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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04397107
Other study ID # 20K013-001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 15, 2020
Est. completion date June 30, 2022

Study information

Verified date August 2022
Source The First Hospital of Jilin University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to explore the therapeutic value and mechanism of Interleukin-2 on children with rheumatic diseases (Systemic Lupus Erythematosus, Primary Sjögren Syndrome, Juvenile Idiopathic Arthritis).


Description:

The investigators designed a single center, open-label, prospective study that routinely administered low-dose IL-2 therapy to monitor the improvement of clinical and laboratory parameters to explore its efficacy and to observe changes in immune cell subsets and cytokines. Methods: Patients were divided into two groups. One received standard therapy, while another one administrate with low-does IL-2 plus standard therapy.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date June 30, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 17 Years
Eligibility Inclusion Criteria: 1. age <18 years old 2. meet the diagnostic criteria of disease classification 3. HIV negative;Negative for Hepatitis B Virus and Hepatitis C Virus. Exclusion Criteria: 1. heart failure (cardiac function = grade III NYHA) 2. liver insufficiency (upper limit of normal range of transaminase > 2 times) 3. renal insufficiency (creatinine clearance =30ml/min) 4. acute or severe infections such as bacteremia and sepsis 5. malignant tumor 6. high-dose steroid pulse therapy or intravenous injection of glucocorticoids in the last 1 month;Rituximab, infliximab or other biological agents were used 7. mental disorders or any other chronic illness or substance abuse may interfere with the ability to comply with agreements or provide information 8. Inability to comply with IL-2 treatment regimen.

Study Design


Intervention

Drug:
IL-2
Patients were received low dose recombinant human Interleukin-2

Locations

Country Name City State
China Sirui Yang Changchun Changchun/Jilin

Sponsors (1)

Lead Sponsor Collaborator
The First Hospital of Jilin University

Country where clinical trial is conducted

China, 

References & Publications (4)

Cheng G, Yu A, Malek TR. T-cell tolerance and the multi-functional role of IL-2R signaling in T-regulatory cells. Immunol Rev. 2011 May;241(1):63-76. doi: 10.1111/j.1600-065X.2011.01004.x. Review. — View Citation

Fontenot JD, Rasmussen JP, Gavin MA, Rudensky AY. A function for interleukin 2 in Foxp3-expressing regulatory T cells. Nat Immunol. 2005 Nov;6(11):1142-51. Epub 2005 Oct 16. Erratum in: Nat Immunol. 2006 Apr;7(4):427. — View Citation

Malek TR. The biology of interleukin-2. Annu Rev Immunol. 2008;26:453-79. Review. — View Citation

Rosenzwajg M, Lorenzon R, Cacoub P, Pham HP, Pitoiset F, El Soufi K, RIbet C, Bernard C, Aractingi S, Banneville B, Beaugerie L, Berenbaum F, Champey J, Chazouilleres O, Corpechot C, Fautrel B, Mekinian A, Regnier E, Saadoun D, Salem JE, Sellam J, Seksik P, Daguenel-Nguyen A, Doppler V, Mariau J, Vicaut E, Klatzmann D. Immunological and clinical effects of low-dose interleukin-2 across 11 autoimmune diseases in a single, open clinical trial. Ann Rheum Dis. 2019 Feb;78(2):209-217. doi: 10.1136/annrheumdis-2018-214229. Epub 2018 Nov 24. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in steroid dose and immunosuppressor dose at 1 year compared to control group The average daily doses of steroid and immunosuppressor per square meter was recorded 1 year
Secondary The Immunologic Impact of IL-2 Treatment Laboratory measures were detected, including, C3, C4 and anti-dsDNA titres. 1 month,3 month,6 month,1 year
Secondary Immunological Responses Enumeration of the number of subjects with a change in the absolute number of immune cells and serum cytokines in the peripheral blood 1 month,3 month,6 month,1 year
Secondary Change from baseline in SELENA SLEDAI Score Assessment version of the SLE Disease Activity Index (SELENA-SLEDAI) change. The higher the score represent the worse of the disease. The total score ranges from 0 to 105 points. 1 month,3 month,6 month,1 year
Secondary Change from baseline in EULAR SS disease activity index Low-activity (ESSDAI<5),moderate-activity (5=ESSDAI=13) ,high-activity (ESSDAI=14) levels. 1 month,3 month,6 month,1 year
Secondary Incidence of adverse drug reactions Adverse events includes injection site reactions, influenza-like symptoms, infection, fever, tumor, cardiovascular event,drug-induced liver and kidney damage. up to 1 year
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