CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 106 enrolled
Drug / intervention
Durvalumab +4 moredrug
Likely dose
Durvalumab 250 mLfrom 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.

Search/NCT02733042
NCT02733042Phase 2Completed

A Phase 1/2, Open-label, Multi-center Study to Assess the Safety and Tolerability of Durvalumab (Anti-PDL1 Antibody) as Monotherapy and in Combination Therapy in Subjects With Lymphoma or Chronic Lymphocitic Leukemia

Celgene·interventional·Posted Apr 11, 2016·Updated Nov 18, 2023

In Brief

A Phase 2 clinical trial evaluating Durvalumab, Lenalidomide, and 3 other interventions for Lymphoma and Leukemia, Lymphocytic, Chronic, B-Cell. Completed, enrolled 106 participants across 66 sites in 7 countries.

Detailed Summary

This study is designed to determine the recommended phase 2 dose (RP2D), and the safety, and efficacy of durvalumab as monotherapy and when given in combination with lenalidomide and rituximab; ibrutinib; or bendamustine and rituximab at the RP2D in adults with lymphoma or chronic lymphocytic leukemia (CLL).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Germany, Italy, Japan, Netherlands, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedApr 11, 2016
Enrollment StartMay 11, 2016
Primary CompletionMar 6, 2019
Study CompletionAug 21, 2022
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 10.2 years ago

Interventions

Durvalumabdrug

Administered as an IV infusion (250 mL) over approximately 1 hour in duration

Lenalidomidedrug

Administered orally

Rituximabdrug

Administered by intravenous infusion

Ibrutinibdrug

Administered orally

Bendamustinedrug

Administered as a 30-minute intravenous infusion