At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 70 enrolled
Drug / intervention
Tislelizumabdrug
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.
A Single Arm, Multicenter, Phase 2 Study of BGB-A317 as Monotherapy in Relapsed or Refractory Classical Hodgkin Lymphoma
In Brief
A Phase 2 clinical trial evaluating Tislelizumab for Classical Hodgkin Lymphoma. Completed, enrolled 70 participants across 12 sites.
Detailed Summary
The primary objective of this study was to evaluate the efficacy of tislelizumab assessed by Independent Review Committee (IRC) in participants with relapsed or refractory classical Hodgkin lymphoma (cHL), as measured by Overall Response Rate (ORR) per the Lugano Classification
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsClassical Hodgkin Lymphoma
CountriesChina
Collaborators--
Timeline
Phase 2CompletedFinished
201820192020202120222023202420252026
Enrollment StartApr 2017
First PostedJul 2017
Primary CompletionNov 2020
TodayJul 2026
First PostedJul 6, 2017
Enrollment StartApr 21, 2017
Primary CompletionNov 2, 2020
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 9.0 years ago
Interventions
Tislelizumabdrug
Administered as specified in the treatment arm