Actively Recruiting
Effects of Stopping Hydroxychloroquine in Elderly Lupus Disease
Led by NYU Langone Health · Updated on 2026-02-25
330
Participants Needed
10
Research Sites
261 weeks
Total Duration
On this page
Sponsors
N
NYU Langone Health
Lead Sponsor
N
National Institutes of Health (NIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Hydroxychloroquine (HCQ) is a systemic lupus erythematosus (SLE) medication that has been very effective in reducing lupus disease activity and keeping patients stable with reduced symptoms. Despite a track record of safety with regard to infection compared to traditional immunosuppressive agents, the risk of HCQ retinal toxicity escalates with continued use. Evaluation using sensitive standard of care approaches suggests nearly a third of patients accrue retinal damage. Data are needed to accurately weigh the balance between accumulating ocular exposure of HCQ versus the risk of disease flare in a population that may have more inactive disease than younger patients. The purpose of this trial is to address the safety of withdrawal of HCQ in SLE patients =60 years old. The central hypothesis is that HCQ can be safely discontinued in stable/quiescent patients assessed by validated disease activity and flare instruments in the context of serologic, cytokine and transcriptomic profiling. Patients will be randomized to either the placebo or active arm and followed every 2 months for one year to assess disease activity and flares.
CONDITIONS
Official Title
Effects of Stopping Hydroxychloroquine in Elderly Lupus Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form provided
- Willingness to follow all study procedures and be available for the study duration
- Age 60 years or older at enrollment
- Normal optical coherence tomography and visual field assessment within 6 months before screening
- Ability to take oral medication
- Established systemic lupus erythematosus diagnosed at least 7 years ago meeting criteria
- Stable disease with DORIS remission at screening, including Clinical SLEDAI=0, SELENA-SLEDAI PGA 2 0.5, and prednisone dose 2 5 mg daily
- No moderate or severe lupus flares in the year before screening
- Taking 200 mg or more of hydroxychloroquine daily for at least 7 years
You will not qualify if you...
- Not meeting stable disease status by DORIS criteria
- Evidence of retinopathy in eye exams
- Clinical SLEDAI score greater than 0
- Taking more than 5 mg/day prednisone
- Using immunosuppressive or biological drugs
- Any concern from rheumatologist about lupus activity not captured by SLEDAI
- Hydroxychloroquine blood level below 100 ng/ml
- Unable or unwilling to comply with study procedures
- Diagnosed dementia or cognitive impairment, including stroke-related cognitive issues
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 10 locations
1
University of California, Los Angeles
Los Angeles, California, United States, 90095
Actively Recruiting
2
Hackensack Meridian Health
Hackensack, New Jersey, United States, 07601
Actively Recruiting
3
VA NY Harbor Healthcare System
New York, New York, United States, 10010
Actively Recruiting
4
NYC Health + Hospitals/Bellevue
New York, New York, United States, 10016
Actively Recruiting
5
NYU Langone Health
New York, New York, United States, 10016
Actively Recruiting
6
Hospital for Special Surgery
New York, New York, United States, 10021
Actively Recruiting
7
Columbia University Irving Medical Center/New York Presbyterian
New York, New York, United States, 10032
Actively Recruiting
8
Montefiore Medical Center/Albert Einstein College of Medicine
The Bronx, New York, United States, 10461
Actively Recruiting
9
Oklahoma Medical Research Foundation
Oklahoma City, Oklahoma, United States, 73104
Actively Recruiting
10
Penn State MS Hershey Medical Center
Hershey, Pennsylvania, United States, 17033
Actively Recruiting
Research Team
M
Mala Masson
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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