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Characterization of Natural IL-6 Inhibition in Healthy Individuals (FIDI)

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University of Copenhagen

Status

Enrolling

Conditions

Autoantibodies
Interleukin-6

Treatments

Other: Cycling test
Other: Oral Glucose Tolerance Test

Study type

Interventional

Funder types

Other

Identifiers

NCT05867524
H-20082776

Details and patient eligibility

About

The aim of the project is to investigate whether or not there are any difference in cardiometabolic outcomes in individuals with high or low levels of c-aAb against interleukin-6 (IL-6).

The study is the first to investigate individuals with extreme amounts of c-aAb levels against IL-6 and to contribute with knowledge on a possible new phenotype.

Enrollment

40 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Fulfill Danish blood donor criteria
  • Have extreme amounts of IL-6 c-aAb or matched as control (low amounts of IL-6 c-aAb)

Exclusion criteria

  • Failure to fulfill Danish blood donor criteria

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

High IL-6 c-aAb
Experimental group
Description:
Individuals with top percentile IL-6 c-aAb
Treatment:
Other: Cycling test
Other: Oral Glucose Tolerance Test
Low IL-6 c-aAb
Experimental group
Description:
Individually matched controls with low IL-6 c-aAb
Treatment:
Other: Cycling test
Other: Oral Glucose Tolerance Test

Trial contacts and locations

1

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Central trial contact

Rasmus T Jensen, MSc; Torben Hansen, PhD

Data sourced from clinicaltrials.gov

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