IgG4-Related Disease Clinical Trials

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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
Related Therapeutic Areas
Myositis
IgG4-Related Disease
Systemic Lupus Erythematosus (SLE)
Scleroderma
Systemic Sclerosis (SSc)
Sponsors
Leads: PersonGen BioTherapeutics (Suzhou) Co., Ltd.

This content was sourced from clinicaltrials.gov

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