65,437 trials
Graft vs Host Disease
Primary: Participants That Developed Severity Score 3 or Higher Oral Chronic Graft Versus Host Disease (GVHD). — 7; 4 Participants
Pulmonary Arterial Hypertension
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs) up to 28 Days After Study Treatment Discontinuation — 527 Participants
Anxiety · Depression · Psychological Stress
Primary: Change From Baseline on an Aggregate Measure of Psychological Distress That Averages the Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety and…
Breast Cancer
Primary: Objective Response Rate (ORR) — 30; 30 percentage of participants
Acute Lymphoblastic Leukemia
Primary: Percentage of Participants With Continuous Complete Remission of Patients Receiving High-dose and Conventional Dose PEG-asparaginase. — 91.6; 90.7 Percentage of…
Lymphoma
Primary: Objective Response Rate (ORR) Based on Lugano Classification Criteria — 50.0; 33.3; 57.1; 58.3 percentage of participants
Episodic Cluster Headache · Chronic Cluster Headache
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious AEs (SAEs) — 119; 17 Participants
Barrett's Esophagus
Primary: Eradication of Barrett's Esophagus — 2 Participants
Acute Kidney Injury
Primary: Composite of Progression of AKI, Inpatient Dialysis, or Inpatient Death — 622; 653 Participants — p=0.67
Diabetes Mellitus, Type 2
Primary: Number of Participants With Ketoacidosis — 1; 1 Participants
Persistent Atrial Fibrillation
Primary: Primary Efficacy Endpoint - Number of Participants to Achieve Freedom From AF/AT/AFL. — 67; 25 Participants — p=0.0472
Lymphoma
Primary: Objective Response Rate (ORR) — 8.3; 39.0; 64.5; 71.4 percentage of participants
Lymphoma
Primary: Objective Response Rate With Parsaclisib Based on Lugano Classification Response Criteria — 65.2; 77.7 percentage of participants
Metastatic Renal Cell Cancer · Stage IV Renal Cell Cancer
Primary: Progression-free Survival (PFS) — 2.5 months
Hypercholesterolemia
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs) — 3; 5 Participants