Type 2 diabetes mellitus
Conditions
Sponsors
TAKEDA PHARMACEUTICAL COMPANY LTD.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. The participant has a diagnosis of type 2 diabetes mellitus. 2. The participant has a fasting C-peptide value of 0.6 ng/mL or higher at the start of the screening period (Week -6) and Week -2 of the screening period. 3. The participant has a hemoglobin value of 10.0 g/dL or higher at the start of the screening period (Week -6) and Week -2 of the screening period. 4. The participant has a Haemoglobin A1c (HbA1c) value of 7.0% or higher but less than 10.0% at Week -2 of the screening period. For participants undergoing hemodialysis (with End-stage Renal Disease [ESRD]), those with a glycoalbumin value of 20% or higher could be enrolled even if their HbA1c value is below 7.0% at Week -2 of the screening period. 5. [HbA1c value of 7.0% or higher but less than 10.0% at Week -2 of the screening period] The participant has an HbA1c value difference between the start of the screening period (Week -6) and Week -2 of the screening period within 10.0%* of the HbA1c value at the start of the screening period (Week -6). [For participants undergoing hemodialysis (with ESRD), glycoalbumin value of 20% or higher and HbA1c value of below 7.0% at Week -2 of the screening period] The participant has a glycoalbumin difference between the start of the screening period (Week -6) and Week -2 of the screening period within 10.0%* of the glycoalbumin value at the start of the screening period (Week -6). *: rounded to one decimal place 6. The participant has been on a fixed diet and/or exercise therapy (if any) for at least 6 weeks prior to the start of the screening period (Week -6). 7. The participant meets any of the following: - The participant has not received any antidiabetic medications (including insulin preparations) from at least 6 weeks prior to the start of the screening period (Week -6). - The participant is being treated with one oral hypoglycemic drug* starting from at least 6 weeks prior to the start of the screening period (Week -6) at a fixed dose and regimen. *: any one of the following medications: mitiglinide calcium hydrate, repaglinide, acarbose, miglitol, or voglibose - The participant is being treated with one insulin preparation** starting from at least 6 weeks prior to the start of the screening period (Week -6) at a fixed dose and regimen (=<40 units/day) of the insulin preparation. **: Any one of the following insulin monotherapies: mixed (short-acting or rapid-acting insulin containing no more than 30% volume), intermediate-acting, or long-acting soluble insulin preparations 8. The participant is not undergoing hemodialysis or peritoneal dialysis and has severe renal impairment [creatinine clearance (Ccr) <30 mL/min at the start of the screening period (Week -6)], or the participant is undergoing hemodialysis and has end-stage renal failure. 9. In the opinion of the investigator or sub-investigator, the initiation of hemodialysis or peritoneal dialysis at least within 12 weeks after starting the investigational product is not expected. [in cases where the participant is not undergoing hemodialysis or peritoneal dialysis (patients with severe renal impairment)] 10. The participant has been undergoing hemodialysis starting from at least 6 months prior to informed consent and, in the opinion of the investigator or sub-investigator, the participant is clinically stable. [in cases where the participant is undergoing hemodialysis (patient with end-stage renal failure)] 11. The participant is male or female and is aged 20 years or older
Exclusion criteria
Exclusion criteria: 1. The participant has clinically evident hepatic impairment [e.g., aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >=2.5 times the upper limit of normal or total bilirubin of >=2.0 mg/dL at the start of the screening period (Week -6) or at Week -2 of the screening period]. 2. The participant has any serious cardiac diseases, cerebrovascular disorders, or serious pancreatic or hematological diseases (e.g., participants who require inpatient treatment or are hospitalized for treatment within 24 weeks prior to the start of the screening period). 3. The participant has severe ketosis, diabetic coma or precoma, type 1 diabetes, severe infection, before or after surgery, or severe external trauma. 4. The participant has hemoglobinopathy (sickle cell disease, thalassemia, etc.). 5. The participant experienced hypoglycemia (participants with a blood glucose value of =<70 mg/dL or hypoglycemic symptoms) within 6 weeks prior to the start of the screening period or during the screening period (at least twice per week). 6. The participant has inadequately controlled hypertension. 7. For participants who are being treated with one antidiabetic agent, the participant was using at least two antidiabetic therapies on the day before 6 weeks prior to the start of the screening period (Week -6) (43 days prior to the start of the screening period). 8. The participant has malignancies. 9. The participant has a history of hypersensitivity or allergies to dipeptidyl peptidase 4 (DPP-4) inhibitors. 10. The participant has a history of gastrectomy or small intestinal resection. 11. The participant is a habitual drinker and consumes a daily average of more than 100 mL of alcohol. 12. The participant has a history of drug abuse (defined as the use of an illegal drug) or alcohol dependence. 13. The participant is required to take excluded medications during the study period. 14. The participant has previously received trelagliptin. 15. The participant received any other investigational products (including study drugs in a post-marketing clinical study) within 12 weeks prior to the start of the screening period. 16. The participant is participating in other clinical studies at the time of informed consent. 17. If female, the participant is pregnant or lactating or intending to become pregnant from the time of informed consent to within 1 month after the end of the study; or intending to donate ova during such time period. 18. The participant is an immediate family member of a study site employee, or is in a dependent relationship with a study site employee who is involved in the conduct of this study (e.g., spouse, parent, child, sibling) or may consent under duress. 19. The participant is hospitalized during the screening period or is deemed as requiring hospitalization during the study period by the investigator or subinvestigator, unless the hospitalization is for short-term evaluations including complete health checkups or shunt (including shunt maintenance). 20. The participant is deemed ineligible for the study for any other reason by the investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| efficacy Change from Baseline in HbA1c at the End of Treatment Period I Timeframe: Baseline (Week 0) and end of Treatment Period I (Up to Week 12) safety Number of Participants who had One or More Treatment Emergent Adverse Event (TEAE) Before the Start of Study Drug Administration in Treatment Period II Timeframe: Up to Week 12 An Adverse Event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a drug (including the study drug); it does not necessarily have to have a causal relationship with this treatment (including the study drug). An AE can therefore be any unfavorable and unintended sign (eg, a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug (including the study drug), whether or not it is considered related to the drug. A treatment-emergent adverse event (TEAE) is defined as an adverse event with an onset that occurs after receiving study drug. safety Number of Participants who had One or More TEAE Occurred After 1st Dose of Trelagliptin 25 mg Tablet Timeframe: Up to Week 54 An AE is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a drug (including the study drug). It does not necessarily have to have a causal relationship with this treatment (including the study drug). An AE can therefore be any unfavorable and unintended sign (eg, a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug (including the study drug), whether or not it is considered related to the drug. A TEAE is defined as an adverse event with an onset that occurs after receiving study drug. | — |
Secondary
| Measure | Time frame |
|---|---|
| efficacy Changes From Baseline in HbA1c Timeframe: Baseline (Week 0) and Week 2, 4, 8, 12, and End of Treatment Period I (up to Week 12) and Period II (up to Week 52) efficacy Number of Participants Achieving <6.0%, <7.0%, and <8.0% HbA1c at the End of Treatment Period I and Period II Timeframe: At the end of Treatment Period I (Up to Week 12) and Period II (Up to Week 52) efficacy Change From Baseline in Fasting Plasma Glucose at each time point Timeframe: Baseline (Week 0) and Week 2, 4, 8, 12, and end of Treatment Period I (up to Week 12) and Period II (up to Week 52) efficacy Change From Baseline in Glycoalbumin at each time point Timeframe: Baseline (Week 0) and Week 2, 4, 8, 12, and end of Treatment Period I (up to Week 12) and Period II (up to Week 52) safety Numbers of Participants with TEAE related to Vital Signs Before the Start of Study Drug Administration in Treatment Period II Timeframe: Up to Week 12 safety Number of Participants with Markedly Abnormal Values of 12-Lead Electrocardiogram (ECG) Parameters Before the Start of Study Drug Administration in Treatment Period II Timeframe: Up to Week 12 safety Number of Participants with Markedly Abnormal Values of Clinical Laboratory Parameters Before the Start of Study Drug Administration in Treatment Period II Timeframe: Up to Week 12 | — |
Countries
Japan
Outcome results
None listed