Jardiance® Post Marketing Surveillance (PMS) in Korean Patients With Chronic Heart Failure
Study Details
Study Description
Brief Summary
The primary objective of this study is to monitor the safety profile of Jardiance® in Korean patient with chronic heart failure (New York Heart Association (NYHA) class II-IV) in a routine clinical setting.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Patients who have started at first time on Jardiance®
|
Drug: JARDIANCE®
JARDIANCE® film-coated tablets 10mg
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Incidence rates of patients with adverse events [up to 24 weeks]
Adverse events will include: Adverse events, unexpected adverse events, unexpected adverse drug reaction, serious adverse events, serious adverse drug reaction, drug-related adverse events, non-serious adverse drug reaction, adverse event of special interest, adverse events leading to discontinuation.
Secondary Outcome Measures
- Occurrence of hospitalization for heart failure (first and recurrent) after 12 weeks of treatment from baseline [at week 12]
- Occurrence of hospitalization for heart failure (first and recurrent) after 24 weeks of treatment from baseline [at week 24]
- Occurrence of cardiovascular death after 12 weeks of treatment [at week 12]
- Occurrence of cardiovascular death after 24 weeks of treatment [at week 24]
- Changes from baseline in New York Heart Association (NYHA) functional class after 12 weeks of treatments [at baseline, at week 12]
- Changes from baseline in New York Heart Association (NYHA) functional class after 24 weeks of treatments [at baseline, at week 24]
- Changes in ejection fraction (EF) (if available) at 12 weeks compared to baseline [at baseline, at week 12]
- Changes in ejection fraction (EF) (if available) at 24 weeks compared to baseline [at baseline, at week 24]
- Changes in B-type Natriuretic Peptide (BNP) or N-terminal prohormone of brain natriuretic peptide (NT-proBNP) (if available) at 12 weeks compared to baseline [at baseline, at week 12]
- Changes in B-type Natriuretic Peptide (BNP) or N-terminal prohormone of brain natriuretic peptide (NT-proBNP) (if available) at 24 weeks compared to baseline [at baseline, at week 24]
- Changes in glycated hemoglobin (HbA1c) (if available in Type 2 Diabetes (T2D) patients) after 12 weeks of treatment [at baseline, at week 12]
- Changes in Fasting Plasma Glucose (FPG) (if available in Type 2 Diabetes (T2D) patients) after 12 weeks of treatment [at baseline, at week 12]
- Changes in glycated hemoglobin (HbA1c) (if available in Type 2 Diabetes (T2D) patients) after 24 weeks of treatment [at baseline, at week 24]
- Changes in Fasting Plasma Glucose (FPG) (if available in Type 2 Diabetes (T2D) patients) after 24 weeks of treatment [at baseline, at week 24]
- Change from baseline in estimated Glomerular Filtration Rate (eGFR) (if available) after 12 weeks of treatment [at baseline, at week 12]
- Change from baseline in estimated Glomerular Filtration Rate (eGFR) (if available) after 24 weeks of treatment [at baseline, at week 24]
- Change from baseline in body weight after 12 weeks of treatment [at baseline, at week 12]
- Change from baseline in body weight after 24 weeks of treatment [at baseline, at week 24]
- Change from baseline in blood pressure (systolic blood pressure (SBP), diastolic blood pressure (DBP)) after 12 weeks of treatment [at baseline, at week 12]
- Change from baseline in blood pressure (systolic blood pressure (SBP), diastolic blood pressure (DBP)) after 24 weeks of treatment [at baseline, at week 24]
Eligibility Criteria
Criteria
Inclusion criteria:
-
Patients who have started at first time on Jardiance® in accordance with the approved label in Korea for heart failure (HF)
-
Chronic heart failure (New York Heart Association (NYHA) class II-IV)
-
Age ≥ 19 years at enrolment
-
Patients who have signed on the data release consent form
Exclusion criteria:
-
Patients with previous exposure to Jardiance®
-
Known allergy or hypersensitivity to active ingredients empagliflozin or to any of the excipients
-
Patients with type 1 diabetes or with prior history of diabetic ketoacidosis (DKA)
-
Patient with renal impairment with estimated Glomerular Filtration Rate (eGFR) < 20 mL/min/1.73 m²
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Patients with rare hereditary conditions of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption
-
Patient who are pregnant or are nursing or who plan to become pregnant while in the trial
-
Patients for whom empagliflozin is contraindicated according local label of Jardiance®
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Boehringer Ingelheim Korea Ltd. | Seoul | Korea, Republic of |
Sponsors and Collaborators
- Boehringer Ingelheim
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 1245-0276