CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 86 enrolled
Drug / intervention
PCI 32765drug
Likely dose
PCI 32765 420 mgfrom 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/NCT01500733
NCT01500733Phase 2Active

A Phase II Study of PCI-32765 for Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) Who Need Therapy and Are Older Than 65 or Have a 17p Deletion

National Heart, Lung, and Blood Institute (NHLBI)·interventional·Posted Dec 28, 2011·Updated Apr 28, 2026

In Brief

A Phase 2 clinical trial evaluating PCI 32765 for Leukemia and 3 related conditions. Active but no longer recruiting, targeting 86 participants across 1 site.

Detailed Summary

Background: \- Chronic lymphocytic leukemia and small lymphocytic lymphoma (CLL/SLL) are types of blood or lymph node cancers that mostly affect the elderly. CLL/SLL both create abnormal white blood cells that hurt the immune system and make it more difficult to fight infections. These cancers are usually diagnosed after age 50; more than half of the people with CLL/SLL are over age 70. Elderly people often do not respond well to standard chemotherapy for CLL/SLL. They may have other health problems that make chemotherapy difficult. In addition, individuals who have a genetic abnormality called 17p deletion also do not respond well to standard treatments for CLL/SLL. Researchers want to test a new cancer treatment drug, PCI-32765, to see if it can treat CLL/SLL in these hard-to-treat groups. Objectives: \- To see if PCI-32765 is a safe and effective treatment for CLL/SLL in older people and people with 17p deletion. Eligibility: * Individuals over 65 years of age who have CLL/SLL. * Individuals at least 18 years of age who have CLL/SLL and 17p deletion. Design: * Participants will be screened with a medical history, physical exam, and imaging studies. Blood and urine samples will be taken. Optional bone marrow and lymph node biopsies may also be taken. * Participants will take PCI-32765 capsules every day for 28 days (one cycle of treatment). Treatment will be monitored with frequent blood tests and clinic visits. * PCI-32765 will be given for six cycles of treatment. Those who benefit from the drug will continue to take it as long as there are no side effects and the disease does not progress. Those who do not benefit will stop treatment and have regular followup exams.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Active
201220132014201520162017201820192020202120222023202420252026202720282029203020312032203320342035
First PostedDec 28, 2011
Enrollment StartJan 5, 2012
Primary CompletionJun 20, 2014
Study CompletionSep 30, 2034
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 14.5 years ago

Interventions

PCI 32765drug

420 mg daily