Recruiting
Phase 2

Mycophenolate Mofetil

Sponsor:

Centre hospitalier de l'Université de Montréal (CHUM)

Code:

NCT05785065

Conditions

Systemic Sclerosis With Lung Involvement

Systemic Sclerosis

Interstitial Lung Disease

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Mycophenolate Mofetil

Placebo

Study Details

Brief summary:

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.

Conditions

Systemic Sclerosis With Lung Involvement

Systemic Sclerosis

Interstitial Lung Disease

Study ID

NCT05785065

Start date

Aug 29, 2024

Status verified date

Apr, 2025

Completion date

Dec, 2028

Anticipated

Primary completion date

Dec, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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 before screening, that shows fibrosis affecting less than 20% of the lungs, as confirmed by an expert radiologist;
5. Diagnosis of ILD within 7 years before screening;
6. Forced vital capacity of 80% predicted and above, on pulmonary function tests obtained within 6 months before screening;
7. Able to communicate in French or English;

Exclusion Criteria:

1. Progressive pulmonary fibrosis, defined as at least two of three criteria (worsening symptoms, radiological progression, and physiological progression) occurring within the past year with no alternative explanation, as defined by the 2022 ATS/ERS/JRS/ALAT Clinical Practice Guideline;
2. Use of medications with putative lung disease-modifying properties:

1. Current use of MMF, mycophenolic acid, azathioprine, calcineurin inhibitors (e.g. tacrolimus, cyclosporin A), tocilizumab, nintedanib, pirfenidone or corticosteroids (Prednisone equivalent dose >10 mg/day) at time of screening
2. Cyclophosphamide within one year prior to screening
3. Rituximab within 6 months prior to screening
4. Cell therapies (including stem cell transplantation) within one year prior to screening
3. Current use of other biological, targeted synthetic or investigational products with immunosuppressive effects (e.g. TNF inhibitors, abatacept, tofacitinib) at time of screening
4. Any contraindication to MMF, including:

1. Pregnancy and/or breastfeeding
2. Female of childbearing potential not using reliable method of contraception
3. Persistent leucopenia (white blood cell count <3.0 x103/μL)
4. Persistent thrombocytopenia (platelet count <100 x103/μL)
5. Persistent anemia (hemoglobin <100 g/L)
6. Baseline liver enzymes (alanine transaminase (ALT) or aspartate transaminase (AST)) or bilirubin >1.5 times the upper limit of normal, other than due to Gilbert's disease
7. Uncontrolled congestive heart failure
8. Active infection (lung or elsewhere)
9. Active solid or hematological malignancy (other than basal cell cancer of the skin or cervical carcinoma in situ removed entirely by biopsy)
10. Active peptic ulcer disease
11. Other serious concomitant medical illness, unreliability or drug abuse that might compromise the patient's ability to safely take MMF
12. Use of drugs or products with significant interactions with MMF

Study Design

Enrollment

35 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: Mycophenolate mofetil

2 to 4 capsules of mycophenolate mofetil twice daily.

placebo comparator: Placebo

2 to 4 capsules of placebo twice daily.

Interventions

Mycophenolate Mofetil

The participant will receive 500 mg to 1000 mg twice daily of mycophenolate mofetil administered orally for 96 weeks.

The dose scheduling will be as follow:

Weeks 1 and 2: 500 mg twice a day Weeks 3 and 4: 750 mg twice a day Weeks 5 to 96: 1000 mg twice a day

Placebo

The participant will receive 500 mg to 1000 mg twice daily of placebo administered orally for 96 weeks.

The dose scheduling will be as follow:

Weeks 1 and 2: 500 mg twice a day Weeks 3 and 4: 750 mg twice a day Weeks 5 to 96: 1000 mg twice a day

Primary outcome measure

  • Total number of potentially eligible patients identified per site [ Time Frame: Over one year ]
  • Proportion of potentially eligible patients who provide consent per site [ Time Frame: Over one year ]
  • Proportion of consented participants who meet the eligibility criteria per site [ Time Frame: Over one year ]
  • Monthly rate of randomized participants per site [ Time Frame: Over one year ]
  • Adherence to treatment as assessed by Participant Dosing Diaries [ Time Frame: From the first dose to the last dose taken for each participant, up to 96 weeks ]
  • Drug adherence rate as assessed by Pharmacy Accountability Logs [ Time Frame: From the first dose to the last dose taken for each participant, up to 96 weeks ]
  • Adherence to the study protocol as assessed by the number of protocol deviations [ Time Frame: Over total study period (up to 96 weeks per participant) ]
  • Proportion of participants intolerant to the study drug who discontinue trial treatment [ Time Frame: Over total study period (up to 96 weeks per participant) ]
  • Proportion of participants receiving the allocated treatment at 48 weeks [ Time Frame: At 48 weeks ]
  • Proportion of participants receiving the allocated treatment at 96 weeks [ Time Frame: At 96 weeks ]
  • Proportion of participants with complete primary efficacy outcome data at 48 weeks [ Time Frame: At 48 weeks ]
  • Proportion of participants with complete primary efficacy outcome data at 96 weeks [ Time Frame: At 96 weeks ]
  • Proportion of participants lost to follow-up [ Time Frame: Over total study period (up to 96 weeks per participant) ]

Central Contacts and Locations

Central contacts

Unité d'innovation thérapeutique, CHUM

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

Locations

Centre hospitalier de l'Université de Montréal (CHUM)

Recruiting

Montreal, Quebec, Canada, H2X 3E4

Contacts

Unité d'innovation thérapeutique, CHUM

5148908000uit.eligibilite.chum@ssss.gouv.qc.ca

Principal Investigator:

Sabrina Hoa, MD MSc

More Information

Sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Last update posted

Apr 11, 2025

Last verified

Apr, 2025

Keywords

  • Systemic sclerosis
  • Mycophenolate mofetil
  • Interstitial lung disease

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Centre hospitalier de l'Université de Montréal (CHUM) on 2025-04-11.