinal B Cell Lymphoma treated with pembrolizumab alone or nivolumab with brentuximab vedotin in real-life practice up to November 2021
  • Age 18 years or older at enrollment
  • Signed written informed consent where applicable
Not Eligible

You will not qualify if you...

  • Patients treated with pembrolizumab alone or nivolumab with brentuximab vedotin within a clinical trial context

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Bologna, Italy, 40138

Actively Recruiting

2

Azienda Ospedaliera Universitaria- POLICLINICO BARI

Bari, Italy, 70124

Actively Recruiting

3

Fondazione IRCCS Istituto Nazionale dei Tumori

Milan, Italy, 20133

Actively Recruiting

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Research Team

P

Pier Luigi Zinzani, MD

CONTACT

C

Cinzia Pellegrini, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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