About this trial

To observe the safety and efficacy of Nanobody-Based CD5-targeted chimeric antigen receptor T cells in the treatment of refractory or relapsed T-ALL/NHL

Eligibility criteria

Qualifiers

The subject or guardian understands and voluntarily signs the informed consent form (ICF).

Male or female, aged 3-70 years at the time of signing the ICF (inclusive).

Expected survival of at least 12 weeks.

ECOG performance status of 0-2 at the time of ICF signing.

Disqualifiers

Epilepsy

Paralysis

Aphasia

Stroke

Trial design

Treatments tested in this trial

  • CD5-targeted CAR-T cells

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

1
Peking University People's Hospital100044, BeijingBeijing Municipality, China

Sponsors and collaborators

Peking University People's Hospital

Lead sponsor

Hebei Senlang Biotechnology Inc., Ltd.

Collaborator