NCT06633354RecruitingEarly phase 1
Targeting CD5 CAR-T Cells in the Treatment of r/r CD5+ T-ALL
A Clinical Study on the Safety and Effectiveness of Targeting CD5 CAR-T Cells in the Treatment of r/r CD5+ T-ALL
Source: ClinicalTrials.gov · Last updated 9 Oct 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
A Clinical Study on the Safety and Effectiveness of targeting CD5 CAR-T Cells in the treatment of r/r CD5+ T-ALL
- Status (registry)
- Recruiting
- Phase (registry)
- Early phase 1
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 8 Oct 2024
- Start date
- 20 Oct 2024
- Primary completion date
- 20 Oct 2027
- Lead sponsor
- Zhejiang University
- NCT number
- NCT06633354
What you commit to
- Study type: Interventional · Early phase 1
- Planned participants: 30
- From 20 Oct 2024 to the primary completion date, 20 Oct 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 5\. Before using any gene therapy products;
- 6\. Received anti-tumor therapy before infusion, should meet the following any one should be ruled out:
- treated with systemic corticosteroids therapy within 72 hours (except glucocorticoid physiological replacement therapy, such as prednisone \< 10 mg/d or an equivalent dose of the drug);
- received within 72 hours of small molecule targeted therapy;
- 2 weeks received systemic chemotherapy except (pretreatment);
- four weeks received radiotherapy;
Other illness
- 1.Patients with the history of epilepsy or other CNS disease;
- 3\. Active infection of hepatitis B virus, C virus or hepatitis E virus;
- 4\. Active infection with no cure;
Lab values
- 2\. Patients with prolonged QT interval time or severe heart disease;
Other
- 7\. The proiferation rate is less than 5 times response to CD3/CD28 co-stimulation signal;
- 8\. Any unsuitable to participate in this trial judged by the investigator;
- 9\. Any situation that researchers believe may increase the risk to the subjects or interfere with the trial results.
Who the study is looking for
- 1\. According to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines for Acute Lymphocytic Leukemia (2020. v1), patients diagnosed as CD5+T-ALL;
- 2\. Consistent with r/r CD5+T-ALL diagnosis, including any of the following conditions:
- No CR after standard chemotherapy;
- The first induction reaches CR, but CR ≤ 12 months;
- Patients with r/r CD5+T-ALL have not responded to the first or multiple remedial treatments;
- c.Multiple recurrences.
- 3\. CD5 expression rate was \>90%;
- 4\. Number of blasts in the bone marrow (protolychic + larvae) \>5% (morphology) and/or \>1% (flow cytometry);
- 5\. Total bilirubin ≤51 (mol/L), Alanine aminotransferase (ALT)/Aspartate aminotransferase (AST) ≤ 3 times the upper limit of the normal range, creatinine ≤176.8 (mol/L);
- 6\. Echocardiography showed left ventricular ejection fraction (LVEF) ≥50%;
- 7.Refers to the pulse oxygen saturation 92% or higher oxygen (state);
- 8.Estimated life expectancy of minimum of 12 weeks;
- 9.ECOG 0-2;
- 10.Pregnant/lactating women, or male or female patients who have fertility and are willing to take effective contraceptive measures at least 6 months after the last cell infusion during the study period;
- 11\. Those who voluntarily participated in this trial and provided informed consent;
Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The first affiliated hospital of medical college of zhejiang university Coordinator of this site? Confirm its status | Hangzhou | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.