Your session is about to expire
← Back to Search
Anti-tumor antibiotic
Bendamustine + Venetoclax + Rituximab for Chronic Lymphocytic Leukemia
Phase 2
Waitlist Available
Led By Nicole Lamanna, MD
Research Sponsored by Nicole Lamanna
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Eastern Oncology Cooperative Group (ECOG) performance score of ≤ 2
Age ≥ 18 years of age
Must not have
Treatment with steroid therapy for anti-neoplastic intent, moderate or strong CYP3A inhibitors, or inducers within 7 days prior to the first dose of study drug
Received an allogeneic stem cell transplant
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 15 months
Awards & highlights
No Placebo-Only Group
All Individual Drugs Already Approved
Approved for 5 Other Conditions
Summary
This trial will test if the addition of venetoclax to bendamustine and rituximab can safely and effectively treat patients with relapsed or refractory CLL.
Who is the study for?
Adults diagnosed with Chronic Lymphocytic Leukemia (CLL) who have not had prior treatment for their condition, except corticosteroids for symptom relief. Participants must be over 18, able to use contraception, and have adequate organ function. Excluded are those with allergies to trial drugs, active non-CLL cancers within the last 2 years (with some exceptions), significant health issues as assessed by the investigator, or current severe infections.
What is being tested?
The study is testing a combination of treatments: initially Bendamustine and Rituximab (BR) followed by Venetoclax plus Rituximab for CLL. The total therapy duration is 15 months. Venetoclax targets a protein on CLL cells but requires hospital monitoring due to risk of tumor lysis syndrome—a potentially fatal complication from rapid cancer cell breakdown.
What are the potential side effects?
Potential side effects include reactions related to immune system suppression such as infection risks; infusion-related reactions; blood electrolyte imbalances leading to kidney failure or other serious conditions due to tumor lysis syndrome; and general side effects like fatigue or digestive disturbances.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can take care of myself but might not be able to do heavy physical work.
Select...
I am 18 years old or older.
Select...
I have not received any treatment for CLL, except possibly corticosteroids for other conditions.
Select...
I have been diagnosed with chronic lymphocytic leukemia (CLL).
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I haven't taken steroids or certain strong medications for cancer within the last week.
Select...
I have received a stem cell transplant from a donor.
Select...
I am currently being treated for an autoimmune disease.
Select...
I do not have an active infection, hepatitis B or C, HIV, or serious heart issues.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 15 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~15 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Overall response rate (ORR) after the completion of all therapy
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
Trial Design
1Treatment groups
Experimental Treatment
Group I: BR followed by venetoclax and rituximabExperimental Treatment3 Interventions
Subjects will be on Bendamustine 50-90 mg/m2 on days 1-2 for three cycles with each cycle being 28 days, and Rituximab 375 mg/m2 on day 1 or days 1-2 for three cycles with each cycle being 28 days. Venetoclax will then be started in a step-wise fashion per the package insert.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Venetoclax
FDA approved
Bendamustine
FDA approved
Rituximab
FDA approved
Find a Location
Who is running the clinical trial?
Nicole LamannaLead Sponsor
Nicole Lamanna, MD5.013 ReviewsPrincipal Investigator - Columbia University
Columbia University
2 Previous Clinical Trials
219 Total Patients Enrolled
5Patient Review
I feel incredibly lucky to have been Dr. Lamanna's patient for the last 16 years. Not only is she caring, but she also stays current with all the latest breakthroughs and updates. I have complete confidence in her.
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My liver is working well.I am using or willing to use birth control.I do not have any uncontrolled health conditions.I can take care of myself but might not be able to do heavy physical work.I have been treated for CLL or SLL, but only with corticosteroids for symptoms.I haven't taken steroids or certain strong medications for cancer within the last week.I am 18 years old or older.I have received a stem cell transplant from a donor.I haven't had any cancer other than CLL in the last 2 years.I am currently being treated for an autoimmune disease.I have not received any treatment for CLL, except possibly corticosteroids for other conditions.I do not have an active infection, hepatitis B or C, HIV, or serious heart issues.I have been diagnosed with chronic lymphocytic leukemia (CLL).
Research Study Groups:
This trial has the following groups:- Group 1: BR followed by venetoclax and rituximab
Awards:
This trial has 3 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 5 Other Conditions - This treatment demonstrated efficacy for 5 other conditions.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger