NCT06633341RecruitingEarly phase 1
Targeting CD5 CAR-T Cells in the Treatment of r/r CD5+ T-lymphoma
A Clinical Study on the Safety and Effectiveness of Targeting CD5 CAR-T Cells in the Treatment of r/r CD5+ T-lymphoma
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-lymphoma
- 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
- Diseases
- Childhood cancers
- NCT number
- NCT06633341
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\. History of epilepsy or other central nervous system disorders;
- 3\. Active infection of hepatitis B virus, C virus or hepatitis E virus;
- 4\. Active infected persons who are not cured;
Lab values
- 2\. Electrocardiogram shows prolonged QT interval, severe heart diseases such as severe arrhythmia in the past;
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 2016 WHO classification of lymphocyte tumors, histologically confirmed CD5-positive T-cell non-Hodgkin lymphoma (T-NHL),
- R/R T-NHL(meets one of the following conditions) :
- Subjects did not go into remission or relapse after receiving second-line or more chemotherapy regiments;
- Primary drug resistance;
- Relapse after autologous hematopoietic stem cell transplantation;
- 2.CD5 expression rate was \>90%;
- 3\. According to Lugano 2014, there should be at least one evaluable tumor lesion;
- 4\. 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);
- 5\. Echocardiography showed left ventricular ejection fraction (LVEF) ≥50%;
- 6\. Refers to the pulse oxygen saturation 92% or higher oxygen (state);
- 7\. Estimated life expectancy of minimum of 12 weeks;
- 8\. ECOG 0-2;
- 9\. 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;
- 10\. 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.