Early Clinical Study of UTAA09 Injection in the Treatment of Relapsed/Refractory

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Main purpose: To evaluate the safety of UTAA09 injection in the treatment of relapsed/refractory (R/R) autoimmune disease (AID). Secondary purpose: To evaluate the pharmacokinetic (PK) profile of UTAA09 injection in patients with R/R AID. To evaluate the pharmacodynamic (PD) characteristics of UTAA09 injection in patients with R/R AID. To evaluate the initial efficacy of UTAA09 injection in the treatment of R/R AID subjects. To evaluate the immunogenicity of UTAA09 injection in R/R AID subjects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

∙ (3) Histological evidence of non-suppurative destructive cholangitis and small bile duct destruction.

∙ (4) Liver and kidney function, cardiopulmonary function meet the following requirements:

• Creatinine ≤1.5×ULN; (2) Electrocardiogram showed no clinically significant abnormal bands;

⁃ Blood oxygen saturation \>91% in non-oxygen state;

‣ Total bilirubin ≤2×ULN; ALT and AST≤2.5 x ULN; ALT and AST abnormalities due to disease, such as liver infiltration or bile duct obstruction, were determined to be less than 5×ULN. If Gilbert syndrome is diagnosed, the total bilirubin index can be relaxed to ≤3.0×ULN and the direct bilirubin ≤1.5×ULN.

‣ (5) no serious mental disorders; (6) Can understand this test and have signed the informed consent.

Locations
Other Locations
China
PersonGen.Anke Cellular Therapeutice Co., Ltd
RECRUITING
Hefei
Contact Information
Primary
songlou yin, master
yinsonglou@163.com
0516-85806210
Backup
dongmei zhou, doctor
18052268809
Time Frame
Start Date: 2024-04-02
Estimated Completion Date: 2025-03-01
Participants
Target number of participants: 10
Treatments
Experimental: T cell injection targeting CD19 chimeric antigen receptor
Intravenous administration, 1 bag each time (depending on individual differences), dose: 1×108-1×109 CD19-CAR-gdT (UTAA09 injection), the investigator can decide whether to reduce or increase the dose and whether multiple infusions are required according to the condition of the subject
Sponsors
Leads: PersonGen BioTherapeutics (Suzhou) Co., Ltd.

This content was sourced from clinicaltrials.gov

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