CI

At a glance

ClinicalIndex Comparison Record
Phase 1Recruiting· 64 target
Drug / intervention
Dose Escalation Phase:CD19.CAR/28 and CD19.CAR/28137 T cells +1 moregenetic
Likely dose
Not stated in record
Key inclusion· 9
  • Diagnosis of recurrent B-cell lymphoma or leukemia (ALL or CLL), or newly diagnosed patients unable to receive or complete standard therapy, or relapsed/refractory aggressive B-cell lymphoma with treatment plan including high dose therapy and autologous stem cell transplantation
  • CD19-positive tumor
  • Age ≤75 years; first 3 patients treated should be ≥18 years
  • Karnofsky or Lansky performance score >60%
Key exclusion· 7
  • Active infection requiring antibiotics (procurement stage)
  • History of other cancer unless successfully treated with curative intent ≥2 years before trial entry (exception: non-melanoma skin cancer, in situ breast or cervix cancer)
  • Currently receiving investigational agents or received tumor vaccines within 6 weeks (PD1/PDL1 inhibitors allowed)
  • History of hypersensitivity reactions to murine protein-containing products

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01853631
NCT01853631Phase 1RecruitingOn TrackUpdated 5mo ago
Long Recruiting

Phase I Study of Activated T-Cells Expressing Second or Third Generation CD19-Specific Chimeric Antigen Receptors for Advanced B-Cell Non-Hodgkin's Lymphoma, Acute Lymphocytic Leukemia and Chronic Lymphocytic Leukemia (SAGAN)

Baylor College of Medicine·interventional·Posted May 15, 2013·Updated Jan 5, 2026

In Brief

A Phase 1 clinical trial evaluating Dose Escalation Phase:CD19.CAR/28 and CD19.CAR/28137 T cells and Expansion Phase: CD19.CAR/28 and CD19.CAR/28137 T cells for Non-Hodgkin Lymphoma and 2 related conditions. Currently recruiting, targeting 64 participants across 2 sites.

Detailed Summary

Subjects on this study have a type of lymph gland cancer called Non-Hodgkin Lymphoma, acute lymphocytic leukemia, or chronic Lymphocytic Leukemia (these diseases will be referred to as "lymphoma" or "leukemia"). The lymphoma or leukemia has come back or has not gone away after treatment. The body has different ways of fighting infection and disease. No one way seems perfect for fighting cancers. This research study combines two different ways of fighting disease, antibodies and T cells, hoping that they will work together. Both antibodies and T cells have been used to treat patients with cancer. They have shown promise, but have not been strong enough to cure most patients. T cells can kill tumor cells but normally there are not enough of them to kill all the tumor cells. Some researchers have taken T cells from a person's blood, grown more of them in the laboratory and then given them back to the person. The antibody used in this study is called anti-CD19. It first came from mice that have developed immunity to human lymphoma. This antibody sticks to lymphoma cells because of a substance on the outside of these cells called CD19. CD19 antibodies have been used to treat people with lymphoma and leukemia. For this study, anti-CD19 has been changed so that instead of floating free in the blood it is now joined to the T cells. When an antibody is joined to a T cell in this way it is called a chimeric receptor. In the laboratory, the investigators found that T cells work better if they also add proteins that stimulate T cells, such as one called CD28. Adding the CD28 makes the cells last longer in the body but not long enough for them to be able to kill the lymphoma cells. The investigators believe that if they add an extra stimulating protein, called CD137, the cells will have a better chance of killing the lymphoma cells. The investigators are going to see if this is true by putting the CD19 chimeric receptor with CD28 alone into half of the cells and the CD19 chimeric receptor with CD28 and CD137 into the other half of the cells. These CD19 chimeric receptor T cells with CD28 and with or without CD137 are investigational products not approved by the FDA. The purpose of this study is to find the biggest dose of chimeric T cells that is safe, to see how long the T cell with each sort of chimeric receptor lasts, to learn what the side effects are and to see whether this therapy might help people with lymphoma or leukemia.

Study Details

Timeline

Phase 1Recruiting
201320142015201620172018201920202021202220232024202520262027202820292030203120322033203420352036
First PostedMay 15, 2013
Enrollment StartFeb 1, 2014
Primary CompletionDec 1, 2026
Study CompletionFeb 1, 2036
TodayJul 2, 2026
Enrollment to primary: 12.8 yearsPosted 13.1 years agoPrimary completion in 5 months

Interventions

Dose Escalation Phase:CD19.CAR/28 and CD19.CAR/28137 T cellsgenetic

Three dose levels will be evaluated. Group 1: CD19.CAR/28137ζ at 1×10\^6 cells/m\^2 and CD19.CAR/28ζ at 1×10\^6 cells/m\^2 Group 2: CD19.CAR/28137ζ at 5×10\^6 cells/m\^2 and CD19.CAR/28ζ at 5×10\^6 cells/m\^2 Group 3: CD19.CAR/28137ζ at 2×10\^7 cells/m\^2 and CD19.CAR/28ζ at 2×10\^7 cells/m\^2

Expansion Phase: CD19.CAR/28 and CD19.CAR/28137 T cellsgenetic

The primary goal of the expanded cohort is to further study the safety profiles of CAR-T cells in each of the disease settings, both with or without lymphodepleting chemotherapy given before CAR-T cell infusion.