An Add-on Study of MLR-1023 in Adults With Uncontrolled Type 2 Diabetes on Metformin Therapy

A Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Add-on Study of MLR 1023 in Adults With Uncontrolled Type 2 Diabetes on Metformin Therapy

This Phase 2, multi-center, double-blind, randomized, placebo-controlled, parallel group, add-on study of MLR 1023 in adults with uncontrolled T2DM on metformin anti diabetic monotherapy is designed to evaluate the efficacy and safety of MLR 1023 in combination with metformin in subjects with uncontrolled T2DM.

Study Overview

• Status: Unknown
• Conditions: Type 2 Diabetes Mellitus
• Intervention / Treatment: Drug: MLR-1023; Other: Placebo

Detailed Description

Medical management of T2DM involves diet, exercise, weight management, and pharmacotherapy. Pharmacological agents, such as metformin, α-glucosidase inhibitors, orlistat, and thiazolidinediones, have been shown to decrease incident diabetes. Metformin has the strongest evidence base and demonstrated long-term safety as pharmacological therapy for diabetes treatment. The American Diabetes association position statement on diabetes care recommends that if Hemoglobin A1C (HbA1C) targets are not achieved after approximately 3 months of metformin anti-diabetic monotherapy, a combination of metformin and one of several oral treatment options should be considered.

In this study, subjects with a diagnosis of T2DM who are not adequately controlled (HbA1C between 7.0% and 10.0%, inclusive) and started metformin therapy at least 3 months prior to Screening will be recruited into the study. Subjects will continue taking metformin for the duration of the study and once daily oral MLR 1023 or placebo will be added to metformin.

The efficacious dose-level range of MLR 1023 in diabetic subjects is anticipated to be between 25 and 100 mg. Therefore, the efficacy, safety, and tolerability of 25 mg and 50 mg doses in addition to the 100 mg dose that was shown to be effective in the Phase 2a proof of concept study will be assessed.

• Study Type: Interventional
• Enrollment (Anticipated): 400
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • California
    • Los Angeles, California, United States, 90057
      • National Research Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Male or female, age 18 to 75 years, inclusive.
2. Diagnosis of T2DM.
3. Body mass index (BMI) between 20 and 40 kg/m2.
4. HbA1C between 7.0% and 10.0%.
5. Treated with metformin as the only anti-diabetic therapy.
6. Metformin dosage must have been stable and unchanged for at least 3 months prior to Screening and at a dose of at least 1,500 mg/day or the maximum tolerated dose if less than 1,500 mg/day.
7. Able and willing to comply with the study protocol for the duration of the study including scheduled clinic appointments.
8. Able and willing to provide written informed consent for study participation prior to performance of any study-related assessments.

Exclusion Criteria:

1. Subject has signs of or is diagnosed with Type 1 diabetes mellitus or latent autoimmune diabetes in adults.

2. History of hospitalizations or emergency room visits that would impact subject safety or data interpretation, including:

   • Poor glucose control in the 6 months prior to Screening (per investigator discretion) or
   • Any bariatric surgical procedures for weight loss.
3. History of significant change of body weight (> 10%) in the 3 months prior to Screening.
4. History of or active proliferative retinopathy or maculopathy within the 6 months before Screening or requiring acute treatment, or severe neuropathy.
5. History of previous gastrointestinal bleeding or ulceration within 3 months prior to Screening.
6. History of acute or chronic pancreatitis.

7. History of significant cardiovascular events defined as:

   • Myocardial infarction, coronary angioplasty or bypass grafts, valvular disease or repair, unstable angina pectoris, transient ischemic attack, or cerebrovascular accidents within 6 months prior to Screening.
   • Congestive heart failure defined as New York Heart Association (NYHA) Stages III and IV.
   • Uncontrolled hypertension defined as a systolic blood pressure > 160 mmHg and/or a diastolic blood pressure > 100 mmHg.
   • Symptomatic postural hypotension - The difference between supine blood pressure and standing blood pressure is 20 mmHg in systolic or 10 mmHg in diastolic with any symptom.
8. Evidence of uncorrected hypothyroidism or hyperthyroidism based on clinical evaluation and/or an abnormal thyroid stimulating hormone result as determined at Screening; subjects receiving dose-stable thyroid replacement therapy for at least 3 months prior to Screening will be allowed to participate in the study.
9. History of significant other major or unstable neurological, metabolic, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, or urological disorder that would impact subject safety or data interpretation.
10. History of cancer, other than squamous cell or basal cell carcinoma of the skin, that has not been in full remission for at least 5 years prior to Screening ( subjects with a history of treated cervical intraepithelial neoplasia will be allowed to participate in the study).
11. Active liver disease and/or significant abnormal liver function defined as aspartate aminotransferase (AST) > 2.5 × upper limit of normal (ULN) and/or alanine aminotransferase (ALT) > 2.5 × ULN and/or total bilirubin > 2.0 mg/dL.
12. Positive blood screen for anti-hepatitis C virus (HCV) antibody, hepatitis B surface antigen (HBsAg), and human immunodeficiency (HIV) antibody.
13. Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, ECG, or clinical laboratory assessments.
14. Long QT syndrome or prolongation of QTc interval (defined as QTc interval > 460 ms for males and > 480 ms for females).

15. The following medication exclusions apply:

    • Use of weight control treatment 3 months prior to Screening, including any medication with a labeled reference to weight loss or gain, herbal preparations, and over the counter medications.
    • Use of other anti-diabetic agents (except metformin) within 3 months prior to Screening (if the subject was previously treated with thiazolidinedione, he/she must have stopped this treatment at least 6 months before Screening).
    • Use of insulin within 12 months prior to Screening (the following cases can be included in this study: Insulin treatment during hospitalization, insulin treatment for a medical condition that did not require hospitalization [< 2 weeks treatment period], or insulin treatment for gestational diabetes).
16. Treatment with an investigational agent within the longest time frame of either 5 half lives or 30 days of initiating study drug.

17. Use of prohibited concomitant medications (further details about prohibited medication are provided in Section 5.8.1):

    • Current use of hyperglycemia-causing agents, hypoglycemia-causing agents, Class II and III antiarrhythmic agents (these agents will be allowed if they have been used for hypertension treatment), agents that reduce gastrointestinal motility, central nervous system stimulants (with the exception of caffeinated beverages), and niacin ≥ 1 g/day.
    • Current use of drugs with a narrow therapeutic index (eg, digoxin, lithium, phenytoin, theophylline, and warfarin).
    • Current use of drugs that are known to prolong the QT interval.
18. Known recreational substance use or psychiatric illness that, in the opinion of the Investigator, may impact the safety of the subject or the study objectives (eg, cannot comply with scheduled study visits).
19. History of drug abuse.
20. Women who are pregnant (confirmed by laboratory testing), nursing or are planning to become pregnant.
21. Subject is not willing to use an "effective" method of contraception during the course of the study. Sexually active male subjects are required to use a condom, abstain from intercourse, or previously undergone male sterilization. Male subjects should refrain from sperm donation for the purposes of conception for at least 90 days after their last dose of study drug. Females subjects must be surgically sterile (ie, hysterectomy or bilateral tubal ligation), postmenopausal, or for women of childbearing potential using a medically acceptable method of contraception (ie, intrauterine device, barrier methods with spermicide or abstinence). Female subjects of childbearing potential taking stable oral, implantable, or injectable contraceptives must additionally use a double-barrier method of contraception.
22. Subject has an FPG ≥ 270 mg/dL at the Screening visit.
23. Has a serum creatinine above (or creatinine clearance below) what is approved in the metformin product labeling in the respective country.
24. Known allergy or hypersensitivity to MLR-1023 or components of the formulation.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: MLR-1023 25mg QD; MLR-1023 25mg QD Tablet	Drug: MLR-1023; MLR-1023 Tablets
Experimental: MLR-1023 50mg QD; MLR-1023 50mg QD Tablet	Drug: MLR-1023; MLR-1023 Tablets
Experimental: MLR-1023 100mg QD; MLR-1023 100mg QD Tablet	Drug: MLR-1023; MLR-1023 Tablets
Placebo Comparator: Placebo; Placebo QDTablet	Other: Placebo; Matching Placebo Tablets

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes in HbA1c between active treatment groups and placebo at Week 12	Change in HbA1c from Baseline to Week 12	12 Weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
HbA1c of < 7.0% at Week 12	Proportion of Subjects with HbA1c of < 7.0% at Week 12	12 Weeks
HbA1c of < 6.5% at Week 12	Proportion of Subjects with HbA1c of < 6.5% at Week 12	12 Weeks
Changes in Fasting Plasma Glucose (FPG) from Baseline to Week 12 between active treatment groups and placebo	Changes in FPG from Baseline to Week 12	12 Weeks
Changes in fasting insulin, insulin sensitivities (HOMA IR)	Changes in fasting insulin, insulin sensitivities (HOMA IR) from Baseline to Week 12	12 Weeks
Changes in lipid profile (low density lipoprotein cholesterol [LDL-C], high density lipoprotein cholesterol [HDL-C], triglycerides)	Changes in lipid profile (low density lipoprotein cholesterol [LDL-C], high density lipoprotein cholesterol [HDL-C], triglycerides) from Baseline to Week 12	12 Weeks
Changes in Body Weight	Changes in Body Weight from Baseline to Week 12	12 Weeks

Collaborators and Investigators

• Sponsor: Melior Pharmaceuticals
• Collaborators: Bukwang Pharmaceutical, Co., Ltd.
• Investigators: Study Director: Ramana Kuchibhatla, PhD, Melior Pharmaceuticals, Inc.

Study record dates

Study Major Dates

• Study Start (Actual): September 1, 2017
• Primary Completion (Anticipated): September 1, 2019
• Study Completion (Anticipated): September 1, 2019

Study Registration Dates

• First Submitted: August 25, 2017
• First Submitted That Met QC Criteria: September 8, 2017
• First Posted (Actual): September 12, 2017

Study Record Updates

• Last Update Posted (Actual): January 9, 2019
• Last Update Submitted That Met QC Criteria: January 8, 2019
• Last Verified: January 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Diabetes Mellitus; Diabetes Mellitus, Type 2
• Other Study ID Numbers: BK-MD-202

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No