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Trial · Interventional

CompletedPhase 3Registry data

Efficacy and Safety of LixiLan Versus Insulin Glargine Alone Both With Metformin in Japanese With Type 2 Diabetes Mellitus Inadequately Controlled on Basal Insulin and Oral Antidiabetic Drugs

Short name LIXILAN JP-L

NCTNCT02752412 (opens ClinicalTrials.gov in a new tab)Other idEFC14113Other idU1111-1176-8378

Overview

Status
Completed
Phase
Phase 3
Enrollment
513 participants (actual)
Sponsor
Sanofi · Industry
Design
Randomized · Open label (no masking)
Countries
1 country

Japan

Start
17 May 2016
Primary completion
4 Oct 2018
Completion
4 Oct 2018
First posted
27 Apr 2016 (estimated)
Last update posted
16 Jun 2020
Conditions
Type 2 Diabetes Mellitus

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2016201720182019
  1. Ph 3

    LIXILAN JP-L

    NCT02752412

    17 May 2016 to 4 Oct 2018

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Primary Objective: To compare LixiLan to insulin glargine in glycated hemoglobin (HbA1c) change from baseline to week 26 in patients with type 2 diabetes mellitus. Secondary Objective: To compare overall efficacy and safety of LixiLan to insulin glargine over 26 weeks in patients with type 2 diabetes mellitus.

Interventions

  • Insulin glargine/Lixisenatide (HOE901/AVE0010)Drug
  • Insulin glargine U100 (HOE901)Drug
  • MetforminDrug

Arms2

  • Experimental

    LixiLan

    LixiLan (insulin glargine/lixisenatide fixed ratio combination) is injected subcutaneously (under the skin) once daily. Dose is individually adjusted. Metformin will be continued.

  • Active comparator

    insulin glargine

    Insulin glargine U100 (Lantus) will be injected subcutaneously (under skin) once daily. Dose will be individually adjusted. Metformin will be continued.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Change from baseline in HbA1c

    Time frame · Baseline, 26 weeks

Secondary outcomes(15)
  1. Percentage of patients reaching HbA1c <7% or ≤6.5%

    Time frame · 26 weeks

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

    Time frame · Baseline, 26 weeks

  3. Change from baseline in blood glucose excursion during standardized meal test

    Time frame · Baseline, 26 weeks

  4. Change from baseline in 7-point self-monitoring plasma glucose (SMPG) profiles (each time point and average daily value)

    Time frame · Baseline, 26 weeks

  5. Change from baseline in body weight

    Time frame · Baseline, 26 weeks

  6. Change from baseline in FPG

    Time frame · Baseline, 26 weeks

  7. Change from baseline in daily dose of insulin glargine

    Time frame · Baseline, 26 weeks

  8. Percentage of patients reaching HbA1c <7% with no body weight gain

    Time frame · 26 weeks

  9. 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

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

    Time frame · 26 weeks

  11. Percentage of patients requiring a rescue therapy

    Time frame · 26 weeks

  12. Number of hypoglycemic events

    Time frame · 26 weeks

  13. Number of adverse events

    Time frame · 26 weeks

  14. Measurement of anti-lixisenatide antibodies from baseline

    Time frame · Baseline, 26 weeks

  15. Measurement of anti-insulin antibodies from baseline

    Time frame · Baseline, 26 weeks

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Randomized controlled trial · 2020

6 results

Efficacy and safety of insulin glargine/lixisenatide fixed-ratio combination (iGlarLixi) in Japanese patients with type 2 diabetes mellitus inadequately controlled on basal insulin and oral antidiabetic drugs: The LixiLan JP-L randomized clinical trial.

Kaneto et al. 2020Diabetes, obesity & metabolismcited by 32

PMID 32072742DOI 10.1111/dom.14005PUB-32072742

Full text at the publisher6 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 20 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion criteria : * Patient with type 2 diabetes mellitus (T2DM) diagnosed for at least 1 year before the screening visit (V1). * Patient treated with a stable, once a day basal insulin regimen (ie, type of insulin and time/frequency of the injection), for at least 3 months before the screening visit. * The total daily basal insulin dose should be stable (± 20%) and \<15 U/day for at least 1 month before the screening visit. * Patient receiving 1 or 2 oral anti-diabetic drugs (OADs): the OAD dose(s) must be stable during the 3 months before the screening visit. The OADs can be 1 to 2 out of: * Metformin; * Sulfonylurea (SU); * Glinide; * Dipeptidyl-peptidase-4 (DPP-4) inhibitor; * Sodium glucose co-transporter 2 (SGLT2) inhibitor; * Alpha glucosidase inhibitor (alpha-GI). * Signed written informed consent. Exclusion criteria: * Age \<20 years at screening visit. * HbA1c at screening visit \<7.5% or \>9.5%. * Fasting plasma glucose (FPG) \>180 mg/dL (10.0 mmol/L) at screening visit. * Pregnancy or lactation, women of childbearing potential with no effective contraceptive method. * Use of oral or injectable glucose-lowering agents other than those stated in the inclusion criteria in the 3 months before screening visit. * Previous use of insulin regimen other than basal insulin, eg, prandial or pre-mixed insulin. Note: Short-term treatment (≤10 days) due to intercurrent illness including gestational diabetes is allowed at the discretion of the Investigator. * Use of thiazolidinedione (TZD) within 6 months prior to screening visit. * History of discontinuation of a previous treatment with a glucagon-like peptide-1(GLP-1) receptor agonist due to safety/ tolerability issues or lack of efficacy. * Laboratory findings at the screening visit; including: * 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. * Any contraindication to metformin use according to local labeling. * History of hypersensitivity to any GLP-1 receptor agonist or to metacresol. * Contraindication to use of insulin glargine or lixisenatide according to local labeling. History of hypersensitivity to insulin glargine or to any of the excipients. * 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 now been performed), pancreatitis during previous treatment with incretin therapies, chronic pancreatitis, pancreatectomy, stomach/gastric surgery. * Exclusion criteria for randomization at the end of the run-in phase: * HbA1c \<7.5% or \>9.5% at visit 6 (Week -1). * Mean fasting self monitored plasma glucose (SMPG) \>160 mg/dL (8.9 mmol/L), calculated from all available (minimum of 4 self-measurements) values during the 7 days prior to randomization. Note:fasting SMPG on the day of randomization can be included if assessed before randomization. * Average insulin glargine daily dose ≥15 U/day or \<5U/day calculated for the last 3 days before Visit 7. * Metformin total daily dose \<750 mg/day. * Amylase and/or lipase \>3 ULN at Visit 6 (Week -1). The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

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