12,372 trials
Type 1 Diabetes
Primary: Mean Weekly Blood Glucose — 187; 178 mg/dL
Breast Cancer · Neutropenia
Primary: Duration of Grade 3 or 4 Neutropenia (ANC <1.0×10^9/L) in Cycle 1 — 0.68; 0.71 days
Primary Hypercholesterolemia or Mixed Dyslipidemia
Primary: Percentage Change in Low-density Lipoprotein Cholesterol (LDL-C) (mg/dL) From Baseline at Day 150 - Core Analysis: Core Part — -45.87; 1.62 % change in LDL-C — p=<0.0001
COPD
Primary: The Proportion of CAT Score Responders in the Full Analysis Set at Week 12 — 12 Participants
Anemia
Primary: Incidence of Treatment-emergent Adverse Events During Each 7-day Study Period — 174; 114 participants
Actinic Keratosis · Warts · Basal Cell Carcinoma
Primary: Number of Accumulated New Skin Lesions at Month 3 — 65; 103 new skin lesions — p=0.0120
Generalized Myasthenia Gravis
Primary: Percentage of Participants With Treatment-emergent Adverse Events (TEAEs) — 78.4; 94.1 percentage of participants
Chronic Lymphocytic Leukemia (CLL)
Primary: Minimal Residual Disease (MRD) Response Rate Measured in Peripheral Blood (PB) Using Next Generation Sequencing (NGS) — 81.3; 54.7 percentage of participants — p=0.0004
Insomnia
Primary: Sleep Diary Sleep Efficiency — 73.2; 72.5; 72.9; 84.5 Percentage Total Sleep Time/Time in Bed
Prostatic Neoplasms · Prostatic Neoplasms, Castration-Resistant
Primary: Sensitivity of Ga 68-labeled PSMA-11 Positron Emission Tomography/Computed Tomography (PET/CT) for the Detection on a Per Patient Basis — 1.0 proportion of participants
Axial Spondyloarthritis
Primary: Percentage of Patients Achieving an ASAS40 Response at Week 24 — 40.1; 49.2 Percentage of participants — p=0.119
Migraine
Primary: Mean Change From Baseline in Monthly Average Number of Migraine Days During 12-Week Period After the First Dose of Study Drug — -1.4; -2.5 days/month — p=0.0210
HIV
Primary: Bacterial Gene Richness (Observed Unique Genes). Analysis of the Composition, Structure and Function of the Intestinal Microbiome. * — 768358; 730732; 767756; 808911…
Multiple Myeloma
Primary: Post-Consolidation Stringent Complete Response (sCR) Rate — 110; 157 Participants — p=0.0010
Carcinoma, Non-Small-Cell Lung
Primary: Number of Patients With Adverse Events According to Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0 — 478 Participants