A Phase 1, Bioequivalence Study of SYR-472 25mg and 50mg Tablets

NCT ID: NCT02372097

Last Updated: 2023-12-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-03-31
• Study Completion Date: 2015-04-30

Brief Summary

The purpose of this study is to investigate the bioequivalence of 2 tablets of SYR-472 25 milligram (mg) and 1 tablet of SYR-472 50 mg administered to healthy adult males.

Detailed Description

Bioequivalence of 2 SYR-472 25 mg tablets and 1 SYR-472 50 mg tablet administered to healthy adult males will be investigated in a randomized, open-label, crossover study.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Group A

Participants in group A will be orally administered 2 tablets of SYR-472 25 mg in period 1 and 1 tablet of SYR-472 50 mg tablet in period 2, both in a single dose under fasting conditions in the morning.

Group Type: EXPERIMENTAL

SYR-472

Intervention Type: DRUG

SYR-472 25mg, 50mg

Group B

Participants in group B will be orally administered 1 tablet of SYR-472 50 mg in period 1 and 2 tablets of SYR-472 25 mg tablets in period 2, both in a single dose under fasting conditions in the morning.

Group Type: EXPERIMENTAL

SYR-472

Intervention Type: DRUG

SYR-472 25mg, 50mg

Interventions

SYR-472

SYR-472 25mg, 50mg

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Participants who understand the outline of the clinical study and are capable of complying with their responsibilities as participants, as judged by the investigator or sub investigator.

2. Participants who can sign and date the informed consent form before the initiation of the study procedure.

3. Healthy Japanese adult males.

4. Participants who are 20 to 35 years of age at the time of informed consent.

5. Participants who weigh 50.0 kilogram (kg) or more with a body mass index (BMI) of 18.5 to less than 25.0 kilogram per square meter (kg/m^2) in the screening period.

Exclusion Criteria

1. Participants who were administered any investigational product within 16 weeks (112 days) before the start of the study drug administration in stage 1.

2. Participants who have received SYR-472 in the past.

3. Employees of the study site, their family members, those who are in a dependency relationship with employees of the study site involved in the conduct of the study (for example [e.g.], spouse, parents, children, brothers and sisters), and those who might be coerced to consent to participate in the study.

4. Participants who have poorly controlled, clinically significant abnormalities of the nervous system, cardiovascular system, lung, liver, kidneys, metabolism, gastrointestinal system, urinary system, or endocrinological system, which possibly may affect study participation or study results.

5. Participants who have a positive urine drug test in the screening period.

6. Participants who need to use drugs or foods listed in the table of prohibited concomitant drugs and foods.

7. Participants who have a history of hypersensitivity or allergy to drugs (including SYR-472 and its ingredients).

8. Participants who currently have or recently had (within the past 6 months) gastrointestinal disease that may affect drug absorption (malabsorption, esophageal reflux, peptic ulcer disease, erosive esophagitis, frequent [at least once a week] heartburn, surgical intervention [e.g., cholecystectomy]).

9. Participants with a past history of cancer.

10. Participants who are positive for any of the following during the screening period: hepatitis B virus surface antigen (HBsAg), antibody against hepatitis C virus (HCV), human immunodeficiency virus (HIV) antigen, anti-HIV antibody, or serological test for syphilis.

11. Participants with difficulty having blood collected from a peripheral vein.

12. Participants who donated 200 milliliter (mL) or more of whole blood within the 4 weeks (28 days) or 400 mL or more of whole blood within the 12 weeks (84 days) before starting the study drug administration in stage 1.

13. Participants who donated a total of 800 mL or more of whole blood within the 52 weeks (364 days) before starting the study drug administration in stage 1.

14. Participants who donated blood components within the 2 weeks (14 days) before starting the study drug administration in stage 1.

15. Participants who show clinically significant abnormalities in electrocardiogram (ECG) during the screening period or on Day 1 (before the study drug administration).

16. Participants who have laboratory test abnormalities suggestive of a clinically significant primary disease or who have abnormal values in any of the following parameters: alanine aminotransferase (ALT) or aspartate serum transaminase AST exceeding 1.5 times the upper limit of the normal range.

17. Participants who are unlikely to comply with the study protocol or are ineligible for the study for any other reason, as judged by the investigator or sub investigator.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Takeda

Locations

Fukuoka, , Japan

Countries

Japan

Other Identifiers

U1111-1167-0746

Identifier Type: OTHER

Identifier Source: secondary_id

JapicCTI-152813

Identifier Type: REGISTRY

Identifier Source: secondary_id

JapicCTI-R160849

Identifier Type: REGISTRY

Identifier Source: secondary_id

SYR-472-1005

Identifier Type: -

Identifier Source: org_study_id