Non-infectious Intermediate and Posterior Uveitis Clinical Trial
Official title:
Combination Daclizumab/Denileukin Diftitox (Ontak) Therapy for the Induction of Immune Tolerance in Non-infectious Intermediate and Posterior Uveitis
This study will determine whether treatment with a combination of the drugs daclizumab and
denileukin diftitox can eliminate the need for long-term daclizumab treatment in adult
patients with uveitis. Denileukin diftitox kills white blood cells called lymphocytes that
cause inflammation and may be the cause of uveitis.
Patients 18 years of age and older with uveitis in one or both eyes who are on daclizumab
therapy and have not had a disease flareup in 6 months may be eligible for this study.
Candidates are screened with a medical history, physical examination, eye examination
(including vision test, examination of the front of the eye, and pupil dilation for
examination of the retina at the back of the eye), blood tests and a questionnaire about
their vision and daily activities.
After screening, participants undergo the following procedures:
- Daclizumab/ denileukin diftitox treatment. Patients receive their regular dose of
daclizumab intravenously (through a vein). The interval between doses is increased by 1
week after each dose. When the doses are 10 weeks apart, the daclizumab is stopped.
Patients who experience a flare or uveitis are treated with intravenous denileukin
diftitox and possibly local injections of steroids around the eye or increasing or
adding other medicines as needed to control the uveitis.
- Fluorescein angiography to look for blood vessel abnormalities in the eyes. A yellow dye
is injected into an arm vein and travels to the blood vessels in the eyes. Pictures of
the retina (the back portion of the eye) are taken with a special camera that flashes a
blue light into the eye. The pictures show if any dye has leaked from the vessels into
the retina, indicating possible abnormalities.
- Ultrasound and urine tests at enrollment and after 1 year to check kidneys, lymph nodes
and pelvic area.
- Blood tests at enrollment and every 3-6 months for laboratory and immunology tests and
other research tests on blood cells to examine the immune response.
- Follow-up visits approximately every 6 weeks for 2 years for repeat examinations to
determine the response to treatment and drug side effects.
We propose to investigate the possible efficacy of combination daclizumab and denileukin diftitox therapy to induce peripheral immune tolerance in participants presenting with non-infectious intermediate and posterior uveitis. This will be performed using a Phase I/II pilot study. Subjects whose disease is controlled on daclizumab therapy will have their daclizumab-dosing interval progressively increased by one-week increments. If and when they experience signs or symptoms of an ocular flare, they will be treated with denileukin diftitox, 24 hours after which they will receive their usual dose of daclizumab. Participants may receive up to 12 such cycles of daclizumab/denileukin diftitox therapy. When the daclizumab-dosing interval is 10 weeks long or less than 10% of their CD4 T cell CD25 is occupied by daclizumab, therapy will be discontinued. Following discontinuation of daclizumab patients will be followed for recurrence of ocular disease. Failure to reach this study point after 12 cycles or disease recurrence following discontinuation of therapy will constitute a study failure. The primary outcome will be the ability of the participant to be successfully tapered off daclizumab while their disease remains quiet (vitreous haze less than or equal to Trace) at week 104 while receiving no concomitant systemic immunosuppressive medications. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT01314417 -
Treatment of Non-infectious Intermediate and Posterior Uveitis Associated Macular Edema With Intravitreal Methotrexate
|
Phase 1/Phase 2 |