"Clinical Trial to Determine the Efficacy of Vitamin D for Acne Therapy"

This study will be a randomized, double-blinded, parallel group comparison of calcipotriene
vs. placebo cream. Patients with acne will use calcipotriene or placebo cream 2x/day for 12
weeks and will be assessed at weeks 0, 2, 4, 8 and 12. Each group will have 24 subjects as
calculated by power analysis. Three additional subjects for each group will be recruited
for possible dropouts and total of 27 subjects will be recruited for each group. Primary
endpoint (lesion count) and secondary endpoints described in aims 3.2-3.4 will be
determined. Lesion counts will be assessed by one of the investigator physicians or nurse
practitioner. Adverse effects including irritation, dry skin, inflammation and worsening of
the lesions will be noted at each visit. Photographs will be taken to aid in assessing the
clinical changes.

Inclusion Criteria:

1. Age 18 years or older, of either gender and any racial/ethnic group

2. Subjects must have clinically evident mild to moderate acne vulgaris of the facial
area, IGA scale, grade 2-4

3. Subjects must understand and sign the informed consent prior to participation

4. Subjects must be in generally good health

5. Subjects must be able and willing to comply with the requirements of the protocol

Exclusion Criteria:

1. Oral retinoid use within twelve months of entry into the study

2. Systemic acne therapies (oral antibiotics) within 30 days of entry into the study

3. Topical acne therapies (retinoids, antibiotics) within 14 days of entry into the
study

4. Non-compliant patients

5. Pregnant or nursing women

6. Subjects with a significant medical history or concurrent condition that the
investigator(s) feel is not safe for study participation

7. Subjects with hypercalcemia (hyperparathyroidism, kidney disease)

8. Subjects who cannot avoid excessive exposure to either natural or artificial
sunlight.