Study of Nivolumab in Patients With Classical Hodgkin's Lymphoma (Registrational)
Completed · Phase 2
Conditions studied: Hodgkin Disease
In brief
The purpose of this study is to evaluate the efficacy and safety of Nivolumab in previously treated (cohorts, A, B \& C) or newly diagnosed (cohort D) classical Hodgkin Lymphoma participants.
Key facts
- Study ID
- NCT02181738
- Run by
- Bristol-Myers Squibb
- People needed
- 294
- Starts
- 2014-08-12
- Expected to finish
- 2022-12-27
- Last updated by the study team
- 2023-11-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
- Must have received prior high-dose conditioning chemotherapy followed by autologous stem cell transplant (ASCT) as a part of salvage therapy for cHL (cohort A, B \& C - enrollment closed)
- Participants may be Brentuximab vedotin- naïve, or may have had prior Brentuximab vedotin treatment (cohort A, B \& C - enrollment closed)
- Newly diagnosed and previously untreated classical Hodgkin Lymphoma (cohort D)
You may not qualify if…
- Known central nervous system lymphoma
- Participants with nodular lymphocyte-predominant Hodgkin Lymphoma
- Prior allogeneic stem cell transplantation (SCT)
- Chest radiation ≤ 24 weeks prior to first dose
- Carmustine ≥ 600 mg/m² received as part of the pre-transplant conditioning regimen
Where it is running
- Local Institution - 0030 — Los Angeles, California, United States
- Local Institution - 0009 — Los Angeles, California, United States
- Local Institution - 0001 — Atlanta, Georgia, United States
- Local Institution - 0002 — Boston, Massachusetts, United States
- Local Institution - 0025 — Boston, Massachusetts, United States
- Local Institution - 0041 — Boston, Massachusetts, United States
- Local Institution - 0008 — Detroit, Michigan, United States
- Local Institution - 0003 — Rochester, Minnesota, United States
- Local Institution - 0047 — Hackensack, New Jersey, United States
- Local Institution - 0040 — Basking Ridge, New York, United States
- Local Institution - 0005 — New York, New York, United States
- Local Institution - 0006 — Allentown, Pennsylvania, United States
- Local Institution - 0004 — Nashville, Tennessee, United States
- Local Institution - 0007 — Houston, Texas, United States
- Local Institution - 0032 — Innsbruck, Austria
- Local Institution - 0031 — Vienna, Austria
- Local Institution - 0014 — B-leuven, Belgium
- Local Institution - 0015 — Ghent, Belgium
- Local Institution - 0046 — Vancouver, British Columbia, Canada
- Local Institution - 0042 — Toronto, Ontario, Canada
- Local Institution - 0044 — Prague, Czechia
- Local Institution - 0037 — Berlin, Germany
- Local Institution - 0033 — Cologne, Germany
- Local Institution - 0036 — Hamburg, Germany
- Local Institution - 0034 — Ulm, Germany
Full record on ClinicalTrials.gov
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