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OpenTrials
Active, Not Recruiting

NCT Number: NCT04206644

Systemic Sclerosis and Jak Inhibitors : Emphasis on Macrophages

The Sclero-JAK project aims to assess the impact of a JAK1/2 inhibitor (ruxolitinib) on activation states of monocytes-derived macrophages (MDM) from systemic sclerosis (SSc) patients

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Rennes University Hospital

Rennes, 35033, France

About this study

Systemic sclerosis is a fibrotic and inflammatory chronic autoimmune disorder with no disease modifiying drug available to date. JAK inhibitors may represent a relevant therapeutic candidate for this disease;

The primary objective of this study is to characterize the impact of Ruxolitinib (a JAK ½ inhibitor) on the prof-fibrotic properties of MDM from SSc patients in vitro.

The primary outcome will be the concentration of CCL18 evaluate by ELISA in the condition media of MDM from SSc patients pre treated or not in vitro by ruxolitinib.

The secondary objectives :

  • To characterize the impact of ruxolitinib on other pro-inflammatory or pro-fibrotic cytokines
  • To characterize the impact of ruxolitinib on membrane expression of macrophagic polarization markers of MDM from SSc patients
  • To evaluate the impact of ruxolitinib on the phenotype of MDM from healthy donors exposed in vitro to the serum of SSc patients.
  • To determine the variability of the effects of ruxolitinib on MDM of SSc patients depending on key clinical characteristics (diffuse versus limited SSc, patients with or without Interstitial Lung disease ILD)

The secondary outcomes :

  • ELISA of the following cytokine evaluated in the condition media of SSc MDM pre-treated or not with ruxolitinib : PDGFbb, IL-6, CXCL10, CXCL4
  • Membrane expression (flow cytometry) of the following markers expressed by SSc MDM pre-treated or not with ruxoltinib : CD204, CD206, CD163, CD86, CMHII, TLR4.
  • Evaluation of the same cytokines and membrane markers in MDM from HD exposed to serum media of SSc patients.
  • Variation of the effect of ruxolitinib on the primary outcome (CCL18 secreted in the condition media of MDM from SSc patients) in sub groups depending on the following characteristics :
  • Auto antibodies (anticentromere, antitopoisomerase, anti RNA polymerase III or none)
  • modified Rodnan skin score
  • Digital ulcers (current or past)
  • Pulmonary involvement (Interstitial Lung disease on CT scan)
  • Heart involvement (Pulmonary arterial hypertension on echocardiography)

Who can participate

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

Inclusion criteria

  • patients with systemic sclerosis according to the ACR/EULAR 2013 classification criteria for systemic sclerosis or Patients with systemic lupus according to the ACR2019 classification criteria for systemic lupus
  • with informed consent for participation to the study

Exclusion criteria

  • patients unable to consent
  • patients with anemia inferior to 7g/dL

Treatment and study plan

Biological analysis

Other

biological analysis of the Concentration of CCL18

Primary outcomes

  1. Concentration of CCL18 in the condition media of MDM from SSc patients

    Time frame: through study completion, an average of 4 year

    at the end of the study

Sponsors and collaborators

Lead sponsor

Rennes University Hospital

Other

Registry information

Acronym: SCLERO JAK

Important dates

Study start
2021
Primary completion
2023
Study completion
2027
First posted
Dec 20, 2019
Registry last updated
Apr 12, 2023

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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