65,437 trials
Healthy Volunteers · hATTR Amyloidosis
Primary: Number of Participants With at Least One Treatment-Emergent Adverse Event (TEAE) — 3; 1; 3; 7 Participants
Advanced Cancer
Primary: Objective Response Rate (ORR) Per Investigator — 20; 30; 17.4; 3.1 Percent of participants
Melanoma
Primary: Objective Response Rate (ORR) Per Blinded Independent Central Review (BICR) — 27.7; 36.0 Percentage of participants — p=0.0311
Respiratory Syncytial Virus Infections
Primary: Percentage of Subjects With Any Solicited Local Adverse Event (AEs) [Primary Study] — 5.9; 5; 5.8; 5.9 Percentage of participants
HIV Infections
Primary: Efficacy as Determined by the Proportion of Women in Each Arm With HIV-1 Seroconversion After 120 Endpoints Are Observed in the Trial. — 71; 97 Participants
Systemic Lupus Erythematosus
Primary: Number of Participants Achieving a Combined Clinical Response Using the Systemic Lupus Erythematosus (SLE) Responder Index (SRI) at Week 24 — 37; 31 Participants…
Pregnancy
Primary: Total Visit Number — 7.9; 10.2 visits — p=<0.001
Human Immunodeficiency Virus
Primary: HIV Incidence Per 100 Person Years — 1.18; .98 cases per 100 person years
Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma
Primary: Objective Response Rate (ORR) Based on Independent Reviewer Assessment — 76.5; 100.0 percentage of participants
Contact Lens Complication · Dry Eye
Primary: Visual Analog Scale (VAS) Ocular Comfort — 36.66; 38.06; 33.68; 39.36 units on a scale — p=0.07
Dental Implant · Immediate Dental Implant · Soft Tissue Augmentation
Primary: Change in Ridge Dimension — -1.65; -1.87; -1.44; -1.37 millimeters (mm)
Caregiver Burden
Primary: Modified Zarit Burden Interview — 19.429; 17.950; 32.207; 27.160 Burden score — p=0.206
Pelvic Organ Prolapse · Urogenital Prolapse · Vaginal Vault Prolapse
Primary: Surgical "Failure" Defined by (i) Anatomic Assessment of Prolapse, (ii) Presence of Bulge Symptoms, and/or (Iii) Retreatment of Prolapse — 18; 8 Participants
Motor OFF Episodes Associated With Parkinson's Disease
Primary: Change From Pre-dose to 90 Mins. Post-dose in Movement Disorders Society Unified Parkinson's Disease Rating Scale Part III Score After 4 Weeks of Dosing in Each…
Psoriasis
Primary: Percentage of Participants With a Modified sPGA-G Response at Week 16 — 19.5; 39.6 Percentage of participants — p=0.0003