NCT00101946 Nine-Weeks Treatment With 683699 In Subjects With Moderately-To-Severely Active Crohn's Disease Status COMPLETED Phase PHASE2
NCT00097409 Ispinesib In Subjects With Platinum-Taxane-Refractory Or Resistant Relapsed Ovarian Cancer Status COMPLETED Phase PHASE2
NCT00097370 Open-Label Extension Of Intravenous Mepolizumab In Patients With Hypereosinophilic Syndrome Status TERMINATED Phase PHASE3
NCT00097331 Three Months Treatment With SB683699 In Patients With Relapsing Multiple Sclerosis Status COMPLETED Phase PHASE2
NCT00095654 The DREAM (Diabetes Reduction Assessment With Ramipril and Rosiglitazone Medication) Trial Status COMPLETED Phase PHASE3
NCT00094367 A Study Comparing Safety Of Abacavir And Lamivudine Administered Once-Daily As A Single Tablet Versus The Same Drugs Administered Twice-Daily As Separate Tablets (ALOHA Study) Status COMPLETED Phase PHASE3
NCT00092274 Study of HuMax-CD20, a New Drug to Treat Early Stage Non-Hodgkin´s Follicular Lymphoma Status WITHDRAWN Phase PHASE1/PHASE2
NCT00090103 Benign Prostatic Hyperplasia Trial With Dutasteride And Tamsulosin Combination Treatment Status COMPLETED Phase PHASE3
NCT00090077 Monotherapy Versus Placebo Over 7 Days-Non-Nucleoside Reverse Transcriptase Inhibitor-Experienced HIV1 Infected Adults Status COMPLETED Phase PHASE1
NCT00089999 Lapatinib In Chemotherapy-Naive Or Metastatic Breast Cancer Status COMPLETED Phase PHASE2
NCT00089986 GR270773 In The Treatment Of Suspected Or Confirmed Gram-Negative Severe Sepsis In Adults Status COMPLETED Phase PHASE2
NCT00089583 48-Week Study Of GW433908 And Ritonavir Or GW433908 Alone, Twice Daily In Pediatric Patients With HIV Infection Status COMPLETED Phase PHASE2
NCT00086658 Intravenous Mepolizumab In Subjects With Hypereosinophilic Syndromes (HES) Status COMPLETED Phase PHASE3
NCT00086593 Study Of An FDA-approved Drug As Additional Therapy In Patients With Schizophrenia Status COMPLETED Phase PHASE3
NCT00085943 KALETRA Or LEXIVA With Ritonavir Combined With EPIVIR And Abacavir In Naive Subjects Over 48 Weeks Status COMPLETED Phase PHASE3
NCT00085904 Dose-Escalating Study Of SB-485232 Administered Intravenously Every 28 Days To Adults With Solid Tumors Or Lymphomas Status COMPLETED Phase PHASE1