17,261 trials
Opioid-Related Disorders
Primary: SOWS: the Subjective Opiate Withdrawal Scale — 11.5; 12.5 units on a scale
Prevention of Meningococcal Disease
Primary: Percentages of Subjects With N.Meningitidis Human Serum Bactericidal Activity (hSBA) Titers≥ 1:4, After One Dose of Either MenACWY-CRM Vaccine, With Adjuvant or Without…
Primary Peritoneal Cavity Cancer · Recurrent Ovarian Epithelial Cancer
Primary: Tumor Response Duration — 3.9; 24.1 months
Breast Neoplasms
Primary: Percentage of Progression Free Participants After 16 Weeks of Treatment — 28.57; 0.00; 25.00 Percentage of participants
Functional Dyspepsia
Primary: Rate of Complete Dyspepsia Symptom Relief — 22.4; 29.3; 27.0; 17.9 Percentage of Participants
Cutaneous Leishmaniasis
Primary: Date of Clinical Cure — 2; 2; 15; 10 participants
Neuralgia, Postherpetic
Primary: Change From Baseline in the Average Pain Intensity Score at Week 12 — 6.13; 6.04; 6.05; -1.42 Score on a scale
Alzheimer Disease
Primary: Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) — 16; 22; 28; 1 participants
Acne Vulgaris
Primary: Proportion of Patients With Success According to the Dichotomized IGA Scale Based on Facial Assessments 12 Weeks After the First Treatment. Success is Defined as an…
Pancreatic Cancer
Primary: Overall Survival Rate at 6 Months — 58 percentage of participants
Melanoma
Primary: Response Rate (RR) — 1; 2; 1; 8 participants
Overweight · Obesity
Primary: Least Squares (LS) Mean Percent Change in Body Weight From Baseline to Week 28 - Evaluable Population — -2.01; -5.47; -5.83; -6.85 Percentage change in kg — p=<0.0001
Neoplasms
Primary: Objective Response (OR) — 1 Participants with OR
Chronic Obstructive Pulmonary Disease (COPD)
Primary: Forced Expiratory Volume in One Second (FEV1), Peak Effect Within 0 - 24 Hours Post-dose — 1.67; 1.73; 1.64 L
Carcinoma, Non-Small-Cell Lung
Primary: Phase I Step: Safety of BIBW 2992 Assessed Based on Incidence of Dose Limiting Toxicity (DLT) and Incidence & Intensity of Adverse Events According to CTCAE — 3; 3; 6; 3…