A Study on Safety, Pharmacokinetics and Pharmacodynamics of Lixisenatide in Pediatric Patients With Type 2 Diabetes Mellitus (T2DM)

Completed · Phase 1 · Has a placebo group

Conditions studied: Type 2 Diabetes Mellitus

In brief

Primary Objective: To demonstrate safety of 14-day repeated lixisenatide doses with 3 ascending doses as compared to placebo in pediatric patients with T2DM. Secondary Objectives: * To evaluate plasma concentrations of lixisenatide after repeated doses (3 ascending doses) and pharmacokinetic parameters of repeated lixisenatide doses in pediatric patients with T2DM. * To evaluate the change from baseline in fasting and post-prandial plasma glucose concentrations during a standardized meal test after 3 ascending repeated doses of lixisenatide in comparison to placebo.

Key facts

Study ID

NCT02803918

Run by

Sanofi

People needed

23

Starts

2017-05-17

Expected to finish

2020-01-27

Last updated by the study team

2022-04-25

Who can join

Age: 10 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female patients aged ≥10 and <18 years old (at least 4 patients below 16 years old).
• Body mass index (BMI) >85th percentile for age and gender; BMI ≤50 kg/m2.
• Male and female patients with documented T2DM insufficiently controlled with metformin at a stable dose and regimen for 8 weeks prior to randomization and/or basal insulin at stable dose (± 20%) and regimen for 8 weeks prior to randomization. The exact individual metformin dose will be selected according to local regulation and to the investigator's medical judgment.
• Glycated hemoglobin (HbA1c) >6.5% and ≤11% at screening.

You may not qualify if…

• If female, ongoing pregnancy (defined as positive serum pregnancy test), breast-feeding.
• Sexually active postmenarchal female patient who does not agree to use an adequate and highly effective method of contraception throughout the study duration and according to local regulation (ie, hormonal contraception, condom, etc.).
• Diabetes other than T2DM.
• Fasting plasma glucose >250 mg/dL (>13.9 mmol/L) at screening.
• Use of other oral or injectable antidiabetic or hypoglycemic agents other than metformin and basal insulin (eg, alpha glucosidase inhibitor, glucagon-like peptide (GLP-1) receptor agonist, dipeptidyl peptidase-IV (DPP-IV) inhibitors, short-acting insulin etc.) within 1 month prior to the screening visit.
• History of unexplained pancreatitis, chronic pancreatitis, pancreatectomy, stomach/gastric surgery, inflammatory bowel disease.
• The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Where it is running

• Investigational Site Number 840002 — Baton Rouge, Louisiana, United States
• Investigational Site Number 840006 — New Orleans, Louisiana, United States
• Investigational Site Number 840009 — Philadelphia, Pennsylvania, United States
• Investigational Site Number 840007 — Lufkin, Texas, United States
• Investigational Site Number 480001 — Phoenix, Mauritius
• Investigational Site Number 484001 — Monterrey, Mexico
• Investigational Site Number 484002 — Puebla City, Mexico
• Investigational Site Number 710001 — Cape Town, South Africa
• Investigational Site Number 724002 — Barcelona, Spain
• Investigational Site Number 792002 — Ankara, Turkey (Türkiye)
• Investigational Site Number 792001 — Izmir, Turkey (Türkiye)

Full record on ClinicalTrials.gov

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