At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 110 enrolled
Drug / intervention
Nivolumab +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Nivolumab and AVD in Early-stage Unfavorable Classical Hodgkin Lymphoma
In Brief
A Phase 2 clinical trial evaluating Nivolumab, Adriamycin, and 2 other interventions for Classical Hodgkin Lymphoma. Completed, enrolled 110 participants across 1 site.
Detailed Summary
The aim of the trial is to improve first-line treatment for early unfavorable cHL by introduction of the anti-PD-1 antibody Nivolumab with a truncated standard chemotherapy (AVD). The primary objective is to show efficacy of the two experimental treatment strategies. Secondary objectives are to further evaluate efficacy, show safety and feasibility and perform correlative studies.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsClassical Hodgkin Lymphoma
CountriesGermany
Collaborators--
Timeline
Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedDec 2016
Enrollment StartFeb 2017
Primary CompletionAug 2022
TodayJul 2026
First PostedDec 29, 2016
Enrollment StartFeb 21, 2017
Primary CompletionAug 22, 2022
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 9.5 years ago
Interventions
Nivolumabdrug
Infusion of Nivolumab
Adriamycindrug
Infusion of Adriamycin
Vinblastinedrug
Infusion of Vinblastine
Dacarbazinedrug
Infusion of Dacarbazine