Chloroquine to Treat People With Metabolic Syndrome Aim2 (ARCH-MS)

• Status: Active, not recruiting
• Trial end date: 2020-12-01
• Target enrollment: 0
• Participant gender: All

Summary

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the short-term effectiveness of chloroquine, a protein-activation medication, at improving metabolic syndrome.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Washington University School of Medicine
• Collaborator: National Heart, Lung, and Blood Institute (NHLBI)
• Treatments: Chloroquine; Chloroquine diphosphate

Criteria

Inclusion Criteria:

• Diagnosis of metabolic syndrome, as determined by at least three of the following five criteria:

1. Elevated fasting triglyceride levels greater than or equal to 150 mg/dL

2. Low HDL cholesterol levels: less than 50 mg/dL for women and less than 40 mg/dL for men

3. Hypertension (=>130/85 mm Hg =<160/100 mm Hg) untreated; or hypertension controlled (=<150/90 mm Hg) on a stable medication regimen for 4 weeks prior to baseline visit.

4. Increased waist circumference: greater than 35 inches in women and greater than 40 inches in men

5. Elevated fasting glucose levels =<100 mg/dL but =>126 mg/dL

• Subjects may be on a stable doses of a statin drug for at least 3 months

• Subjects may be on a stable doses of L-thyroxine for at least 3 months

• Willing to use acceptable form of birth control (e.g., hormonal birth control, double barrier methods)

Exclusion Criteria:

• Prior travel treatment with chloroquine or hydroxychloroquine as follows:

1. any exposure in the past 2 years,

2. >30 days of therapy if exposure was between 2 and 5 years ago,

3. >90 days of therapy if exposure was between 5 and 10 years ago,

4. >6 months of therapy if exposure was 10 to 20 years ago,

5. >1 year of therapy if exposure was 20 to 30 years ago,

6. No limit if last exposure was >30 years ago, ex. during the Vietnam conflict.

• Morbid obesity (body mass index [BMI] greater than 45)

• Coronary artery disease or other vascular disease

• History of stroke

• Chronic kidney insufficiency (i.e.,estimated glomerular filtration rate (eGFR) less than 60 ml/min/1.73m2)

• Diabetes

• Seizure disorder

• History of psoriasis

• Blood disorders, including anemia (i.e., hemoglobin levels less than 13 g/dL in men and less than 12 g/dL in women)

• Current malignancy or active treatment for recurrence prevention, example tamoxifen. Cancer considered to be cured, either as a result of surgery or other treatment is not exclusionary.

• Asthma requiring daily beta agonist therapy or intermittent oral steroids is exclusionary. Inhaled steroids are acceptable. Obstructive sleep apnea will be allowed if Continuous Positive Airway Pressure (CPAP) or other therapy has been stable for 6 months. Other active respiratory diseases are excluded.

• Liver disease, or liver function test results greater than twice the normal value

• Active infection, including HIV

• Serious illness requiring ongoing medical care or medication

• Treatment with atypical anti-psychotic medication. Treatment with any other medication for psychiatric illness, unless on a stable dose for 6 weeks prior to enrollment. Patients with unstable psychiatric disorders are excluded per the decision of the study MD regardless of medication history.

• Taking any of the following lipid lowering medications: niacin, fibrates, and greater than 1 gm fish oils

• Uncontrolled hypertension (BP >150/90) at enrollment.

• Need for daily over the counter medications, or currently taking cimetidine or >1000 IU vitamin E daily and unwilling to reduce or discontinue the use of vitamin E or discontinue cimetidine for the duration of the study. Persons taking >1000 IU of vitamin E should reduce the dose 30 days prior to randomization.

• Pregnant, breastfeeding, or intending to become pregnant

• Glucose-6-phosphate dehydrogenase (G6PD) deficiency

• Retinal disease (in particular, drusen or pigmentary changes at the macula); any ocular disease that interferes with the eye examination (e.g., cataracts)

• Auditory disease or hearing loss; persons with total, irreversible hearing loss can be enrolled.

• Participation in another clinical trial within past 30 days prior to screening and 60 days prior to randomization. Questionnaire or observational studies are not exclusionary.