17,261 trials
Alcohol Use Disorder
Primary: Heart Rate — 64.57; 68.36; 66.82; 62.82 BPM — p=0.0563
Breast Cancer
Primary: Percentage of Participants With at Least One Event of New York Heart Association (NYHA) Class III or IV Heart Failure During the Neoadjuvant Treatment Period — 1.5; 0…
Sickle Cell Disease · Priapism
Primary: Greater Than or Equal to a 50% Reduction in Priapic Episodes — 3; 3 Number of participants — p=1
HIV-HCV
Primary: The Percentage of Subjects Who Achieve Sustained Viral Response (SVR12) 12 Weeks After the Stop of Treatment Drugs — 90; 80 Percentage of subjects
Prostate Cancer
Primary: Percentage of Participants With Effective Castration Rate Over 25 Weeks — 95; 89 percentage of participants
Hepatitis B
Primary: Percentage of Participants With Local and Systemic Post-injection Reaction Rates — 38.2; 37.9; 37.2; 33.0 percentage of subjects
Asthma
Primary: Change From Baseline In Trough (Morning Predose And Pre-Rescue Bronchodilator) Forced Expiratory Volume In 1 Second (FEV1) Over The 12-Week Treatment Period — 0.170…
Progressive Supranuclear Palsy
Primary: Adverse Events — 23 Number of Adverse Events
Asthma
Primary: Standardized Baseline-Adjusted Area Under the Curve For Forced Expiratory Volume In 1 Second Over 12 Hours Post-dose (FEV1 AUC0-12) — 52.13; 203.84; 248.98; 279.69 mL…
Alcoholism · Schizophrenia
Primary: Self Reported Weekly Alcohol Consumption — 23.4; 19.6; 15.7; 10.0 percentage of days
Multiple Myeloma
Primary: Overall Response Rate — 6; 1; 20; 43 Participants
Asthma
Primary: Change From Baseline In Trough (Morning Predose And Pre-Rescue Bronchodilator) Forced Expiratory Volume In 1 Second (FEV1) Over The 12-Week Treatment Period — 0.059…
Skin Rash · Lung Cancer
Primary: Frequency of Participants Who Experienced Any Grade of Rash As Characterized By The Common Toxicity Criteria for Adverse Effects (CTCAE) V4.0 — 44.5; 75.5 Percentage of…
Diabetes Mellitus, Type 1
Primary: Insulin Independence. — 2 Participants
Primary Sclerosing Cholangitis (PSC)
Primary: Number of Participants With Treatment-Emergent Adverse Events (TEAEs) — 1; 2; 2; 1 participant