The purpose of this study is to evaluate the effectiveness of NGX267 in the improvement of decreased salivary flow associated with primary or secondary Sjögren's syndrome. For each patient, the study includes four periods of treatment separated by a washout period that may range from 4 - 8 days according to patient and site discretion. Each treatment period includes two overnight stays in the clinic. One dose of study drug is taken during each treatment period
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
24
Altoona Center for Clinical Research
Duncansville, Pennsylvania, United States
Penn Rheumatology Associates and Sjogren's Syndrome Center
Philadelphia, Pennsylvania, United States
Walter F. Chase MD PA
Austin, Texas, United States
Quantitative and qualitative assessment of dry mouth
Time frame: 36 days
Tolerability and safety of NGX267
Time frame: 36 days
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2 capsules in the am of each treatment period