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OpenTrials
Completed

NCT Number: NCT02405260

Add Glucokinase Activator to Target A1c

This trial is a multi-center, adaptive, randomized, double-blind, placebo- and active- controlled, parallel group, Phase 2 study in subjects with T2DM to evaluate the effect of TTP399 on HbA1c following administration for 6 months.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Mesa, Arizona, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A historical diagnosis of Type 2 Diabetes in accordance with the American Diabetes Association (ADA) guidelines, with diagnosis at least 6 months prior to Screening.
  • On a stable (for the last 3 months prior to screening) regimen of metformin monotherapy equivalent of at least 1000 mg once daily.
  • Males, females of childbearing potential (must have a negative pregnancy test and be willing to comply with protocol contraception), and females of non-childbearing potential.
  • Age 18 to 75 years, inclusive, at the time of screening.
  • HbA1c ≥7.0% and ≤9.5%.
  • Generally stable health without active infection or history of major surgery or significant injuries within the last year.

Exclusion criteria

  • Diagnosis of Type 1 diabetes mellitus, maturity-onset diabetes of the young, insulin-requiring Type 2 Diabetes, other unusual or rare forms of diabetes mellitus, or history of diabetic ketoacidosis.
  • Clinically significant abnormal lab values including eGFR <50ml/min/1.73m2, ALT, bilirubin or AST >1.5 X ULN, hypokalemia or other clinically significant electrolyte abnormality.
  • History of myocardial infarction, unstable angina, coronary revascularization, stroke, or transient ischemic attack within 2 years of screening.
  • Presence of symptomatic congestive heart failure.
  • History of cardiac arrhythmias requiring treatment or prophylaxis with drugs or devices during the last 2 years or any history of atrial fibrillation or flutter beyond a single short-term episode (e.g., lasting 1-2 days).
  • History or presence of a 2nd degree or greater atrioventricular block in the absence of a pacemaker.
  • A 12-lead ECG, from screening or baseline demonstrating QTcF interval >450 msec for males or >47 msec for females.
  • A family or personal history of long QT syndrome.
  • History of pancreatitis.
  • Persistent, uncontrolled hypertension.
  • Presence of chronic active hepatitis (hepatitis B, hepatitis C, nonalcoholic steatohepatitis [NASH]) and/or known liver cirrhosis.
  • Participation in any formal weight loss program, or fluctuation of > 5% in body weight, or having received medications approved for weight loss within 3 months prior to screening.
  • A positive pre-study drug screen.
  • Participation in a clinical trial and receipt of an investigational product within 30 days.
  • Have a history of drug abuse within 2 years of screening or a positive pre-screen drug screen.
  • Have a history of hypoglycemic episode requiring glucose, glucagon, or orange juice administered by someone other than the patient within 6 months prior to screening.
  • A history of excessive alcohol consumption within the last 2 years prior to screening
  • Mental or legal incapacitation.
  • Blood donation of approximately 1 pint (500 mL) within 8 weeks.
  • History of MEN-2 or family history of medullary thyroid cancer.
  • History of cancer, other than non-melanoma skin cancer, that required therapy in the 5 years prior study start.

Treatment and study plan

TTP399 400 mg

Drug

once daily

TTP399 800 mg

Drug

once daily

Sitagliptin 100 mg

Drug

once daily

Placebo

Drug

once daily

Primary outcomes

  1. Change in HbA1c (Glycosylated haemoglobin)

    Time frame: Day 1 to Day 168

Secondary outcomes

  1. HbA1c < 7% at 6 months

    Time frame: Day 1 to Day 168

  2. HbA1c < 6.5% at 6 months

    Time frame: Day 1 to Day 168

  3. Plasma Glucose Levels

    Time frame: Day 1 to Day 168

  4. Lipid Levels

    Time frame: Day 1 to Day 168

  5. Insulin Levels

    Time frame: Day 1 to Day 168

  6. Lactate Levels

    Time frame: Day 1 to Day 168

  7. C-peptide Levels

    Time frame: Day 1 to Day 168

  8. Glucagon Levels

    Time frame: Day 1 to Day 168

  9. Glucagon-like Peptide-1 Levels

    Time frame: Day 1 to Day 168

  10. Change in Body Weight

    Time frame: Day 1 to Day 168

  11. Adverse Events

    Time frame: Day 1 to Day 182

  12. Blood Pressure

    Time frame: Day 1 to Day 182

  13. Electrocardiogram Parameters

    Time frame: Day 1 to Day 182

  14. Hematology

    Time frame: Day 1 to Day 182

  15. Blood Chemistry

    Time frame: Day 1 to Day 182

  16. Urinalysis

    Time frame: Day 1 to Day 182

  17. Pulse

    Time frame: Day 1 to Day 182

Sponsors and collaborators

Lead sponsor

vTv Therapeutics

Industry

Registry information

Official study title

A Multi-Center, Adaptive Phase 2, Randomized, Double-Blind, Placebo- and Active-Controlled (Sitagliptin), Parallel Group Study to Evaluate the Safety and Efficacy of TTP399 Following 6 Months Administration in Subjects With Type 2 Diabetes Mellitus on A Stable Dose of Metformin

Acronym: AGATA

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Apr 1, 2015
Registry last updated
Feb 10, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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