MedPath

Safety and Efficacy Study of Metaglidasen in Type 2 Diabetes in Patients Suboptimally Controlled on Insulin

Phase 2
Completed
Conditions
Type 2 Diabetes
Interventions
Registration Number
NCT00353587
Lead Sponsor
CymaBay Therapeutics, Inc.
Brief Summary

This is a multicenter, randomized, double-blind, placebo- and active comparator-controlled phase 2/3 study of three dose levels of MBX-102 (200, 400, 600 mg) given orally to patients with type 2 diabetes receiving concomitant therapy with insulin. Eligible patients will be adults with type 2 diabetes who are taking intermediate- and/or long-acting insulin or pre-mixed (e.g., "70/30") insulin, or a combination of insulin and one or two non-TZD hypoglycemic agents including sulfonylurea, metformin, acrabose or Byetta, but who are poorly controlled on their existing therapy. Preference for enrollment will be given to patients on insulin monotherapy. Patients treated with a combination of insulin and other hypoglycemic agent(s) must be willing and able to discontinue and washout of the hypoglycemic agent(s) for the entire duration of the study (in toto, approximately 28 weeks). Patients who are taking fixed doses of a short-acting insulin (e.g., not a "sliding scale") in combination with intermediate-acting insulin may qualify for the study if both the patient and investigator are willing to either change to pre-mixed insulin (e.g., 70/30) or discontinue use of the short acting insulin for at least 26 weeks. Patients treated with a sliding scale of short-acting insulin will not be eligible for enrollment.

Detailed Description

This is a multicenter, randomized, double-blind, placebo- and active comparator-controlled phase 2/3 study of three dose levels of MBX-102 (200, 400, 600 mg) given orally to patients with type 2 diabetes receiving concomitant therapy with insulin. Eligible patients will be adults with type 2 diabetes who are taking intermediate- and/or long-acting insulin or pre-mixed (e.g., "70/30") insulin, or a combination of insulin and one or two non-TZD hypoglycemic agents including sulfonylurea, metformin, acrabose or Byetta, but who are poorly controlled on their existing therapy. Preference for enrollment will be given to patients on insulin monotherapy. Patients treated with a combination of insulin and other hypoglycemic agent(s) must be willing and able to discontinue and washout of the hypoglycemic agent(s) for the entire duration of the study (in toto, approximately 28 weeks). Patients who are taking fixed doses of a short-acting insulin (e.g., not a "sliding scale") in combination with intermediate-acting insulin may qualify for the study if both the patient and investigator are willing to either change to pre-mixed insulin (e.g., 70/30) or discontinue use of the short acting insulin for at least 26 weeks. Patients treated with a sliding scale of short-acting insulin will not be eligible for enrollment.

Following any insulin dose adjustment during the first few weeks of the study, insulin dose and regimen should remain constant for the duration of the study.

No stand alone (e.g., other than pre-mixed) short- or ultrashort-acting insulin and/or sliding scale will be allowed for the entire duration of the study.

A minimum of 400 patients will be randomized in this study (approximately 80 to each of the five treatment arms). Additional patients may be enrolled as appropriate to replace screen failures and drop-outs during the initial period of the study.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
396
Inclusion Criteria
  • Type 2 diabetes (as described by the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus24) treated with insulin alone (a stable dose of long and/or intermediate-acting insulin or pre-mixed insulin e.g., "70/30") ≥ 30 units/day for at least 3 months, but poorly controlled on their existing therapy
  • Or, patients treated with insulin (as above) in combination with non-TZD hypoglycemic agents (e.g., a sulfonylurea, metformin, acrabose, or Byetta for at least 3 months, but poorly controlled on their existing therapy
  • Or, patients treated with fixed doses of short-acting insulin in combination with intermediate-acting insulin for at least 3 months, but poorly controlled on their existing therapy
  • Patients in last 2 categories must be willing to discontinue the use of OHA and/or short-acting insulin (or change to pre-mixed insulin) for at least 26 weeks.
  • Male or female, 18-75 years of age
  • Provide informed consent and agree to comply with study requirements
  • Current monotherapy insulin dose regimen ≥ 30 units/day (stable for 8-week Run-in/stabilization Period); or patients who need insulin dose adjustment must have a stabilized dose ≥ 30 units/day. Patients must not have taken TZDs within 5 months of screening
  • All female patients must be surgically sterile, post-menopausal (at least 40 years of age with no history of menses for at least 2 years) or agree to use adequate contraception(s) that must include a barrier method (other methods may include oral contraceptives, double barrier methods, intra-uterine devices, or abstinence). Depo contraceptives are excluded
  • Female patients must not be pregnant or lactating
  • BMI 26-44 kg/m2
  • Hemoglobin A1c must be ≥7.5%, ≤11.5% at both Screening and Visit 4
  • Patients must have a FPG ≤ 220 mg/dl
  • Patients must have liver function tests ≤ 2X the upper limits of normal for AST, ALT, and bilirubin, and ≤ 2.5X the upper limits of normal for ALP and GGT
  • Patients must have serum creatinine ≤ 1.8 mg/dl for males and ≤ 1.5 mg/dl for females and BUN ≤ 40 mg/dl
  • Fecal occult blood test must be negative
  • All other clinical laboratory parameters must be within normal limits or considered not clinically significant for participation in this study, including: hematology, coagulation, other serum chemistry, and other urinalysis parameters
  • TSH must be ≤ 3x ULN and patient clinically euthyroid in opinion of investigator. If TSH is > ULN but ≤ 3x ULN, and patient is clinically euthyroid, FT4 should be drawn and must be WNL
  • Electrocardiogram (ECG) must be normal, or considered not clinically significant, for participation in this study
  • Patients must have a blood pressure ≤ 160/90 mm/hg including hypertensive patients controlled with medication
Exclusion Criteria

Patients will be excluded from study participation if any of the following applies:

  • History of diabetes secondary to pancreatitis or pancreatectomy
  • Requirement for short-acting insulin during the study
  • Weight loss > 10 pounds in the three months prior to study
  • History of TZD use (Actos or Avandia) within 5 months of Screening Visit
  • History of TZD discontinuation due to side effect or lack of efficacy
  • Prior history of endoscopically or radiographically documented peptic ulcer disease within last 5 years (unless patient had documented H. pylori infection with subsequent treatment and no recurrence)
  • Prior history of GI bleeding within last 5 years (except for hemorrhoids or perianal disease)
  • Known infection with the human immunodeficiency virus (HIV) or history of viral hepatitis type B or C
  • History of congestive heart failure within last 5 years (NYHA Class III-IV)
  • History of significant pulmonary disease, myocardial infarction, cerebrovascular accident, or nephrotic syndrome within last 1 year
  • Elevated creatine phosphokinase (> 2X the upper limits of normal)
  • Malignancy within the last 5 years (except resected basal cell carcinoma)
  • Ongoing active infection, as evidenced by symptoms such as temperature > 38.5° C and/or clinically significant elevation in WBC count (i.e., not asymptomatic colonization)
  • Change in treatment with lipid-lowering agent after screening visit
  • Current or expected requirement for anticoagulant therapy [except for low- dose (≤ 325 mg/d) aspirin]
  • Current or expected treatment with phenytoin
  • Current or anticipated treatment with non-steroidal anti-inflammatory drugs (i.e., naproxen, ibuprofen, Vioxx, Celebrex, indomethacin, etc.). However, patients may take aspirin < 325 mg/day for cardiovascular prophylaxis
  • Known hypersensitivity to NSAIDs
  • Treatment with any other investigational therapy within the 30 days prior to Screening Visit
  • History of illicit drug or alcohol abuse within last 1 year
  • Current or expected treatment with systemic corticosteroids (except topical, ophthalmic, intra-articular, or inhaled at a dose < 1600 μg/day)
  • Any other condition that compromises the ability of the patient to provide informed consent or to comply with the objectives and procedures of this protocol, as judged by the investigator.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MBX-102 200 mgMBX-102MBX-102 200 mg once daily for 16 weeks
MBX-102 400 mgMBX-102MBX-102 400 mg once daily for 16 weeks
MBX-102 600 mgMBX-102MBX-102 600 mg once daily for 16 weeks
Sugar PillPlaceboPlacebo comparator once daily for 16 weeks
ActosActosActos 30 mg once daily for 16 weeks
Primary Outcome Measures
NameTimeMethod
Evaluate effects of MBX-102 administered orally at doses of 200, 400 and 600 mg daily for 16 weeks, on glucose control, as measured by HbA1c
Evaluate safety of MBX-102 with particular emphasis on endpoints of weight gain and edema
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (67)

NEA Clinic

🇺🇸

Jonesboro, Arkansas, United States

Associated Pharmaceutical Research Center, Inc.

🇺🇸

Buena Park, California, United States

Radiant Research - Greer

🇺🇸

Greer, South Carolina, United States

Dallas Diabetes & Endocrine Center

🇺🇸

Dallas, Texas, United States

McGuire VA Medical Center

🇺🇸

Richmond, Virginia, United States

Consultorio Integral de Atencion al Diabetico (CIAD)

🇦🇷

Buenos Aires, Argentina

Fundacion CIDEA

🇦🇷

Buenos Aires, Argentina

Instituto Medico Especializado

🇦🇷

Buenos Aires, Argentina

Clinica Dleta Zarate

🇦🇷

Buenos Aires, Argentina

Hospital Privado de Comunidad

🇦🇷

Buenos Aires, Argentina

Hospital Thompson

🇦🇷

Buenos Aires, Argentina

Christian Medical College Hospital

🇮🇳

Vellore, India

Assaf Haroffe Medical Center

🇮🇱

Zrifin, Israel

Amrita Institute of Medical Sciences

🇮🇳

Cochin, Kerala, India

Sri Ramachandra Medical Centre

🇮🇳

Chennai, India

Rambam Medical Center

🇮🇱

Haifa, Israel

Hadassah University Hospital

🇮🇱

Jerusalem, Israel

Department of Endocrinology, Ziv Medical Center

🇮🇱

Safed, Israel

Zamenhoff Medical Center

🇮🇱

Tel-Aviv, Israel

Diacon Hospital

🇮🇳

Bangalore, India

KEM Hospital

🇮🇳

Pune, India

Mediheights Healthcare Pvt. Ltd.

🇮🇳

Mumbai, India

Endocrinology Institute, Haemek Medical Center

🇮🇱

Afula, Israel

Barzilai Medical Center

🇮🇱

Ashkelon, Israel

Soroka Medical Center

🇮🇱

BeEr-Sheva, Israel

Linn Medical Center

🇮🇱

Haifa, Israel

Andres Patron DO PA

🇺🇸

Pembroke Pines, Florida, United States

The Intermed Group

🇺🇸

Los Angeles, California, United States

LAC/USC Medical Center

🇺🇸

Los Angeles, California, United States

International Research Associates, LLC

🇺🇸

Miami, Florida, United States

Sterling Hospital

🇮🇳

Ahmedabad, India

Olive Branch Research

🇺🇸

Olive Branch, Mississippi, United States

Policlio Modelo de Cipoletti

🇦🇷

Rio Negro, Argentina

Optimed Research, LLC

🇺🇸

Columbus, Ohio, United States

Wolfson Medical Center

🇮🇱

Holon, Israel

Clalit Health Services

🇮🇱

Jerusalem, Israel

Kasturba Medical College Hospital

🇮🇳

Attavar, Mangalore, India

St. John's Medical College Hospital

🇮🇳

Bangalore, India

M.S. Ramaih Medical College & Hospital

🇮🇳

Bangalore, India

Institution of Diabetes and Metabolism

🇮🇱

Nahariya, Israel

Endocrinology & Diabetes Institute

🇮🇱

Petach Tikva, Israel

CER San Juan Centro Polivalente de Asistencia e Investigacion Clinica

🇦🇷

San Juan Capital, Argentina

Diabetes Care and Research Center

🇮🇳

Maharashtra, India

Chowpatty Medical Center

🇮🇳

Mumbai, India

Kerala Institute of Medical Sciences

🇮🇳

Trivandrum, India

Dr. V. Seshiah Diabetes Care & Research Institute

🇮🇳

Chennai, India

Apollo Gleneages/Dept. of Endocrinology

🇮🇳

Kolkata, India

Institute of Metabolic Diseases

🇮🇱

Tel Aviv, Israel

Consultorios Asociados de Endocrinologia

🇦🇷

Capital Federal, Argentina

Instituto Latinoamericano de Investigaciones Clinicas

🇦🇷

Cordoba, Argentina

Sanatorio Parque

🇦🇷

Cordoba, Argentina

Kasturba Hospital

🇮🇳

Manipal, India

Nizam's Institute of Medical Sciences

🇮🇳

Panjagutta, Hyderabad, Andhra Pradesh, India

CIMEL

🇦🇷

Buenos Aires, Argentina

Centro de Atencion Integral en Diabetes, Endocrinologica y Metabolismo

🇦🇷

Buenos Aires, Argentina

Sanatorio Municipal Dr. Julio Mendez

🇦🇷

Buenos Aires, Argentina

Fundacion Marcelino Rusculleda Batlle

🇦🇷

Cordoba, Argentina

Instituto de Clinica Medica y Diabetes

🇦🇷

Mendoza, Argentina

Hospital San Bernardo

🇦🇷

Salta, Argentina

Mercury Pharma Services

🇺🇸

Houston, Texas, United States

Diabetes Center of the Southwest

🇺🇸

Midland, Texas, United States

Suncoast Clinical Research, Inc.

🇺🇸

Palm Harbor, Florida, United States

Diabetes & Glandular Disease Research Associates, P.A.

🇺🇸

San Antonio, Texas, United States

National Clinical Research

🇺🇸

Richmond, Virginia, United States

Clinical Investigation Specialists, Inc.

🇺🇸

Gurnee, Illinois, United States

Cedar-Crosse Research Center

🇺🇸

Chicago, Illinois, United States

Bharti Research Institute of Diabetes & Endocrinology

🇮🇳

Karnal, Haryana, India

© Copyright 2025. All Rights Reserved by MedPath