Clinical Trial Details
Trial ID: | L0803 |
Source ID: | JPRN-UMIN000030498 |
Associated Drug: | Dapagliflozin |
Title: | |
Acronym: | -- |
Status: | Recruiting |
Study Results: | No Results Available |
Results: | -- |
Conditions: | Type 2 diabetes mellitus |
Interventions: | Orally administration of 5mg Dapagliflozin once a day for 24weeks. |
Outcome Measures: | Evaluation of the change of hepatic lipid content measured by MRS at 24 weeks after starting<br> trial.Evaluation of the change of blood and urine examination at 4,12, and 24 weeks after starting<br> trial. <br>Evaluation of the change of microbiota at 24 weeks after starting trial. <br>Evaluation of the change of body composition<br> measured by InBody at 12 and 24 weeks after starting trial. <br>Evaluation of the change of CAP and LSM measured by Fibroscan at 12 and 24 weeks after starting trial. |
Sponsor/Collaborators: | Tokai University |
Gender: | All |
Age: | 20years-old80years-old |
Phases: | Not selected |
Enrollment: | 30 |
Study Type: | Interventional |
Study Designs: | Single arm Non-randomized |
Start Date: | 20/12/2017 |
Completion Date: | -- |
Results First Posted: | -- |
Last Update Posted: | 2 April 2019 |
Locations: | Japan |
URL: | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034810 |

Drug ID | Drug Name | Type | DrugBank ID | Targets | Category | Latest Progress | |
---|---|---|---|---|---|---|---|
D101 | Dapagliflozin | Chemical drug | DB06292 | SLC5A2 antagonist; SLC5A2 inhibitor | Antidiabetic drug | Under clinical trials | Details |
D094 | Cysteamine | Chemical drug | DB00847 | GSS stimulant | Renal drug | Under clinical trials | Details |
D095 | Cysteamine bitartrate | Chemical drug | DB00847 | -- | -- | Under clinical trials | Details |