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Clinical Trial Details

Trial ID: L6190
Source ID: NCT02265809
Associated Drug: Aldesleukin
Title: Adaptive Study of IL-2 Dose Frequency on Regulatory T Cells in Type 1 Diabetes
Acronym: DILfrequency
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 1 Diabetes
Interventions: DRUG: Aldesleukin
Outcome Measures: Primary: Change from baseline of CD4 T regulatory cells, CD4 T effector cells and CD25 expression on T regulatory cells during treatment with ultra low dose IL-2, Fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment) | Secondary: T regulatory cell number, phenotype and proliferation, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|T effector cell number, phenotype and proliferation, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Natural Killer cell number, phenotype and proliferation, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|B lymphocyte cell number, phenotype and proliferation, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|T cell and Natural killer cell intracellular signalling, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Full blood count, Measured by automatic analyser, Visits 1-12 (between day -30 and day -1 up to a maximum of approximately day 98 depending on treatment assignment)|Blood levels of IL-2, IL-6, IL-10, TNF-alpha, soluble CD25, IP-10, soluble rIL-6, and CRP, Measured by enzyme-linked immunosorbent assay, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Change in metabolic control, Blood glucose, HbA1c, C-peptide, insulin use and autoantibody status, Visits 1-12 (between day -30 and day -1 up to a maximum of approximately day 98 depending on treatment assignment)|Safety and tolerability, Assessed by clinical history, physical examination, temperature, blood pressure, heart rate, 12-Lead electrocardiogram (ECGs), clinical laboratory tests, and adverse event recording, Visits 1-12 (between day -30 and day -1 up to a maximum of approximately day 98 depending on treatment assignment) | Other: Genotype of T1D associated loci, Measured by immunochip, Visit 1 (between day -30 and day -1)|Gene expression analysis of purified lymphocyte subsets and peripheral blood mononucleated cells, Measured by RNA sequencing, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|IL-2 sensitivity of T regulatory, T effector and NK subsets, Measured by fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Treg suppression and T effector proliferation assays, Measured by radioactive thymidine assay and/or fluorescence-activated cell sorting, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Antigen specific T cell assays, Measured fluorescence-activated cell sorting and/or Enzyme-Linked ImmunoSpot (ELISPOT) assay, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Sysmex® analysis of whole blood, Measured by automatic analyser, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Epigenetic analysis of analysis of purified lymphocyte subsets and peripheral blood, Measured by Bisulphite sequencing of DNA, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Serum/plasma level of cytokines, soluble receptors and inflammatory markers, Measured by enzyme-linked immunosorbent assay, Visits 2-12 (day 0 up to a maximum of approximately day 98 depending on treatment assignment)|Serum/plasma and cellular metabolites, Mass spectrometry, Visits 1-12 (between day -30 and day -1 up to a maximum of approximately day 98 depending on treatment assignment)|Recruitment analysis, Analysis of DILfrequency recruitment database, Visit 1 (between day -30 and day -1)
Sponsor/Collaborators: Sponsor: Cambridge University Hospitals NHS Foundation Trust | Collaborators: University of Cambridge|Sir Jules Thorn Charitable Trust|Juvenile Diabetes Research Foundation|Wellcome Trust|National Institute for Health Research, United Kingdom
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1|PHASE2
Enrollment: 41
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: BASIC_SCIENCE
Start Date: 2014-10-03
Completion Date: 2016-05-26
Results First Posted:
Last Update Posted: 2018-08-21
Locations: Wellcome Trust Clinical Research Facility, Addenbrookes Hospital, Cambridge, Cambridgeshire, CB2 0QQ, United Kingdom
URL: https://clinicaltrials.gov/show/NCT02265809