Bioequivalence Study Coadministered to Healthy Subjects in the Fasted State

Type 2 Diabetes Mellitus Clinical Trial

Official title:

A Bioequivalence Study of Fixed-dose Combination Tablet of 5 Milligrams Saxagliptin/10 Milligrams Dapagliflozin Relative to Their Respective Individual Components Coadministered to Healthy Subjects in the Fasted State

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02223065
• Other study ID #: CV181-364
• Status: Completed
• Phase: Phase 1
• First received: August 19, 2014
• Last updated: February 10, 2016
• Start date: September 2014
• Est. completion date: December 2014

Study information

• Verified date: February 2016
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate bioequivalence of coadministered drugs on healthy subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 19 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Signed Informed Consent Form

• Signed written informed consent must be obtained from the subjects in accordance with requirements of the study center's IRB or IEC before the initiation of any protocol-required procedures.

2. Target Population

• Healthy subjects as determined by no clinically significant deviation from normal in medical history, psychiatric history, physical examination findings, vital sign measurements, 12-lead ECG measurements, physical measurements, and clinical laboratory test results.

3. Age and Reproductive Status

• Males and females, ages 19 to 55 years, inclusive. To extent possible, the distribution of men and women between the sequences will be balanced

• Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the start of study drug.

• Women must not be breastfeeding. d) WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drugs saxagliptin and dapagliflozin plus 5 half lives of study drug dapagliflozin (the longer half life between the 2 drugs; 3 days) for a total of 3 days following treatment completion.

e) Men who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drugs saxagliptin and dapagliflozin plus 5 half lives of dapagliflozin (the longer half life between the 2 drugs; 3 days) for a total of 3 days following treatment completion.

f) Azoospermic males and WOCBP who are continuously not heterosexually active are exempt from contraceptive requirements. However, they must still undergo pregnancy testing as described in this section

Exclusion Criteria:

• Any significant acute or chronic medical illness.

• Current or recent (within 3 months of study drug administration) gastrointestinal disease that could impact upon the absorption of study drug

• Any other sound medical, psychiatric, and/or social reason as determined by the investigator

• Any major surgery within 4 weeks of study drug administration.

• Any prior GI surgery including cholecystectomy (remote history of appendectomy will not be exclusionary).

• Current, recent (within 3 months of study drug administration), or remote history of pancreatitis.

• Donation of blood or plasma to a blood bank or in a clinical study (except at screening visit) within 4 weeks before study drug administration.

• Blood transfusion within 4 weeks of study drug administration. h) Inability to tolerate oral medication.

• Inability to be venipunctured performed and/or tolerate venous access.

• Use of tobacco- or nicotine-containing products (including, but not limited to, cigarettes, pipes, e-cigarettes, cigars, chewing tobacco, nicotine patches, nicotine lozenges, or nicotine gum) within 6 months before check-in.

• Drug or alcohol abuse (within 2 years of study drug administration) as defined in the Diagnostic and Statistical Manual of Mental Disorders - 4th Edition, Diagnostic Criteria for Drug and Alcohol Abuse History of glucose intolerance or diabetes mellitus.

• For females, history of chronic or recurrent urinary tract infection (UTI) (defined as 3 occurrences per year) or UTI in the past 3 months. For males, any UTI within the previous 5 years that has not been thoroughly evaluated and for which an explanation is not clear.

• History of recurrent (defined as 3 occurrences per year) or recent vulvovaginal mycotic infections.

• Any other sound medical, psychiatric, and/or social reason as determined by the investigator.

Physical and Laboratory Test Findings

1. Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECGs, or clinical laboratory determinations beyond what is consistent with the target population.

2. Abnormal urinalysis at screening (may repeat once). If the urinalysis is abnormal on Day -1 of Period 1, continuation in the study is up to the investigator's discretion. The CRO medical monitor should be consulted.

3. Glucosuria or hematoria at screening or Day -1 of Period 1, repeat is not permitted. d) A positive nicotine test (ie, cotinine).

e) Abnormal liver function tests (alanine or aspartate aminotransferase [ALT or AST, respectively], or total bilirubin).

f) Any of the following on 12-lead ECG prior to study drug administration, confirmed by repeat.

i) PR = 210 ms ii) QRS = 120 ms iii) QT = 500 ms iv) QTcF = 450 ms g) Positive urine screen for drugs of abuse. h) Positive urine alcohol test. i) Positive blood screen for hepatitis C virus (HCV) antibody, hepatitis B surface antigen (HBsAg), or human immunodeficiency virus (HIV)-1 or HIV-2 antibodies at screening.

4. Allergies and Adverse Drug Reaction

1. History of allergy or adverse reactions to DPP4 or SGLT inhibitors or related compounds.

2. History of any significant drug allergy (such as anaphylaxis or hepatotoxicity).

5. Other Exclusion Criteria

1. Prisoners or subjects who are involuntarily incarcerated.

2. Subjects who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness.

3. Inability to comply with restrictions and prohibited activities/treatments

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 2
• Type 2 Diabetes Mellitus

Intervention

Drug:
• Saxagliptin

• Dapagliflozin

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum observed plasma concentration (Cmax) for saxagliptin and dapagliflozin as derived from serial blood samples for the plasma pharmacokinetic analysis of saxagliptin and dapagliflozin		60 hour interval after dosing each period	No
Primary	(AUC(0-T)) for saxagliptin and dapagliflozin as derived from serial blood samples for the plasma pharmacokinetic analysis of saxagliptin and dapagliflozin.	Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC(0-T)) for saxagliptin and dapagliflozin as derived from serial blood samples for the plasma pharmacokinetic analysis of saxagliptin and dapagliflozin.	60 hour interval after dosing each period	No
Primary	(AUC(INF)) for saxagliptin and dapagliflozin as derived from serial blood samples for the plasma pharmacokinetic analysis of saxagliptin and dapagliflozin	Area under the concentration-time curve from time zero extrapolated to infinite time (AUC(INF)) for saxagliptin and dapagliflozin as derived from serial blood samples for the plasma pharmacokinetic analysis of saxagliptin and dapagliflozin	60 hour interval after dosing each period	No
Secondary	Safety assessments based on review of adverse events, vital sign measurements, electrocardiograms, physical examinations, and clinical laboratory tests.		Two to three months	Yes