Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter, Therapeutic Exploratory Phase 2 Study to Evaluate the Efficacy and Safety of JP-2266 in Patients with Type 2 Diabetes Mellitus
Evaluation of efficacy and safety when administered JP-2266 in type 2 diabetes patients
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| JP-2266 Low-dose | Experimental | Subjects take the investigational products once a day for 12 weeks. |
|
| JP-2266 High-dose | Experimental | Subjects take the investigational products once a day for 12 weeks. |
|
| placebo | Experimental | Subjects take the investigational products once a day for 12 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SGLT2 inhibitor | Drug | SGLT 1/2 dual inhibitor |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in HbA1c at the 12 week from the baseline | 12 week |
Not provided
Not provided
Inclusion Criteria:
Adult aged 19 to 80 years
Those diagnosed with type 2 diabetes
A person who provides diet and exercise therapy for the management of diabetes from 8 weeks before the screening criteria and can continue diet and exercise therapy during the clinical trial
Screening Results of the following criteria
Patients with 20 < BMI ≤ 45 kg/㎡
Those who voluntarily signed the informed consent to participate in this study
Exclusion Criteria:
Any type of diabetes other than type 2 diabetes
Screening when the inspection meets the following criteria
A person with the following medical history or history of surgery/therapy
A person who has the following diseases or signs
A person who has a history of hypersensitivity to the ingredients of a clinical trial drug, SGLT1/SGLT2 inhibitor or SGLT-2 inhibitor
Pregnant or lactating women
Participants in interventional clinical trials subject to other IP or medical devices within 12 weeks prior to screening
If the investigator is deemed unsuitable for the subject of this clinical trial due to other reasons
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Severance Hospital | Seoul | Seodaemun-gu | 03722 | South Korea |
Not provided
| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D000077203 | Sodium-Glucose Transporter 2 Inhibitors |
| ID | Term |
|---|---|
| D045504 | Molecular Mechanisms of Pharmacological Action |
| D020228 | Pharmacologic Actions |
| D020164 | Chemical Actions and Uses |
| D007004 | Hypoglycemic Agents |
Not provided
Not provided
Not provided
Not provided
Not provided
Double blind
| D004700 | Endocrine System Diseases |
| D045505 | Physiological Effects of Drugs |