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Completed Phase 1Phase 2 Interventional Results available

Akt Inhibitor MK2206, Bendamustine Hydrochloride, and Rituximab in Treating Patients With Relapsed Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

ClinicalTrials.gov ID: NCT01369849

Public ClinicalTrials.gov record NCT01369849. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 2:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase I/II Study of the Combination of Bendamustine, Rituximab and MK-2206 in the Treatment of Relapsed Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I/II trial studies the side effects and best dose of v-akt murine thymoma viral oncogene homolog 1 (Akt) inhibitor MK2206 when given together with bendamustine hydrochloride and rituximab and to see how well they work in treating patients with refractory chronic lymphocytic leukemia or small lymphocytic lymphoma. Akt inhibitor MK2206 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as bendamustine hydrochloride, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving Akt inhibitor MK2206 with bendamustine hydrochloride and rituximab may be an effective treatment for relapsed chronic lymphocytic leukemia or small lymphocytic lymphoma.

Study identification

NCT ID
NCT01369849
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
15 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2011
Primary completion
Jan 31, 2014
Completion
Jan 31, 2014
Last update posted
Sep 14, 2017

2011 – 2014

United States locations

U.S. sites
44
U.S. states
5
U.S. cities
32
Facility City State ZIP Site status
Mayo Clinic in Arizona Scottsdale Arizona 85259
Siouxland Regional Cancer Center Sioux City Iowa 51101
Mercy Medical Center-Sioux City Sioux City Iowa 51104
Saint Luke's Regional Medical Center Sioux City Iowa 51104
Essentia Health Saint Joseph's Medical Center Brainerd Minnesota 56401
Fairview Ridges Hospital Burnsville Minnesota 55337
Mercy Hospital Coon Rapids Minnesota 55433
Essentia Health Cancer Center Duluth Minnesota 55805
Essentia Health Saint Mary's Medical Center Duluth Minnesota 55805
Miller-Dwan Hospital Duluth Minnesota 55805
Fairview-Southdale Hospital Edina Minnesota 55435
Unity Hospital Fridley Minnesota 55432
Hutchinson Area Health Care Hutchinson Minnesota 55350
Minnesota Oncology Hematology PA-Maplewood Maplewood Minnesota 55109
Saint John's Hospital - Healtheast Maplewood Minnesota 55109
Abbott-Northwestern Hospital Minneapolis Minnesota 55407
Hennepin County Medical Center Minneapolis Minnesota 55415
North Memorial Medical Health Center Robbinsdale Minnesota 55422
Mayo Clinic Rochester Minnesota 55905
Metro-Minnesota NCI Community Oncology Research Program Saint Louis Park Minnesota 55416
Park Nicollet Clinic - Saint Louis Park Saint Louis Park Minnesota 55416
Regions Hospital Saint Paul Minnesota 55101
United Hospital Saint Paul Minnesota 55102
Saint Francis Regional Medical Center Shakopee Minnesota 55379
Lakeview Hospital Stillwater Minnesota 55082
Ridgeview Medical Center Waconia Minnesota 55387
Rice Memorial Hospital Willmar Minnesota 56201
Minnesota Oncology and Hematology PA-Woodbury Woodbury Minnesota 55125
Adena Regional Medical Center Chillicothe Ohio 45601
Riverside Methodist Hospital Columbus Ohio 43214
Columbus CCOP Columbus Ohio 43215
Grant Medical Center Columbus Ohio 43215
Mount Carmel Health Center West Columbus Ohio 43222
Doctors Hospital Columbus Ohio 43228
Grady Memorial Hospital Delaware Ohio 43015
Fairfield Medical Center Lancaster Ohio 43130
Marietta Memorial Hospital Marietta Ohio 45750
Knox Community Hospital Mount Vernon Ohio 43050
Licking Memorial Hospital Newark Ohio 43055
Southern Ohio Medical Center Portsmouth Ohio 45662
Springfield Regional Medical Center Springfield Ohio 45505
Saint Ann's Hospital Westerville Ohio 43081
Genesis HealthCare System Zanesville Ohio 43701
Rapid City Regional Hospital Rapid City South Dakota 57701

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01369849, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 14, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01369849 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →