The purpose of this research study is to evaluate the safety and effectiveness of an investigational, extended-release formulation of Febuxostat, 40 mg and 80 mg tablets, compared to the marketed immediate-release formulation of Febuxostat, 40 mg and 80 mg tablets, and a placebo (an inactive substance) in subjects with gout.
The purpose of this study is to evaluate the safety and effectiveness of an investigational topical testosterone gel treatment to see if it can improve testosterone levels in men ages 18 to 80 who have low testosterone.
The purpose of this study is to evaluate the safety and effectiveness of a combination drug consisting of desmopressin and tolterodine compared to tolterodine alone in the treatment of overactive bladder with nocturia in women.
Irritable Bowel Syndrome with Diarrhea (IBS-D) in Women
January 28, 2014
The purpose of this study is to evaluate the effectiveness of an investigational medication compared to a placebo in relieving IBS-D symptoms in female patients 18 years of age or older over a 12-week period.
(Above: Scanning electron microscope image of Vibrio Cholerae bacteria, which infect the digestive system)
The purpose of these two studies is to evaluate the safety and immunogenicity of a single-dose of an investigational oral cholera vaccine compared to a placebo in healthy adults ages 18 to 45 years old and 46 to…
The purpose of this study is to determine whether the administration of an investigational medication in people 65 years of age or older who have unexplained anemia will improve their hemoglobin level over a six-month treatment period.
The purpose of this study is to confirm the effectiveness of single-ingredient pseudoephedrine compared to placebo in children 6 to 11 years old for the temporary relief of nasal congestion due to the common cold.