Could licorice root make CAR-T cancer therapy safer and stronger?
NCT ID NCT07616271
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a compound from licorice root, called diammonium glycyrrhizinate, can reduce the toxic side effects and improve the cancer-killing power of CAR-T cell therapy in people with large B-cell lymphoma. About 21 participants will receive either standard care or the licorice extract alongside their CAR-T treatment, and researchers will track side effects and remission rates. The goal is to make this advanced therapy both safer and more effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- diammonium glycyrrhizinate (a compound from licorice root)
- What this could lead to
- If it works, this could make CAR-T cell therapy safer and more effective for people with large B-cell lymphoma.
- What could go wrong
- This is a small, early-stage trial with only 21 participants, so results may not apply to everyone. The treatment requires taking the drug for 2 years, and side effects are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 21 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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May 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years. 2. Patients diagnosed with large B-cell lymphoma and receiving CAR-T cell therapy. 3. Adequate organ function prior to enrollment: ALT and AST ≤ 2.5 × ULN (upper limit of normal); may be extended to ≤5 × ULN in patients with liver involvement; serum total bilirubin \< 34 μmol/L; creatinine clearance \> 30 mL/min; cardiac ejection fraction (EF) ≥ 40%, with no pericardial effusion or significant arrhythmia; room air SpO₂ ≥ 92%. 4. No central nervous system involvement of lymphoma confirmed by MRI prior to enrollment. 5. Subjects of childbearing potential must agree to use highly effective contraceptive methods. 6. The subject or their legal guardian must be able to understand and voluntarily sign a written informed consent form. Exclusion Criteria: 1. Presence of a prior malignancy (other than the disease under study) that requires ongoing systemic treatment for any other malignant tumor. 2. Presence of any life-threatening disease, medical condition, or organ system dysfunction that, in the investigator's judgment, may compromise patient safety or interfere with the interpretation of safety or efficacy data. 3. Current or prior central nervous system (CNS) involvement by malignancy. 4. Receipt of allogeneic stem cell transplantation within 6 months prior to enrollment, or autologous stem cell transplantation within 3 months prior to enrollment; and the patient must have no signs or symptoms of graft-versus-host disease and must not be receiving immunosuppressive therapy. 5. Intolerance or allergy to glycyrrhizic acid preparations. 6. Patient refuses to comply with the study requirements to complete the research work. 7. In the investigator's judgment, the patient is unable to complete the study or comply with the study requirements (due to administrative reasons or other reasons), or is considered unsuitable for clinical trial participation for other reasons.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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