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NCT05366569Recruiting

Bio-CAR-T BS Study

Bio-CAR-T Study on Pre and Post-infusion CAR-T Cell Therapy

Source: ClinicalTrials.gov · Last updated 30 Apr 2026

Brief summary (registry, in English)

The aim of this Study is the evaluation of post-infusion CAR-T (Chimeric Antigen Receptor T Cell) expansion and persistence in patients with DLBCL, PMBCL and ALL undergoing CAR-T therapy; and the feasibility and efficacy of the treatment in the real life practice.

Status (registry)
Recruiting
Study type
Observational
Enrollment
45 (estimated)
First submitted
22 Apr 2022
Start date
26 Apr 2022
Primary completion date
31 Dec 2026
Lead sponsor
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
NCT number
NCT05366569

What you commit to

  • Study type: Observational
  • Planned participants: 45
  • From 26 Apr 2022 to the primary completion date, 31 Dec 2026
  • 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.

Other illness

  • Active or uncontrolled infections;
  • Presence of clinically relevant co-morbidities (e.g., select cardiovascular, neurologic, or immune disorders with organ dysfunction or requiring immunosuppressive treatment in the last 24 months);

Age

  • Patients with B-cell-ALL \> 25 years
  • Patients with DLBCL \<18 or \>70 years
  • Patients with PMBCL \<18 or \>70 years

Other

  • Performance status \> 1;
  • Thrombo-embolisms within the last 6 months;
  • Life expectancy \< 3 months.

Who the study is looking for

  • Patients with B-cell-ALL (≤ 25 years) or patients with DLBCL (18-70 years) or patients with PMBCL (18-70 years) who were relapsed/refractory after two lines of treatments;
  • Adequate performance status (0 or 1);
  • Adequate organ function;
  • No active or uncontrolled infections;
  • No thrombo-embolisms within the last 6 months;
  • Absence of clinically relevant co-morbidities (e.g., select cardiovascular, neurologic, or immune disorders with organ dysfunction or requiring immunosuppressive treatment in the last 24 months);
  • Life expectancy of at least 3 months.

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
ASST Spedali Civili di Brescia
Coordinator of this site? Confirm its status
BresciaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.