65,437 trials
Fabry Disease
Primary: Number Of Participants Who Experienced Severe Treatment-emergent Adverse Events (TEAEs) — 0; 0; 0 Participants
Fabry Disease
Primary: Number Of Participants Who Experienced Severe Treatment-emergent Adverse Events (TEAEs) — 2 Participants
AMD (With Persistent or Recurrent Fluid Despite Monthly Intravitreal Anti-VEGF Therapy)
Primary: Proportion of Patients With no Fluid on OCT at Week 24
Melanoma
Primary: One-year Overall Survival Rate (OSR) Estimated by Complete Case Method — 83.08; 83.33; 100 Percentage of Participants
Leiomyomata
Primary: Number of Participants With Serious Adverse Events — 0; 0 Participants
End Stage Renal Disease
Primary: Number of Patients That Underwent Transplantation — 32 Participants
Endometriosis
Primary: Percentage of Responders at Month 3 Based on Daily Assessment of Dysmenorrhea (DYS) — 22.7; 43.4; 72.4 percentage of participants — p=< 0.001
Endometriosis, Pain
Primary: Change From Baseline in the Monthly Mean Numerical Rating Score (NRS) for Endometriosis Pain at Week 12 — -0.88; -1.19; -1.25 units on a scale — p=0.2311
Drug-Related Side Effects and Adverse Reactions
Primary: Mean Standardized Uptake Values (SUVs) Derived From Positron Emission Tomography-Computer Tomography (PET-CT) Data — 0.515; 0.566; 0.607; 0.623 Ratio
Fabry Disease
Primary: Number Of Participants Who Experienced Severe Treatment-emergent Adverse Events (TEAEs) — 0 Participants
Endometriosis
Primary: Percentage of Participants With a Response for Dysmenorrhea at Month 6 Based on Daily Assessment — 37.0; 57.1; 50.8; 75.9 percentage of participants
Carcinoma, Non-Small-Cell Lung
Primary: Incidence of Adverse Drug Reactions (ADRs) — 95.19 Percentage of Participants
Low Back Pain
Primary: Timed Get-Up-And Go — -1.84; -2.15; 1.11 seconds — p=0.08
Diabetes Mellitus, Type 2
Primary: Change in Glycated Haemoglobin A1c (HbA1c) (%) From Baseline After 24 Weeks of Treatment — -0.94; -0.12; -0.91; -0.33 Percentage (%) — p=<0.0001
Hereditary Angioedema (HAE)
Primary: Number of Participants With Treatment-emergent Adverse Events (TEAEs ) Including Serious Adverse Events (SAEs) — 8; 4; 3; 8 Participants