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Single Ascending Dose Trial in Patients With Type 2 Diabetes

This study has been terminated.
(Decision by Sponsor)
Information provided by (Responsible Party):
Amgen Identifier:
First received: September 28, 2011
Last updated: February 13, 2013
Last verified: February 2013

September 28, 2011
February 13, 2013
November 2011
July 2012   (Final data collection date for primary outcome measure)
  • Subject incidence of treatment-emergent adverse events [ Time Frame: 29 days ]
    Physical examinations, vitals, clinical laboratories, and ECGs
  • Safety laboratory analytes, vital signs, and ECGs [ Time Frame: 29 days ]
    laboratory analytes, vital signs, and ECGs
  • Subject incidence of anti-AMG 876 antibodies. [ Time Frame: 29 days ]
    laboratories analytes
Same as current
Complete list of historical versions of study NCT01492465 on Archive Site
  • AMG 876 serum PK parameters [ Time Frame: 29 days ]
    Concentration-time profiles for AMG 876
  • Pharmacodynamic parameters: [ Time Frame: 29 days ]
    Concentration of fasting glucose, insulin and c-peptide levels; Concentration-time profiles and AUC for metabolic parameters (eg, glucose, insulin, c-peptide, glucagon and free fatty acid concentrations) following a mixed meal tolerance test; Lipid levels (ie, total cholesterol, LDL, HDL, and triglycerides); Body weight.
Same as current
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Single Ascending Dose Trial in Patients With Type 2 Diabetes
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Ascending Single Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 876 in Subjects With Type 2 Diabetes
The purpose of this study is to determine whether AMG 876 is safe and well tolerated in subjects with type 2 diabetes.
Not Provided
Phase 1
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Diabetes Mellitus
Drug: AMG 876
Ascending single doses of study drug administered SC, with one cohort administered IV
  • Active Comparator: AMG 876
    Intervention: Drug: AMG 876
  • Placebo Comparator: Placebo
    Intervention: Drug: AMG 876
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
October 2012
July 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Subject has provided written informed consent
  • Men and women between the ages of 18 and 65, inclusive at the time of randomization
  • Women must be of documented non-reproductive potential (ie, postmenopausal [see definition below]; OR history of hysterectomy; OR history of bilateral tubal ligation; OR history of bilateral oophorectomy).
  • Diagnosed with type 2 diabetes
  • HbA1c ≥ 6.5% and ≤ 10%
  • Fasting C-peptide value ≥ 0.8 ng/mL
  • Men must agree for the duration of the study and continuing for 4 weeks after the dose of study drug, to practice a highly effective method of birth control. Highly effective methods of birth control include sexual abstinence, vasectomy or a condom with spermicide (men) in combination with either barrier methods, hormonal birth control or IUD (women).
  • Men must agree to not donate sperm for the duration of the study and continuing for 4 weeks after the dose of study drug.
  • Body mass index between ≥ 25.0 kg/m2 and ≤ 40.0 kg/m2 at screening
  • Negative screening test for alcohol and potential drugs of abuse at screening and day -2, unless medication is prescribed by a physician and approved by the principal investigator and Amgen medical monitor

Exclusion Criteria:

  • Men with partners who are pregnant at the time of screening or men with partners who plan to become pregnant during the study
  • Women who are pregnant or breastfeeding History or evidence of a clinically significant disorder, condition or disease that, in the opinion of the principal investigator or Amgen medical monitor would pose a risk to subject safety or interfere with the study evaluation, procedures or completion
  • Evidence or history at screening of diabetic complications with significant end-organ damage, eg, proliferative retinopathy and/or macular edema, creatinine clearance < 60 mL/min/1.73m2 (calculated using the Modification of Diet in Renal Disease formula), or macroalbuminuria (ie, ≥ +1 proteinuria on urinalysis), diabetic neuropathy complicated by neuropathic ulcers, or severe autonomic neuropathy with gastroparesis, chronic diarrhea, or hypoglycemic unawareness
  • Significant cardiac disease, including but not limited to evidence or history of coronary artery disease, unstable angina, congestive heart failure, known arrhythmias of ventricular etiology, unexplained syncope or syncope/seizures related to arrhythmia
  • Positive for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (Hbs Ag), or hepatitis C virus antibodies
  • An unstable medical condition, defined as having been hospitalized within 28 days before day -1, major surgery within 6 months before day -1, or otherwise unstable in the judgment of the investigator (eg, risk of complications or adverse events unrelated to study participation)
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
United States
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Study Director: MD Amgen
February 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP