Current partner codePEPTIDESDE
NCT02752828·Phase 3·INTERVENTIONAL

Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination (LixiLan) to Insulin Glargine Alone on Top of Oral Anti-diabetic Drugs (OADs) With Type 2 Diabetes in Japan

Status

Completed

Phase

Phase 3

Enrollment

521

Locations

113

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

Primary Objective: To compare LixiLan to insulin glargine in glycated hemoglobin (HbA1c) change from baseline to Week 26 in patients with type 2 Diabetes. Secondary Objective: To compare the overall efficacy and safety of LixiLan to insulin glargine (with or without OADs) over a 26 Week treatment period in patients with type 2 Diabetes.

Full detailed description

The maximum study duration per patient will be approximately 29 weeks: an up to 2-week screening period, a 26-week randomized open-label treatment period and a 3-day post-treatment safety follow up period.

Interventions

Treatment arms and agents.

DRUG

Insulin glargine/lixisenatide (HOE901/AVE0010)

Pharmaceutical form: solution Route of administration: subcutaneous

DRUG

Insulin glargine (HOE901)

Pharmaceutical form: solution Route of administration: subcutaneous

DRUG

Oral anti-diabetic drugs

Pharmaceutical form: tablet Route of administration: oral

Timeline

From registration to results.

  1. First posted

    Apr 27, 2016

  2. Study start

    May 23, 2016

  3. Primary completion

    Mar 12, 2018

  4. Study completion

    Mar 12, 2018

  5. Results posted

    Not reported

  6. Registry updated

    Jun 16, 2020

Outcomes

What the study measures.

Primary outcomes

Change from baseline in HbA1c

Time frame · Baseline, 26 weeks

Secondary outcomes

Percentage of patients reaching HbA1c <7% or ≤6.5%

Time frame · 26 weeks

Change from baseline in 2-hour postprandial glucose (PPG) during standardized meal test

Time frame · Baseline, 26 weeks

Change from baseline in 7 point self monitored plasma glucose (SMPG) profiles during standardized meal test

Time frame · Baseline, 26 weeks

Change from baseline in body weight

Time frame · Baseline, 26 weeks

Percentage of patients reaching HbA1c <7% with no body weight gain and with no documented (PG ≤70 mg/dL [3.9 mmol/L]) symptomatic hypoglycemia

Time frame · 26 weeks

Percentage of patients reaching HbA1c <7% at Week 26 with no documented (PG ≤70 mg/dL [3.9 mmol/L]) symptomatic hypoglycemia

Time frame · 26 weeks

Percentage of patients requiring a rescue therapy

Time frame · 26 weeks

Number of adverse events

Time frame · 26 weeks

Number of hypoglycemic events

Time frame · 26 weeks

Measurement of anti-lixisenatide antibodies from baseline

Time frame · Baseline, 26 weeks

Eligibility

Who can take part.

Minimum age
20 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion criteria : * Patient with type 2 diabetes mellitus (T2DM) diagnosed for at least 1 year before the screening visit, receiving 1 or 2 OADs that can be Biguanide,Thiazolidinedione (TZD), -Alpha-glucosidase-inhibitor (alpha-GI),Sodium glucose co-transporter 2 (SGLT2) inhibitor,Sulfonylurea (SU),Rapid-acting insulin secretagogue (Glinide),diphenyl-peptidase -4 inhibitor (DPP-4 inhibitor). * Signed written informed consent. Exclusion criteria: * At the screening visit: Age \<20 years. * At the screening visit: HbA1c \<7.5% or \>9.5%. * At the screening visit: fasting plasma glucose (FPG) \>180 mg/dL (10.0 mmol/L). * Pregnancy or lactation, women of childbearing potential with no effective contraceptive method. * Use of oral or injectable glucose-lowering agents other than those stated during the inclusion criteria in the 3 months before the screening visit. * Previous treatment with insulin (except for short-term treatment due to intercurrent illness including gestational diabetes at the discretion of the trial physician). * Laboratory findings at the time of screening: * Amylase and/or lipase: \>3 times the upper limit of the normal (ULN) laboratory range, * Alanine aminotransferase (ALT) or aspartate aminotransferase (AST): \>3 ULN, * Calcitonin ≥20 pg/mL (5.9 pmol/L), * Positive serum pregnancy test in female of childbearing potential. * Contraindication to use of lixisenatide according to the local labeling. History of hypersensitivity to any Glucagon-Like Peptide-1 Receptor Agonists or to metacresol. * Contraindication to use of insulin glargine according to local labeling. History of hypersensitivity to insulin glargine or to any of the excipients. * Patient who has a severe renal function impairment with estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m\^2 or end-stage renal disease for patient not treated with metformin. * Personal or immediate family history of medullary thyroid cancer (MTC) or genetic condition that predisposes to MTC (eg, multiple endocrine neoplasia syndromes). * History of pancreatitis (unless pancreatitis was related to gallstones and cholecystectomy has been performed), pancreatitis during previous treatment with incretin therapies, chronic pancreatitis, pancreatectomy, stomach/gastric surgery. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study locations

113 registered sites.

Japan. Showing up to 24 locations stored in the fast local snapshot.

Investigational Site Number 392002

Adachi-Ku, Japan

Investigational Site Number 392132

Annaka-Shi, Japan

Investigational Site Number 392009

Arakawa-Ku, Japan

Investigational Site Number 392025

Atsugi-Shi, Japan

Investigational Site Number 392024

Chiba, Japan

Investigational Site Number 392151

Chiba, Japan

Investigational Site Number 392011

Chigasaki-Shi, Japan

Investigational Site Number 392013

Chiyoda-Ku, Japan

Investigational Site Number 392052

Chiyoda-Ku, Japan

Investigational Site Number 392003

Chūōku, Japan

Investigational Site Number 392017

Chūōku, Japan

Investigational Site Number 392055

Chūōku, Japan

Investigational Site Number 392155

Chūōku, Japan

Investigational Site Number 392008

Fujimi-Shi, Japan

Investigational Site Number 392143

Fujisawa-Shi, Japan

Investigational Site Number 392054

Fukuoka, Japan

Investigational Site Number 392094

Fukuoka, Japan

Investigational Site Number 392147

Fukuoka, Japan

Investigational Site Number 392100

Gifu, Japan

Investigational Site Number 392059

Hachioji-Shi, Japan

Investigational Site Number 392083

Hakodate-Shi, Japan

Investigational Site Number 392048

Hamamatsu, Japan

Investigational Site Number 392102

Hamamatsu, Japan

Investigational Site Number 392079

Hiki-Gun, Japan

Related trials

More studies on Lixisenatide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.