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Phase 1 Completed N=142 Randomized Double-blind Basic Science

A Study of Tirzepatide (LY3298176) in Healthy Participants and Participants With Type 2 Diabetes (T2DM)

Healthy · Type 2 Diabetes Mellitus (T2DM)
Source: ClinicalTrials.gov NCT02759107 ↗
Enrolled (actual)
142
Serious AEs
0.7%
Results posted
Jan 2024
Primary outcomePrimary: Number of Participants With One or More Serious Adverse Event(s) (SAEs) — 0; 0; 0; 0 Participants

Summary

The main purposes of this study are to determine: * The safety of tirzepatide and any side effects that might be associated with it. * How much tirzepatide gets into the bloodstream and how long it takes the body to get rid of it. * How tirzepatide affects the levels of blood sugar. This study includes 3 parts (A, B and C). Part A involves a single dose of tirzepatide taken as a subcutaneous (SC) injection just under the skin and will be approximately 10 weeks in duration, including screening. Parts B and C involve 4 doses of tirzepatide taken once weekly (over 4 weeks) as a SC injection just under the skin and is approximately 12-14 weeks in duration, including screening. Each participant will enroll in only one part. This study is for research purposes only, and is not intended to treat any medical condition.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With One or More Serious Adverse Event(s) (SAEs)
0; 0; 0; 0; 1; 0
SECONDARY
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Tirzepatide in Part A.
5760; 12000; 22600; 53200; 90500; 169000
SECONDARY
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Tirzepatide in Part B
6000; 16300; 53300; 56900
SECONDARY
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Tirzepatide in Part C
4770; 50500; 41900; 37990
SECONDARY
Pharmacodynamics (PD): Ratio of AUC of Glucose on Day 2 to Baseline (Part C)
0.99; 0.72; 0.65; 0.73
SECONDARY
Pharmacodynamics (PD): Ratio of AUC of Glucose on Day 23 to Baseline (Part C)
0.96; 0.61; 0.58; 0.57

Eligibility Criteria

Inclusion Criteria

  • Healthy participants (Parts A and B) and participants with T2DM diagnosed at least 1 year before enrollment (Part C)
  • Have a screening body mass index (BMI) of greater than 18.5 and less than or equal to 40.0 kilograms per meter squared (kg/m²), inclusive
  • Participants with T2DM (Part C only): have T2DM controlled with diet and exercise alone or are stable on a single oral antidiabetic medication (metformin for at least 30 days or sulfonylureas). Participants receiving sulfonylureas may participate only if this treatment is stopped for at least 6 weeks before dosing with study drug

Exclusion Criteria

  • Have known allergies to tirzepatide, glucagon-like peptide (GLP)-1 analogs, or related compounds
  • Have an abnormality in the 12-lead electrocardiogram (ECG) at screening that, in the opinion of the investigator, increases the risks associated with participating in the study
  • Have a history or presence of pancreatitis (history of chronic pancreatitis or idiopathic acute pancreatitis), elevation in serum amylase or lipase (greater than 2-fold the upper limit of normal [ULN]) or gastrointestinal (GI) disorder (for example, relevant esophageal reflux or gall bladder disease) or any GI disease which impacts gastric emptying (for example, gastric bypass surgery, pyloric stenosis, with the exception of appendectomy) or could be aggravated by glucagon-like peptide-1 (GLP-1) analogs or dipeptidyl peptidase (DPP)-IV inhibitors

Participants with T2DM (Part C only)

  • Have had more than 1 episode of severe hypoglycemia, as defined by the American Diabetes Association criteria, within 6 months before entry into the study or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms

All Study Participants (Parts B and C only)

  • have known allergies to tirzepatide, GLP-1 analogs, or related compounds, or acetaminophen
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02759107). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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