CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 48 enrolled
Drug / intervention
Carfilzomib +7 moredrug
Likely dose
Carfilzomib 11 mg/m2from 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/NCT02073097
NCT02073097Phase 2Completed

A Phase I/II Study of Carfilzomib in Combination With R-CHOP (CR-CHOP) for Patients With Diffuse Large B-cell Lymphoma

Case Comprehensive Cancer Center·interventional·Posted Feb 27, 2014·Updated May 29, 2024

In Brief

A Phase 2 clinical trial evaluating Carfilzomib, Rituximab, and 6 other interventions for Contiguous Stage II Adult Diffuse Large Cell Lymphoma and 4 related conditions. Completed, enrolled 48 participants across 3 sites.

Detailed Summary

This phase I/II trial studies the side effects and best dose of carfilzomib when given together with rituximab and combination chemotherapy and to see how well they work in treating patients with diffuse large B-cell lymphoma. Carfilzomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as rituximab, can block cancer growth by finding cancer cells and helping kill them. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. It is not known if carfilzomib in combination with R-CHOP is better or worse than R-CHOP alone in treating patients with diffuse large b-cell lymphoma.

Study Details

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedFeb 27, 2014
Enrollment StartJan 28, 2015
Primary CompletionJul 20, 2021
Study CompletionJun 29, 2023
TodayJul 2, 2026
Enrollment to primary: 6.5 yearsPosted 12.3 years ago

Interventions

Carfilzomibdrug

Given IV, according to dose level. Cohorts begin with dose level (DL)1, escalated in standard 3+3 design to identify a recommended phase 2 dose DL (-2) 11 mg/m2 on day 1 and 2 every 21 days, cycles 1-6 DL (-1) 15 mg/m2 on days 1 and 2 every 21 days, cycles 1-6 DL (1) 20 mg/m2 days 1,2 every 21 days, cycles 1-6 DL (2) 20 mg/m2 days 1,2 of cycle 1 followed by 27 mg/m2 days 1,2 every 21 days for cycles 2-6. DL (3) 20 mg/m2 days 1,2 of cycle 1 followed by 36 mg/m2 days 1,2 every 21 days for cycles 2-6. DL(4) 20 mg/m2 days 1,2 of cycle 1 followed by 45 mg/m2 days 1,2 every 21 days for cycles 2-6 DL (5) 20 mg/m2 days 1,2 of cycle 1 followed by 56 mg/m2 days 1,2 every 21 days for cycles 2-6

Rituximabbiological

Given IV (375mg/m\^2)

Cyclophosphamidedrug

Given IV (750mg/m\^2)

Doxorubicin hydrochloridedrug

Given IV (50mg/m\^2)

Vincristine sulfatedrug

Given IV (1.4mg/m\^2)

Prednisonedrug

Given PO (100mg)

Pegfilgrastimdrug

6 mg SC day 4 (every 21 days). Filgrastim 300 or 480 mcg IV/SC daily days 1-10 may be substituted if pegfilgrastim is not available. ONPROTM is also an acceptable method of administration.

Acyclovirdrug

PO (400mg)