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A Study of MT-0551 in Patients With Systemic Sclerosis

Recruiting
20 - 80 years of age
Both
Phase 3

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Overview

The study will verify the superiority of MT-0551 to placebo at 26 weeks after treatment initiation in systemic sclerosis (SSc) patients using the modified Rodnan Total Skin thickness Score (mRTSS) as a measure of skin thickening. The safety and pharmacokinetics will also be investigated.

Eligibility

Inclusion Criteria:

Additional screening criteria check may apply for qualification:

  1. ACR/European League Against Rheumatism (EULAR) criteria (2013) systemic sclerosis (SSc) diagnostic criteria satisfied.
  2. Skin thickening score based on the mRTSS between 10 and 22 inclusive.

Exclusion Criteria:

Additional screening criteria check may apply for qualification:

  1. Pulmonary hypertension associated with SSc.
  2. Presence of a serious, SSc-related concurrent illness other than interstitial pneumonia.
  3. Finding of inadequate respiratory reserve capacity.
  4. Past history of rituximab, blinatumomab, obinutuzumab, or ofatumumab.
  5. Presence of a clinically significant active infection requiring antimicrobial therapy.
  6. A past history of cancer.
  7. Past history of a recurrent, clinically significant infection.
  8. Past history of severe allergy or anaphylactic reaction to a biologic drug product.
  9. Treatment with live vaccine within a certain period (inactivated vaccine is acceptable).

Study details

Systemic Sclerosis

NCT05198557

Mitsubishi Tanabe Pharma Corporation

27 January 2024

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