Asitri Dashboard Search Clinical Trials
The U.S. National Library of Medicine provides a database of clinical trials worldwide. Use the fields below to search the database. Expand your results and select terms or phrases and right-click to search using Google, MalaCards, MedlinePlus, PubMed, or Wikipedia.
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Clinical Trials Search Results
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Count: 3279
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| NCT ID | Title | ||
|---|---|---|---|
| NCT01961908 | Open-Label Extension Study to ZPE-202 | ||
| NCT06363461 | Study of TDM-180935 in Atopic Dermatitis Patients | ||
| NCT01607294 | A Single Center Study to Evaluate the Efficacy and Safety of ETC 1002 in Subjects With Type 2 Diabetes | ||
| NCT06745973 | An Exploratory Clinical Study Evaluating EPI-003 Injection for the Treatment of Chronic Hepatitis B | ||
| NCT04645797 | A Dose Escalation Study of APR003 in Patients With Advanced Colorectal Cancer (CRC) With Malignant Liver Lesions | ||
| NCT04737486 | A First-in-Human Study of AV-001 in Healthy Subjects | ||
| NCT03742518 | A Study Evaluating the Efficacy and Safety of SM04554 Topical Solution in Male Subjects With Androgenetic Alopecia | ||
| NCT01555242 | A Study of Aneustat (OMN54) in Patients With Advanced Cancer and Lymphomas | ||
| NCT04045769 | A Study to Evaluate the Effect of Saroglitazar Magnesium on the QTc Interval in Healthy Volunteers | ||
| NCT06089668 | An Observational Study to Evaluate Clinical Characteristics of Adult Patients With Suspected or Confirmed Melioidosis | ||
| NCT04914286 | A Study of GFH018 in Combination With Toripalimab in Patients With Advanced Solid Tumors | ||
| NCT05876780 | A Gene Transfer Single Dose Study to Evaluate the Safety, Tolerability and Efficacy of SRP-9003 in Non-Ambulatory and Ambulatory Participants With Limb Girdle Muscular Dystrophy, Type 2E/R4 (Beta-Sarcoglycan [β-SG] Deficiency) | ||
| NCT03089762 | Intra-articular Injection in the Knee of Adipose Derived Stromal Cells and Platelet Rich Plasma for Osteoarthritis | ||
| NCT01798303 | A Study of LY2940094 in Participants With Alcohol Dependency | ||
| NCT05732103 | A Study of CTX-712 in Relapsed/Refractory Acute Myeloid Leukemia and Higher Risk Myelodysplastic Syndromes | ||
| NCT00243308 | Serp-1 for the Treatment of Acute Coronary Syndrome | ||
| NCT06825559 | Evaluate PK & Safety of Saroglitazar in Subjects With Moderate Hepatic Impairment Due to Cholestatic Liver Disease | ||
| NCT00911586 | Pharmacokinetic Study to Determine Time to Steady-state | ||
| NCT03927040 | Transcranial Electromagnetic Treatment Against Alzheimer's Disease | ||
| NCT00511576 | Study to Evaluate Combination Treatment of MGCD0103 and Docetaxel (Taxotere®) for Subjects With Advanced Cancer Tumors | ||
| NCT03832517 | Single and Multiple Dose Escalation Trial of an Intravenous Antibiotic RC-01 | ||
| NCT03997968 | A Phase 1/2 Study of CYT-0851 in B-Cell Malignancies and Advanced Solid Tumors | ||
| NCT06907043 | A Study of PARP1 Selective Inhibitor, EIK1004 (IMP1707) in Participants With Advanced Solid Tumors. | ||
| NCT02042950 | A Phase II Study of Carfilzomib in the Treatment of Relapsed/Refractory Mantle Cell Lymphoma | ||
| NCT04123574 | A Pilot Study of BXCL701 in Patients With Pancreatic Cancer | ||
| NCT05276310 | A Study of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy | ||
| NCT03371420 | PET Imaging of Subjects Using 124I-PU-AD | ||
| NCT05127590 | RBN-2397 in Combination With Pembrolizumab in Patients With SCCL | ||
| NCT02301897 | A Multi-Center, Parallel Design, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of 6 and 12 mg Proellex® (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Uterine Fibroids | ||
| NCT03122860 | A Study Evaluating the Safety and Efficacy of SM04690 for the Treatment of Moderately to Severely Symptomatic Knee Osteoarthritis | ||
| NCT02895100 | Safety and Efficacy Study of PTG-100 in the Treatment of Moderate to Severe Ulcerative Colitis | ||
| NCT04662632 | Abbreviated Protocol for Two-Stage Exchange | ||
| NCT03935555 | Assess the Safety, Tolerability Oral PU-H71 in Subjects Taking Ruxolitinib | ||
| NCT04476797 | Phase I/II Study of SBRT and GC4711 for Centrally Located or Large NSCLC | ||
| NCT06708897 | A Phase 1 Study of ZE50-0134 in Relapsed and Refractory Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, and Select Low-grad Lymphomas | ||
| NCT04355676 | Evaluation of Activity and Safety of Two Regimens of Low Dose Oral Selinexor in Participants With Moderate or Severe COVID-19 | ||
| NCT06780033 | A Study to Evaluate ART101 in Adult Participants With Hypertension | ||
| NCT01188408 | Efficacy and Safety Study of LE-DT to Treat Metastatic Castrate Resistant Prostate Cancer | ||
| NCT00219817 | Safety and Efficacy of RC-1291 HCl in Patients With Cancer Related Anorexia and Weight Loss | ||
| NCT05399368 | An Efficacy and Safety Study of RPT193 in Adults With Atopic Dermatitis | ||
| NCT00024674 | Study of SS1(dsFv)-PE38 (SS1P) Anti-Mesothelin Immunotoxin in Advanced Malignancies: Continuous Infusion for 10 Days | ||
| NCT04412018 | An Investigation on the Effects of Icosapent Ethyl (VascepaTM) on Inflammatory Biomarkers in Individuals With COVID-19 | ||
| NCT06597656 | A Gene Transfer Therapy to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) Following Therapeutic Plasma Exchange (Plasmapheresis) in Participants With Duchenne Muscular Dystrophy (DMD) and Pre-existing Antibodies to AAVrh74 | ||
| NCT05101902 | A Study to Determine Eligibility for CAH-301 (A Study of Gene Therapy for Classic Congenital Adrenal Hyperplasia (CAH) [NCT04783181]) | ||
| NCT04325464 | A Remote, 9-week Insomnia Treatment Trial to Collect Real World Data for a Digital Therapeutic | ||
| NCT05010629 | 9-ING-41 Plus Carboplatin in Salivary Gland Carcinoma | ||
| NCT02236195 | Study of Mocetinostat in Patients With Urothelial Carcinoma Having Inactivating Alterations of Specific Genes | ||
| NCT00320502 | A Phase 2 Study to Determine the Effects of BXT-51072 in Diabetic Patients Undergoing Angioplasty (PCI) | ||
| NCT05954312 | A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors | ||
| NCT01085045 | Study to Evaluate the Efficacy, Safety and Pharmacokinetics of PT001, PT003, and PT005 Following Chronic Dosing (7 Days) in Patients With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) |
