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Evaluation the efficacy of Rituximab (Zytux) in diffuse cutaneous Systemic sclerosis treatment

Evaluation the clinical trial of Rituximab (Zytux) efficacy in improving the skin stiffness and lung involvements of the patients with diffuse cutaneous Systemic sclerosis with diffuse skin involvement

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022126686N1
Enrollment
20
Registered
2016-08-12
Start date
2016-07-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic sclerosis (Scleroderma). systemic sclerosis with lung involvementJ99.1*

Interventions

The Zytux which is Rituximab biosimilar with the Iran insurance approval will be administered intravenously with the dosage of 1 gram on the beginning of the treatment, followed by an other 1 gram in
Treatment - Drugs

Sponsors

Aryogen pharmed
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: age more than 20 year old; patients with diffuse cutaneous Systemic sclerosis (SSc) with disease duration less than 7 years from the Raynaud's phenomen; modified Rodnan skin score (mRSS) more than 20; the presence of interstitial lung disease (ILD) in high resolution computed tomography (HRCT) or pulmonary function test (PFT) or both (if the ILD involvement is more than 20% it will be sufficient and in the other situation the ILD should be proved by HRCT and PFT); the mRSS should be remained unchanged after 6 months of the treatment with Endoxan or Cellcept as the previous therapy. Exclusion Criteria: the previous history of Rituximab administration; the history of nervous system disorders like Multiple sclerosis; the history of viral hepatitis like Hepatitis B or C; the history of human immunodeficiency virus infection; the history of tuberculosis infection with PPD more than 5 millimeter; the history of malignancy; dyspnea at rest; the sign and symptoms of congestive heart failure at rest; the history of infectious diseases; the history of cardiac arhythmia on electrocardiogram; the history of prednisolone usage more than 10 mg per day; tricuspid regurgitation jet flow velocity more than 2.8; pulmonary arterial pressure more than 35 according to trans-thoracic ecocardiography; ejection fraction less than 40%; diffusion capacity of the lung for carbon monoxide less than 50%; forced vital capacity less than 50%; serum creatinine level more than 1.5; the history of scleroderma renal crisis; the history of co-morbid cardiac, pulmonary and renal diseases unrelated to SSc.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Skin stiffness (modified Rodnan skin score). Timepoint: Before and after 6 months of treatment. Method of measurement: The examination by fixed Rheumatologist.;Lung involvement according to ground glass opacities and lung fibrosis. Timepoint: Before and after 6 months of treatment. Method of measurement: Spirometery, diffusion capacity of the lungs for carbon monoxide, high resolution computed tomography.

Secondary

MeasureTime frame
The side effects of the biosimilar drug, Zytux. Timepoint: Three and six months after treatment if any side effect will present. Method of measurement: Clinical and laboratory examination and diagnosis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKourosh Sheikh Ahmadi

Rheumatology research center

maadarya@yahoo.com+98 21 8822 0065

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026