17,261 trials
Major Depressive Disorder
Primary: Recall of Cognitive Therapy Content — 25.4; 26.8; 24.7; 28.2 Number of correct units of information
Leukemia · Myelodysplastic Syndromes
Primary: PHASE I: Maximum Tolerated Dose of Azacitidine — 75 mg/m2 subcutaneously for 5 days
Leukemia
Primary: Overall Response Rate — 23; 31; 23 Participants
Chronic Hepatitis B
Primary: Proportion of Patients With HBsAg Response at 12 Week of Therapy — 0; 0; 1; 0 Participants
Influenza
Primary: Number of Participants With Adverse Events — 5; 8; 69; 30 Participants
HIV/AIDS · Clinical Depression
Primary: Insomnia Severity Index (ISI) — 11 score on a scale
Breast Cancer · HER2-negative Breast Cancer
Primary: Pathologic Complete Response Rate (ypCR) Following Neoadjuvant Therapy in Breast and Axillary Lymph Nodes — 26.3; 16.7 percentage of participants
Chronic Lymphocytic Leukemia · Stage 0 Chronic Lymphocytic Leukemia · Stage I Chronic Lymphocytic Leukemia
Primary: Arm A: Percentage of Complete Responses — 46 percentage of participants
Acne Vulgaris
Primary: Percent Change From Baseline to Week 12 in the Inflammatory (Papules and Pustules) Lesion Counts on the Face — -60.84; -62.17 percentage change in lesion counts — p=0.5947
Pheochromocytoma · Paraganglioma
Primary: Number of Patients With Complete (CR), Partial (PR), or Minor (MR) Response and Without Progressive Disease — 28 Participants
HIV Infection
Primary: Number of Participants With at Least One Side Effect, Adverse Event, and Serious Adverse Event — 20; 17; 12; 11 Participants
Infections, Papillomavirus
Primary: Number of Seroconverted Subjects for Anti-HPV-16 and Anti-HPV-18 — 163; 1; 150; 2 Participants
Irritable Bowel Syndrome Characterized by Constipation
Primary: Change From Baseline in Weekly CSBMs Frequency Over the 12-Week Treatment Period (mITT Population) — 1.28; 2.12; 2.74; 2.44 CSBMs per week
Traumatic Brain Injury
Primary: Disability Rating Scale — 12.5; 9.7; 8.5; 6.0 units on a scale — p=0.021
Tuberculosis
Primary: Number of Subjects With Grade 3 Solicited Local Symptoms — 1; 0; 1; 0 Participants