Actively Recruiting

Phase 3
Age: 60Years +
All Genders
NCT05799378

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

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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