17,261 trials
Squamous Cell Lung Carcinoma
Primary: Objective Response Rate (ORR) — 0 Participants
Knee Osteoarthritis
Primary: Primary Endpoint: WOMAC Pain Score (Likert Scale Version) at 4 Weeks — 8.08; 6.73 units on a scale
AL Amyloidosis
Primary: Assessing Dose-limiting Toxicity to Determine Maximal Tolerated Dosage at 2 Milligram Dose — 0 Participants
Recurrent Plasma Cell Myeloma · Refractory Plasma Cell Myeloma
Primary: Number of Phase I Participants With Dose-Limiting Toxicity Events (Phase I) — 0; 0; 0; 0 Participants
Lymphoma
Primary: Event-free Survival (EFS) of Patients — 51 Participants
Acute Myeloid Leukemia · Myelodysplastic Syndrome
Primary: Number of Participants With Donor Neutrophil Engraftment — 3; 7; 1 Participants
Emphysema
Primary: Will Ibuprofen, 600 mg Three Times Daily, Decrease PGE Concentration in the Alveolar Portion of BAL Fluid in Subjects With Emphysema in Comparison to Placebo? — 0.003…
B-Cell Chronic Lymphocytic Leukemia
Primary: Overall Response Rate — 7 Participants
Adult B Acute Lymphoblastic Leukemia · Adult Nasal Type Extranodal NK/T-Cell Lymphoma · Adult Solid Neoplasm
Primary: Maximum Tolerated Dose of Veliparib When Combined With Bendamustine Hydrochloride — 300 mg
X-Linked Hypophosphatemia
Primary: Number of Participants With Adverse Events (AEs), Treatment Emergent AEs (TEAEs), Serious AEs (SAEs), and AEs Leading to Discontinuation or Death — 20; 20; 12; 9…
Metastatic Ureter Carcinoma · Metastatic Urethral Carcinoma · Stage III Bladder Urothelial Carcinoma AJCC v6 and v7
Primary: Observed Overall Response Rate — 50 percentage of participants
Graft Versus Host Disease · Leukemia · Lymphoma
Primary: Overall Response Rate — 12; 1; 7 Participants
Colorectal Cancer
Primary: Progression Free Survival — 7.33; 9.13 Months — p=0.046
Myasthenia Gravis
Primary: Proportion of Patients Whose Quantitative Myasthenia Gravis Scores Are Increased by no More Than 3 Points at the End of the SCIg Treatment Phase — 0.864 proportion of…
Asthma
Primary: Peak FEV1 (L) Defined as the Highest Bronchodilatory Effect on FEV1 During a Period of 5 Min to 4 h After the Last Evening Dose of Each Treatment Period — 2.792; 2.779…