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Completed

NCT Number: NCT03209219

Interferon α2a Versus Cyclosporine for Refractory Behçet's Disease Uveitis

Brief summary: This study compares the long-term efficacy and safety of interferon (IFN) α2a and cyclosporine (cyclosporin A, CsA) following suppression of acute attack by high-dose oral glucocorticosteroid in patients with refractory Behçet's uveitis (BDU). Half of the participants will receive IFNα2a while the other half will receive CsA.

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Key information

About this study

Detailed description: Both CsA and IFNα2a have been shown to be effective for long-term control of BDU, however, randomized prospective comparative studies are scarce, particularly in East Asian populations. Our preliminary data gave us the impression that IFNα2a might be more effectiveness than CsA in long-term control of refractory BDU, and this study aimed to compare their effectiveness and safety profiles in a well-designed prospective study. Refractory BDU is defined as relapse of posterior or pan- uveitis with at least 10mg daily prednisone (or equivalent) and one traditional immunomodulatory treatment (IMT) agents. The acute attack is controlled with large dose oral corticosteroid (60mg daily prednisone) for 4 weeks, and then the patients are randomly assigned to the IFN arm and the CsA arm, in which patients are treated with IFNα2a (3×10^6 IU qd for 4 weeks and qod thereafter) and CsA (100mg bid), respectively, along with a fixed tapering regimen of corticosteroid. Patients were followed up until relapse, or for 12 months.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Refractory BDU patients fulfilling the International Criteria for Behçet's disease (ICBD) published in 2013 with recent recurrence of pan- or posterior uveitis;
  • The patient should be on ≥10mg/d oral prednisone or equivalent with at least one of the following IMT agents: cyclophosphamide≥50mg/d, CsA≥100mg/d, azathioprine≥50mg/d, methotrexate≥15mg/w, mycophenolate≥1000mg/d, tacrolimus≥2mg/d.

Exclusion criteria

  • Previous treatment with interferon-α;
  • Pregnancy, breast feeding women;
  • Malignancy;
  • Renal impairment (creatinine > 1.5 mg/dl);
  • Uncontrolled hypertension or diabetes;
  • Depression or other psychic disorders;
  • History of acute or chronic inflammatory joint or autoimmune disease;
  • Patients with severe extra-ocular involvement other than oral/genital ulcer and skin involvement;
  • Organ or bone marrow transplant recipient, cardiac failure > NYHA III;
  • Acute liver disease with ALT or SGPT 2x above normal;
  • White blood cell count < 3500/mm^3;
  • Platelet count < 100000/mm^3;
  • Hgb < 8.5g/dl;
  • T-SPOT TB: ≥200 SFCs per 10^6 PBMC;
  • Active peptic ulcer, systemic or local infection, moderate to severe osteoporosis or other contraindications of large dose corticosteroids;
  • Previous intolerance to CsA;
  • Other severe ocular diseases or intraocular surgery within 3 months;
  • Media opacity precluding a clear view of the fundus;
  • Positive screen test for HBV, HCV, HIV infection or syphilis;
  • Body weight <45 kg;
  • Alcohol abuse or drug abuse;
  • Mental impairment;
  • Uncooperative attitude.

Treatment and study plan

Interferon alfa-2a

Drug

3×10^6 IU, subcutaneous or intramuscular injection, qd for × 4 weeks, and qod thereafter

Cyclosporine Pill

Drug

100mg, oral, bid

Primary outcomes

  1. Response rate

    Time frame: Within the 12-month follow-up period

    Percentage of participants who achieve complete remission or partial remission

  2. Complete remission rate

    Time frame: Within the 12-month follow-up period

    Percentage of participants who achieve complete remission without relapse of posterior or pan-uveitis

  3. Tolerance rate

    Time frame: Within the 12-month follow-up period

    Percentage of participants who adhere to the treatment without severe side effects

Secondary outcomes

  1. Time to reach complete remission

    Time frame: Within the 12-month follow-up period

    The time from the therapy initiation to a complete absence of ocular inflammation for complete responders

  2. Duration of relapse-free

    Time frame: within the 12-month follow-up period

    The duration between the therapy initiation to the relapse for partial responders and nonresponders

  3. BCVA

    Time frame: Within the 12-month follow-up period

    Changes of best-corrected visual acuity

  4. BOS24 score

    Time frame: Within the 12-month follow-up period

    Score of ocular inflammation using the Behcet disease ocular attack score 24 (BOS24)

  5. Glucocorticoid-sparing effect

    Time frame: Within the 12-month follow-up period

    Changes of corticosteroid dosage

  6. Incidence of adverse effects

    Time frame: Within the 12-month follow-up period

    Incidence of adverse effects

  7. Incidence of significant abnormal changes in vital signs or laboratory test results

    Time frame: Within the 12-month follow-up period

    Incidence of significant abnormal changes in vital signs or laboratory test results

  8. Adverse effects profile

    Time frame: Within the 12-month follow-up period

    Types of drug adverse effects

Sponsors and collaborators

Lead sponsor

Peking Union Medical College Hospital

Other

Registry information

Official study title

Randomized Prospective Comparative Study of Interferon α2a and Cyclosporine in Patients With Refractory Behçet's Disease Uveitis

Important dates

Study start
2017
Primary completion
2020
Study completion
2021
First posted
Jul 6, 2017
Registry last updated
Feb 23, 2021

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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