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Completed

NCT Number: NCT02955615

ILT-101 in Patients With Active Moderate to Severe Systemic Lupus Erythematosus (SLE)

The purpose of this study is to evaluate the efficacy and safety of ILT-101 (human recombinant interleukin 2 (IL-2)) in patients with moderate to severe systemic lupus erythematosus.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

AKH Wien, Vienna, Austria

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About this study

Interleukin 2 (IL-2) plays an important role on immune homeostasis by acting on T lymphocytes. In systemic lupus erythematosus, there is a so called "insufficiency" in a subpopulation of T lymphocytes, the regulatory T cells (Tregs) leading to altered immune balance between regulatory and effector T cells. These cells seem to play a major role in the physiopathology of the disease. Many researches enlighten the fact that this Tregs/Teffs balance can be restored by administering low dose of IL-2. It is thus assumed that treatment with low dose of IL-2 may impact positively the progression of the disease and thus help patients improving their clinical outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed diagnosis of SLE
  • Active SLE
  • On stable background therapy for 1 month
  • Using highly effective contraception

Exclusion criteria

  • Serious organ failure (renal functional impairment, severe central nervous system manifestations, severe heart failure, liver failure)
  • Any clinical evidence of active chronic infection HIV, hepatitis B, hepatitis C
  • Clinical significant pleuritis or pericarditis
  • Type1 Diabetes and/or CROHN's disease
  • Use of Benlysta (belimumab) in the past 4 weeks
  • Use of Rituximab in the past 6 months
  • Vaccination with live attenuated virus in the last month

Treatment and study plan

ILT-101

Drug

Induction phase followed by weekly administrations of ILT-101 on top of SLE background therapy.

SLE background therapy includes ...

Other names: Low dose IL-2

Placebo

Drug

Induction phase followed by weekly administrations of placebo on top of SLE background therapy.

SLE background therapy includes ...

Primary outcomes

  1. SRI-4 (SLE responder index)

    Time frame: at week 12

    Number of participants with SRI-4

Secondary outcomes

  1. Incidence of adverse events

    Time frame: From baseline up to week 24 or 36

  2. Number of participants able to reduce oral steroid dose of 25 and 50%

    Time frame: From baseline to week 12 or 24

  3. Anti ds-DNA by immunology-based assay

    Time frame: From baseline to week 12 or 24

    Change in anti-dsDNA as compared to baseline

  4. %Tregs

    Time frame: From baseline to week 12 or 24

    % change in Tregs as compared to baseline

Sponsors and collaborators

Lead sponsor

Iltoo Pharma

Industry

Registry information

Official study title

A Phase II, Multi-centre, Randomized, Double Blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Pharmacokinetics of ILT-101 in Patients With Active Moderate to Severe Systemic Lupus Erythematosus (SLE)

Acronym: LUPIL-2

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Nov 4, 2016
Registry last updated
Mar 5, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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