Overview

Studies of the Ocular Complications of AIDS (SOCA)--Monoclonal Antibody CMV Retinitis Trial (MACRT)

Status:
Completed
Trial end date:
1996-08-01
Target enrollment:
0
Participant gender:
All
Summary
To evaluate the efficacy and safety of a human anti-CMV monoclonal antibody, MSL-109, as adjunct therapy for controlling CMV retinitis.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Johns Hopkins Bloomberg School of Public Health
Treatments:
Antibodies
Antibodies, Monoclonal
Immunoglobulins
Criteria
Inclusion criteria:

- 13 years or older at entry

- Diagnosis of AIDS according to the Centers for Disease Control and Prevention (CDC)
definition

- Diagnosis of active CMV retinitis as determined by a SOCA-certified ophthalmologist at
time of enrollment

- At least one lesion whose size is one-quarter or more optic disc area

- Currently receiving (for relapsed patients) or scheduled to receive (for newly
diagnosed patients) drugs for primary treatment of CMV retinitis that are not
contraindicated for use with MSL-109

- Visual acuity, in at least one eye that meets other eligibility criteria, of 3 or more
letters on ETDRS chart at 1 meter distance (Snellen equivalent 5/200). Patients with
poorer visual acuity may be enrolled if the visual acuity impairment is possibly
reversible (eg, due to optic disc edema) and vision is at least light perception in
that eye

- Karnofsky score of 60 or more

- Willingness and ability, with the assistance of a caregiver if necessary, to comply
with treatment and follow up procedures

- signed consent statement

Exclusion criteria:

- Current treatment with intravenous immune globulin (IVIG), CMV immune globulin
(CMVIG), alpha-interferon (alpha-IFN), gamma-interferon (gamma-IFN) or interleukin-2
(IL-2)

- Media opacity that precludes visualization of the fundus in all eyes meeting
eligibility criteria

- Active medical problems, including drug or alcohol abuse, that are considered
sufficient to hinder compliance with treatment or follow up procedures

- Retinal detachment, not scheduled for surgical repair, in all eyes meeting other
eligibility criteria