Mycophenolate Mofetil in Systemic Sclerosis With Subclinical Interstitial Lung Disease

Recruiting Phase 2 Interventional Study
Systemic Sclerosis With Lung Involvement Systemic Sclerosis Interstitial Lung Disease
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Other
Participants needed
35 (estimated)
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) · Other
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About This Trial

The goal of this pilot study is to assess the feasibility of a larger study on the efficacy of mycophenolate mofetil in people diagnosed with systemic sclerosis with mild lung involvement. Participants will be recruited over 12 months at 3 academic centers and assigned randomly to receive either mycophenolate mofetil or placebo, a look-alike substance that contains no active drug, for 96 weeks.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Able and willing to provide informed consent and adhere to study protocol; 2. Women and men of all race/ethnicity, aged 18 years and older; 3. SSc based on 2013 ACR-EULAR classification criteria; 4. Presence of interstitial lung disease on HRCT scan, obtained within 12 months…
Contacts

Sabrina Hoa, MD MSc

514-890-8000

sabrina.anh-tu.hoa.med@ssss.gouv.qc.ca

CONTACT

Unité d'innovation thérapeutique, CHUM

uit.eligibilite.chum@ssss.gouv.qc.ca

CONTACT