Study of MEDI0382 in Combination With Dapagliflozin and Metformin in Overweight/Obese Participants With Type 2 Diabetes

MedImmune LLC49 enrolled

Overview

A Phase 2 study Comparing the effects on glucose control of MEDI0382 in combination with Dapagliflozin and Metformin compared to placebo in combination with Dapagliflozin and Metformin in overweight/obese participants with Type 2 Diabetes Mellitus (T2DM).

This is an exploratory randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of MEDI0382 versus placebo in overweight/obese participants with T2DM treated with metformin and dapagliflozin dual therapy. The study will enroll participants with T2DM treated either with metformin monotherapy or with metformin and dapagliflozin dual therapy. After the screening period, participants treated with metformin monotherapy only will enter a 4-week run-in period where participants will be administered oral dapagliflozin 10 mg a day, which will be provided by the sponsor. Enrolled participants that are already treated with metformin and dapagliflozin dual therapy will continue this dual therapy throughout the study and can be randomized after the screening period without entering the run-in period. All participants (ie, on monotherapy and dual therapy) entering the double-blind treatment period will receive dapagliflozin 10 mg a day, which will be provided by the sponsor. Participants in this study will participate for up to 20 weeks including a screening period of up to 60 days, a 4-week run-in period (for participants on metformin monotherapy only), a 4-week treatment period, and a 4-week follow-up post-treatment period.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Type 2 Diabetes Mellitus

Interventions

MEDI0382DRUG

Subcutaneous dose of MEDI0382 (titrated up from 100 μg for 7 days to 200 μg for 7 days and to 300 μg for 14 days).

PlaceboDRUG

Subcutaneous dose of placebo matched to MEDI0382.

DapaglifozinDRUG

Oral dose of dapaglifozin 10 mg tablet.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 115 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Male and female participants aged \>= 18 years at screening. 2. Provision of signed and dated informed consent form (ICF) prior to any study specific procedures. 3. Body mass index between 25 kg/m\^2 and 40 kg/m\^2 (inclusive) at screening. 4. Hemoglobin A1c range between 7.0% and 10.0% (inclusive) at the time of screening. 5. Diagnosed with T2DM and treated with of metformin monotherapy (MTD \> 1 g) at least 8 weeks prior to screening or treated with stable, oral doses of dapagliflozin 10 mg and metformin (MTD \> 1 g) for at least 3 months prior screening. 6. Participants prescribed oral dual therapy with sulphonylurea, glitinide, or dipeptidyl peptidase-4 inhibitor (in addition to metformin) may be eligible to enter the study following a washout period of these medications totaling at least 28 days before initial screening evaluations have been completed. 7. Participants treated with stable doses of metformin (MTD \> 1 g) with canagliflozin (maximum dose of 300 mg/day), or metformin (MTD \> 1 g) with empaglifozin (maximum dose of 25mg/day) for at least 3 months prior to screening may be eligible to enter the study after switching to dapagliflozin. 8. Female participants of childbearing potential must have a negative pregnancy test at screening and randomization and must not be lactating. 9. Females of childbearing potential who are sexually active with a nonsterilized male partner must use at least one highly effective method of contraception from screening and must agree to continue using such precautions through to the end of the study. It is strongly recommended for the male partner of a female participant to also use male condom plus spermicide throughout this period. Cessation of contraception after this point should be discussed with a responsible physician. Periodic abstinence, the rhythm method, and the withdrawal method are not acceptable methods of contraception. Exclusion Criteria: 1. History of, or any existing condition that in the opinion of the investigator would interfere with evaluation of the investigational product, put the participant at risk, influence the participant's ability to participate, or affect the interpretation of the results of the study and/or any participant unable or unwilling to follow study procedures. 2. Any participant who has received another investigational product not included in the protocol as part of a clinical trial or a glucagon-like peptide-1 (GLP-1) analogue or sodium-glucose cotransporter-2 (SGLT2)-containing preparation (excluding dapagliflozin, canagliflozin, empagliflozin) within the last 30 days or 5 half-lives of the drug (whichever is longest) at the time of screening. 3. Any participant who has received any of the following medications prior to the start of the screening period (Visit 1) or prior to the study start period (Visit 4): * Concurrent use of any medicinal products, or herbal or over-the-counter (OTC) preparations licensed for control of body weight or appetite at the time of screening (Visit 1) * Concurrent or previous use of drugs approved for weight loss (eg, orlistat, bupropion-naltrexone, phentermine-topiramate, phentermine, lorcaserin) within the last 30 days or 5 half-lives of the drug (whichever is longest) at the time of screening (Visit 1) * Concurrent use of aspirin (acetylsalicylic acid) at a dose greater than 150 mg once daily and within the last 72 hours prior to the start of the study (Visit 4) * Concurrent use of paracetamol (acetaminophen) or paracetamol-containing preparations at a total daily dose of greater than 3000 mg and within the last 72 hours prior to the start of the study (Visit 4) * Concurrent use of ascorbic acid (vitamin C) supplements at a total daily dose greater than 1000 mg and within the last 72 hours prior to the start of the study (Visit 4) * Concurrent use of opiates, domperidone, metoclopramide, or other drugs known to alter gastric emptying and within the last 72 hours prior to the start of the study (Visit 4) 4. Concurrent participation in another study of any kind and repeat randomization in this study is prohibited. 5. Severe allergy/hypersensitivity to any of the proposed study treatments or excipients. 6. Diagnosis of type 1 diabetes mellitus, maturity-onset diabetes of the young, or latent autoimmune diabetes of adulthood or presence of anti-glutamic acid decarboxylase, anti-islet cell, or anti-insulin antibodies. 7. Symptoms of acutely decompensate blood glucose control (eg, thirst, polyuria, weight loss) at screening or randomization, a history of diabetes ketoacidosis (DKA), or hyperosmolar nonketotic coma or treatment with daily subcutaneous insulin within 90 days prior to screening. 8. Fasting hyperglycemia (\> 250 mg/dL/ \> 13.9 mmol/L) prior to randomization. 9. C-peptide level \< lower limit of normal (LLN). 10. History of acute or chronic pancreatitis or pancreatectomy. 11. Hypertriglyceridemia (\> 400 mg/dL) at screening. 12. Significant inflammatory bowel disease, gastroparesis, or other severe disease or surgery affecting the upper gastrointestinal (GI) tract (including weight-reducing surgery and procedures) which may affect gastric emptying or could affect the interpretation of safety and tolerability data. 13. Significant hepatic disease (except for nonalcoholic steatohepatitis or nonalcoholic fatty liver disease without portal hypertension or cirrhosis) and/or participants with any of the following results at screening: * Aspartate transaminase (AST) \>= 3 × upper limit of normal (ULN) * Alanine transaminase (ALT) \>= 3 × ULN * Total bilirubin (TBL) \>= 2 × ULN 14. Impaired renal function defined as estimated glomerular filtration rate (eGFR) \<= 60 mL/minute/1.73m\^2 at screening (eGFR according to Modification of Diet in Renal Disease \[MDRD\] using the isotope dilution mass spectrometry-traceable MDRD Study Equation (SI units). 15. Use of loop diuretics within 1 month prior to screening. 16. Poorly controlled hypertension as defined below: * Systolic blood pressure (BP) \> 160 mm Hg * Diastolic BP or \>= 100 mm Hg After 10 minutes of supine rest and confirmed by repeated measurement at screening (Visit 1 for all participants). 17. Unstable angina pectoris, myocardial infarction, transient ischemic attack, or stroke within 3 months prior to screening, or participants who have undergone percutaneous coronary intervention or a coronary artery bypass graft within the past 6 months or who are due to undergo these procedures at the time of screening. 18. Severe congestive heart failure (New York Heart Association Class III and IV) 19. Basal calcitonin level \> 50 ng/L at screening or history/family history of medullary thyroid carcinoma or multiple endocrine neoplasia. 20. Hemoglobinopathy, hemolytic anemia, or chronic anemia (hemoglobin concentration \< 11.5 g/dL \[115 g/L\] for males and \< 10.5 g/dL \[105 g/L\] for females) at screening or any other condition known to interfere with interpretation of HbA1c measurement. 21. History of neoplastic disease within 5 years prior to screening, except for adequately treated basal cell skin cancer, squamous cell skin cancer, or in situ cervical cancer. 22. Any positive results for serum hepatitis B surface antigen, hepatitis C antibody, and human immunodeficiency virus antibody. 23. Recent viral infection or illness requiring the use of antibiotics in the month prior to screening (Visit 1) for participants on dual therapy or prior to run-in period (Visit 2) for participants on monotherapy. 24. History of recurrent (at least 2) urinary tract and/or genital tract infections (including mycotic infections such as thrush) within 6 months prior to screening. 25. Substance dependence likely to impact participant safety or compliance with study procedures. 26. Involvement of any AstraZeneca, MedImmune, contract research organization, or study site employees and their close relatives.

Locations (8)

Research Site

Magdeburg, Germany

Research Site

Mannheim, Germany

Research Site

München, Germany

Research Site

Balatonfüred, Hungary

Outcomes

Primary Outcomes

Change From Baseline to Day 28 in Plasma Glucose Area Under the Concentration Time-curve From Time 0 to 4 Hours (AUC0-4hrs) as Measured by Mixed-meal Tolerance Test (MMTT)

The MMTT test involved the consumption of a standardised liquid meal (nutritional supplement of fat, carbohydrate, and protein) within 5 minutes. On Day -1 and on Day 28, following a minimum 10 hour fast, serial of blood samples were obtained prior and through 240 minutes after consumption of standardized meal for the measurement of glucose metabolism (with no additional food intake during this time).

Time frame: Zero minutes before and 15, 30, 45, 60, 90, 120, 180, and 240 minutes after consumption of the standardised meal on Day -1 (Baseline) and Day 28

Percent Change From Baseline to Day 28 in Plasma Glucose AUC0-4hrs as Measured by MMTT

The MMTT test involved the consumption of a standardised liquid meal (nutritional supplement of fat, carbohydrate, and protein)within 5 minutes. On Day -1 and on Day 28, following a minimum 10-hour fast, serial of blood samples were obtained prior and through 240 minutes after consumption of standardized meal for the measurement of glucose metabolism (with no additional food intake during this time).

Time frame: Zero minutes before and 15, 30, 45, 60, 90, 120, 180, and 240 minutes after consumption of the standardised meal on Day -1 (Baseline) and Day 28

Secondary Outcomes

Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Treatment-emergent Serious Adverse Events (TESAEs)

An adverse event (AE) is any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. A serious adverse event (SAE) is an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life threatening experience(immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. The TEAEs are defined as events present at baseline that worsened in intensity after administration of study drug or events absent at baseline that emerged after administration of study drug.

Data from ClinicalTrials.gov

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Oral dose of metformin tablet (maximum tolerated dose \[MTD\] \> 1 g).

Research Site

Miskolc, Hungary

Research Site

Szeged, Hungary

Research Site

Manchester, United Kingdom

Research Site

Rotherham, United Kingdom

Time frame: Day 1 through 28 days after the last dose of MEDI0382 (approximately 8 weeks)

Number of Participants With Abnormal 12-lead Electrocardiogram (ECG) Reported as TEAEs

Number of participants with abnormal 12-lead ECG reported as TEAEs are reported.

Time frame: Day 1 through 28 days after the last dose of MEDI0382 (approximately 8 weeks)

Number of Participants With Abnormal Vital Signs Reported as TEAEs

Number of participants with abnormal vital signs reported as TEAEs are reported.

Time frame: Day 1 through 28 days after the last dose of MEDI0382 (approximately 8 weeks)

Number of Participants With Abnormal Physical Examinations Reported as TEAEs

Number of participants with abnormal physical examinations reported as TEAEs are reported.

Time frame: Day 1 through 28 days after the last dose of MEDI0382 (approximately 8 weeks)

Number of Participants With Abnormal Clinical Laboratory Parameters Reported as TEAEs

Number of participants with abnormal clinical laboratory parameters reported as TEAEs are reported.

Time frame: Day 1 through 28 days after the last dose of MEDI0382 (approximately 8 weeks)

Area Under the Plasma Concentration Time Curve From Time Zero to Infinity (AUC [0-∞]) of MEDI0382

Area under the plasma concentration time curve from time zero to infinity (AUC \[0-∞\]) of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Area Under the Plasma Concentration Time Curve From Time Zero to Infinity (AUC [0-∞]) of Dapagliflozin

Area under the plasma concentration time curve from time zero to infinity (AUC \[0-∞\]) of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Area Under the Plasma Concentration-time Curve During the Dosing Period (AUCtau) of MEDI0382

Area under the plasma concentration-time curve during the dosing period (AUCtau) of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Area Under the Plasma Concentration-time Curve During the Dosing Period (AUCtau) of Dapagliflozin

Area under the plasma Concentration-time curve during the dosing period (AUCtau) of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Maximum Observed Serum Concentration (Cmax) of MEDI0382

Maximum observed serum concentration (Cmax) of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Maximum Observed Serum Concentration (Cmax) of Dapagliflozin

Maximum observed serum concentration (Cmax) of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Time to Reach Maximum Observed Serum Concentration (Tmax) of MEDI0382

Time to reach maximum observed serum concentration (Tmax) of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Time to Reach Maximum Observed Serum Concentration (Tmax) of Dapagliflozin

Time to reach maximum observed serum concentration (Tmax) of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Terminal Elimination Half-life (t½) of MEDI0382

Terminal half-life is the time required for the plasma concentration to fall by 50% during the terminal phase. The t½ of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Terminal Elimination Half-life (t½) of Dapagliflozin

Terminal half-life is the time required for the plasma concentration to fall by 50% during the terminal phase. The t½ of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Apparent Clearance (CL/F) of MEDI0382

Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. The CL/F of MEDI0382 is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days 7, 14, and 28

Apparent Clearance (CL/F) of Dapagliflozin

Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. The CL/F of Dapagliflozin is reported.

Time frame: Pre-dose and 0.5, 1, 2, 4, 6, 8, 12, and 24 hrs post-dose on Days -1, 7, 14, and 28

Number of Participants With Positive Anti-drug Antibodies (ADA) Titer to MEDI0382

Number of participants with positive Anti-drug antibodies (ADA) titer to MEDI0382 are reported.

Time frame: Day 1 (pre-dose), on Day 29 , and 28 days post last dose (end of study visit; approximately 8 weeks)

Change From Baseline in Plasma Glucose AUC24-hrs to the End of Each Dosing Level as Measured by Continuous Glucose Monitoring (CGM)

Continuous glucose monitoring is a minimally invasive device applied to the skin in the upper arm that provides a measure of interstitial glucose levels every 15 minutes. Continuous glucose monitoring measures glucose excursions during different meals and at different times of the day. End of dosing: Day 7 for MEDI0382 100 μg; Day 14 for MEDI0382 200 μg; and Day 28 for MEDI0382 300 μg.