17,261 trials
Bladder Cancer
Primary: Arm A: Progression Free Survival (PFS) — 8 participants
Oral Malodor · Halitosis
Primary: Organoleptic Scores After the First Use of the Prescribed Method by 15 Minutes (Masking Effect), and After 7 Days of Use (Therapeutic Effect). — 2.10; 1.62; 1.36; 1.10…
Prostate Cancer
Primary: Percentage of Participants Experiencing Neither of the 2 Mineralocorticoid Excess Toxicity During the First 24 Weeks of Treatment — 70.6; 36.8; 60.0; 70.3 Percentage of…
Asthma
Primary: Mean Daily Dose at Study Termination Across Participants — 29.6 mg
Metastatic Breast Cancer
Primary: Number of Participants With Clinical Benefit (CBR) and Number of Participants With CBR Having a Disease Free Interval (DFI) Greater Than 2 Years - Evaluable Population…
Hemophilia B
Primary: Number of Subjects With Treatment-related Adverse Events — 0 participants
Cholesterol Ester Storage Disease (CESD) · Lysosomal Acid Lipase Deficiency · LAL-Deficiency
Primary: Number Of Participants Reporting TEAEs And IARs — 8; 1; 2; 0 Participants
Chronic Allergic Conjunctivitis
Primary: Ocular Itching — 1.80; 2.58; 1.72; 2.70 units on a scale (0 -4)
Kidney Transplantation
Primary: Response to Bortezomib Monotherapy — 0; 0; 0; 1 participants
Influenza
Primary: Percent MMID — 0; 0; 20; 47 percentage of participants
Smoking Cessation
Primary: Number of Participants Who Stopped Smoking by 12 Month Post Treatment — 31; 41 participants
Myelodysplastic Syndromes
Primary: Number of Participants Who Experienced an Adverse Event — 6 participants
Leukemia
Primary: Phase I: Maximum Tolerated Dose (MTD) of Sorafenib Given With Azacitidine — 400 mg/twice daily
Uterine Hemorrhage · Contraception
Primary: Cessation of Vaginal Bleeding — 37.5; 87.5 percentage of participants
Squamous Non Small Cell Lung Cancer
Primary: Percentage of Participants Who Achieve Best Overall Tumor Response of Complete Response (CR) or Partial Response (PR) (Objective Response Rates [ORR]) — 48.9; 40.0…