17,261 trials
Obesity · Pre-diabetes
Primary: Change in Adipose Pro-inflammatory T Helper Type 1 Cell Percentages After 3 Months — -1.6 Percentage of CD3+ T cells
Rheumatoid Arthritis
Primary: Change From Baseline on the Disease Activity Score Modified to Include the 28 Diarthrodial Joint Count-High-Sensitivity C-Reactive Protein (DAS28-hsCRP) — -0.99; -1.88…
Marginal Zone B-cell Lymphoma
Primary: Complete Response Rate (CRR) — 73 Percentage of patients
Diabetes type1
Primary: Incidence of Treatment-emergent Adverse Events (TEAE) — 1; 6; 1; 19 Events
Malignant Pleural Mesothelioma · Mesothelioma
Primary: Disease Control Rate (DCR) — 75 percentage of participants
Breast Cancer · Triple Negative Breast Cancer
Primary: Number and Percentage of Participants With Pathologic Complete Response (pCR) Rate — 8 Participants
Lymphangioleiomyomatosis
Primary: Serum Vascular Endothelial Growth Factor-D (VEGF-D) Levels After Treatment With a Combination of Resveratrol and Sirolimus as Compared to Baseline Serum VEGF-D Levels on…
Anosmia · Covid19
Primary: Change in Brief Smell Identification Test (BSIT) — 6.77; 7.20; 7.89; 7.88 score on a scale
Sleep Apnea, Obstructive
Primary: Duration of Obstructive Events — 22.72; 24.66 seconds
SARS-CoV 2
Primary: Cumulative Number of Hospitalizations or Deaths Prior to Hospitalization — 17; 37 Participants — p=0.005
Non-Hodgkin's Lymphoma, Relapsed · Chronic Lymphoid Leukemia in Relapse · Non-Hodgkin's Lymphoma Refractory
Primary: Maximum Tolerated Dose (MTD) — NA 10^6 CAR T cells
Mantle Cell Lymphoma · Lymphoma, Mantle Cell
Primary: Median Progression-free Survival (PFS) in Participants Treated With Etoposide, Prednisone, Vincristine, Cyclophosphamide, Doxorubicin, and Rituximab (EPOCH-R) — 23.5…
Dystrophic Epidermolysis Bullosa
Primary: Number of Subjects Reported at Least One Adverse Event, Safety Population — 9 Participants
Obstructive Sleep Apnea
Primary: Change in Hypoxic Burden (HB) Log10HB[(%*Min)/Hour] — -0.41; -0.36; -0.04; -0.06 Log10HB4%[%min/hour]
Crohn's Disease
Primary: Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) — 6; 6; 7; 3 Participants