Pharmacokinetics of Vitamin D in Multiple Sclerosis and in Health



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - 60
Updated:3/7/2019
Start Date:November 2010
End Date:March 2014

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Pharmacodynamic and Immunologic Effects of Vitamin D Supplementation in Patients With Multiple Sclerosis and Healthy Controls

This is a pilot study of oral vitamin D supplementation to determine if patients with
Multiple Sclerosis (MS) and healthy individuals attain a similar increase in serum
25-hydroxyvitamin D levels. The investigators will also assess whether the immunologic or
relevant gene expression response to oral vitamin D supplementation differs in patients with
MS and healthy controls.


Inclusion Criteria:

- Female

- Healthy or multiple sclerosis

- Aged 18 to 60

- Body mass index is between 18 kg/m2 and 30 kg/m2

- Screening 25-hydroxyvitamin D level ≤ 75 nmol/L (30 ng/mL)

- White race

- Non-Hispanic ethnicity

- Willing to use birth control during study

- Willing to not use tanning bed during study

If subject has multiple sclerosis:

- Relapsing-remitting MS, as defined by McDonald 2005 criteria

- Screening Expanded Disability Status Scale score ≤ 3.0

- Using no medication for MS, or taking Copaxone, (glatiramer acetate), interferons, or
natalizumab

Exclusion Criteria:

- Pregnant or nursing

- Taking multivitamin & unwilling to remain off it during study

- Taking cod liver oil & unwilling to remain off it during study

- On a fat-restricted diet

- History of renal disease or nephrolithiasis (kidney stones)

- History of liver disease

- Taking thiazide diuretics

- History of hyperthyroidism

- History of infection with Mycobacterium species

- History of sarcoidosis

- History of cancer

- History of cardiac disease

- History of HIV

- History of gastrointestinal disorder

- Taking medications that interfere with gastrointestinal absorption

- Cigarette smoker in past month

- Use of illicit drugs in past month

- Use of steroids in past month

- History of hypercalcemia, and screening serum calcium ≤ 10 mg/dL (UCSF) or ≤ 10.7
mg/dL (Johns Hopkins)

- History of hypercalciuria

- Evidence of anemia (Hgb <11.0 g/dL)

- History of other serious medical conditions

- Taking medications that involve the P450 system or may interact with vitamin D
(digoxin, diltiazem, verapamil, cimetidine, heparin, or low-molecular weight heparin)

- Other concerns about safety from the perspective of the treating physician

If subject has MS:

-History of major heat sensitivity (leading to sun-avoidant behaviors)
We found this trial at
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San Francisco, California 94143
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3400 N Charles St
Baltimore, Maryland 21205
410-516-8000
Johns Hopkins University The Johns Hopkins University opened in 1876, with the inauguration of its...
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