65,437 trials
Glaucoma
Primary: Mean Change From Baseline in Diurnal IOP at Week 6
Osteoporosis
Primary: Number of Participants With Adverse Events — 7; 6; 0; 1 Participants
Healthy Volunteers · Hypercholesterolemia
Primary: Number of Participants With One or More Other Non-Serious Adverse Events (AEs) or Any Serious AEs (SAEs) — 3; 1; 0; 0 Participants
Laparoscopic Colectomy
Primary: Medical Recovery (Defined as Pain Sufficient Controlled by Oral Analgesia, Fully Mobile Patients or at Least as Mobile as at Admission and Tolerance of the Patient of…
Lung Cancer
Primary: Determine Feasibility as Measured by Rates of Recruitment. — 66 percentage of participants
HIV-1 Infection
Primary: The Proportion of Patients Who Can Achieve of Less Than 20 HIV RNA Copies Per ml at Week 48 of Both Arms. — 41; 36 Participants
Type 2 Diabetes Mellitus
Primary: Change From Baseline in A1C at Week 30 — -1.88; -1.42 Percent A1C — p=< 0.001
Actinic Keratosis
Primary: Number of Participants With Adverse Events — 12; 11; 6; 3 Participants
Healthy Subjects
Primary: Maximum Observed Plasma Concentration (Cmax) of Guaifenesin — 1066.11; 1117.31 ng/ml
Healthy Subjects
Primary: Maximum Observed Plasma Concentration (Cmax) of Guaifenesin — 1730; 1230; 1110 ng/mL
Human Immunodeficiency Virus-1 (HIV-1)
Primary: Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of MK-1439 Following a Single Administration of MK-1439 — 28.6; 31.9; 35.5; 29.1 µM*h
Psoriatic Arthritis
Primary: Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 24 — 50.7; 60.9; 65.0 percentage of participants — p=0.005
Prostate Cancer
Primary: Pharmocodynamically Optimal Dose (POD) of Rapamycin as Determined by Number of Participants With Greater Than or Equal to 60% Tumor S6 Kinase Inhibition by…
PTSD
Primary: Number of Participants With VA Mental Health Care Engagement — 40; 30; 28; 28 Participants — p=0.1996
Colorectal Cancer · Colorectal Neoplasms · Colorectal Carcinoma
Primary: Count of Participants With Serious and Non-serious Adverse Events Assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0) — 6; 9 Participants