Recruiting at 16 sites Phase 1 Relapsed/Refractory Multiple Myeloma

Relapsed/Refractory Multiple Myeloma study: CB-011

Official title CRISPR-Edited Allogeneic Anti-BCMA CAR-T Cell Therapy in Patients With Relapsed/Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT05722418

What this study is testing

What is CB-011?

CB-011 is an investigational medicine, being studied as a potential treatment for relapsed/refractory multiple myeloma.

Also referred to as Cyclophosphamide, Fludarabine.

Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This study is testing whether CB-011, a lab-made immune cell therapy, is safe and works in people whose multiple myeloma has come back or does not respond to other treatments.
Who it's for
You may be able to join if you have multiple myeloma that has returned or does not respond to standard treatments.
What's involved
You would receive an infusion of CB-011, a lab-made immune cell. You will have clinic visits for safety checks and tests.
Time commitment
The study lasts several months with visits at the start, then regular check‑ins over the follow‑up period.
  • Phase 1: an early, usually small safety study

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Documented diagnosis of relapsed/refractory multiple myeloma (MM) with measurable disease (according to IMWG diagnostic criteria.)
  • Received at least 3 prior MM treatment lines of therapy which must include a proteasome inhibitor (PI), an immunomodulatory drug (IMiD), and an...
  • Eastern Cooperative Oncology Group performance status grade of 0 or 1.
  • Adequate hematologic, renal, hepatic, pulmonary, and cardiac function.

You likely can't join if

  • Prior treatment with CAR-T cell therapy directed at any target.
  • Autologous stem cell transplant within the last 6 weeks before lymphodepletion.
  • Allogeneic stem cell transplant within 6 months before lymphodepletion.
  • Known active or prior history of CNS involvement.
  • Stroke or seizure within 6 months of signing ICF.
  • Seropositive for or history of human immunodeficiency virus.
See the full eligibility criteria
Who can join
  • Documented diagnosis of relapsed/refractory multiple myeloma (MM) with measurable disease (according to IMWG diagnostic criteria.)
  • Received at least 3 prior MM treatment lines of therapy which must include a proteasome inhibitor (PI), an immunomodulatory drug (IMiD), and an anti-CD38 monoclonal antibody as part of a prior line of therapy, either in...
  • Eastern Cooperative Oncology Group performance status grade of 0 or 1.
  • Adequate hematologic, renal, hepatic, pulmonary, and cardiac function.
What rules you out
  • Prior treatment with CAR-T cell therapy directed at any target.
  • Autologous stem cell transplant within the last 6 weeks before lymphodepletion.
  • Allogeneic stem cell transplant within 6 months before lymphodepletion.
  • Known active or prior history of CNS involvement.
  • Stroke or seizure within 6 months of signing ICF.
  • Seropositive for or history of human immunodeficiency virus.
  • Vaccinated with live, attenuated vaccine within 4 weeks prior to lymphodepletion.
  • Hepatitis B infection.
  • Hepatitis C infection.
  • Known life-threatening allergies, hypersensitivity, or intolerance to CB-011 or its excipients.

The study team makes the final eligibility decision.

Where it is enrolling

  • Birmingham, Alabama, United States
  • Aurora, Colorado, United States
  • Miami, Florida, United States
  • Lexington, Kentucky, United States
  • Hackensack, New Jersey, United States
  • New York, New York, United States
  • Charlotte, North Carolina, United States
  • Durham, North Carolina, United States
  • Cincinnati, Ohio, United States
  • Cleveland, Ohio, United States
  • Nashville, Tennessee, United States
  • Dallas, Texas, United States
  • Salt Lake City, Utah, United States
  • Richmond, Virginia, United States
  • Milwaukee, Wisconsin, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Birmingham, Alabama, United States; Aurora, Colorado, United States; Miami, Florida, United States; Lexington, Kentucky, United States; Hackensack, New Jersey, United States; New York, New York, United States and 9 more locations. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.