Current partner codePEPTIDESDE
NCT03529123·Phase 3·INTERVENTIONAL

Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination Versus Insulin Glargine in Patients With Type 2 Diabetes (LixiLan-India)

Status

Completed

Phase

Phase 3

Enrollment

247

Locations

13

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Primary Objective: To demonstrate the superiority of the insulin glargine/lixisenatide fixed ratio combination (FRC) to insulin glargine by demonstrating change in glycosylated hemoglobin (HbA1c). Secondary Objectives: * To assess the effects of the FRC in comparison with insulin glargine on: * Percentage of patients reaching HbA1c targets (\<7% ); * Glycemic control in relation to a meal as evaluated by 2-hour Post-prandial Plasma Glucose; (PPG); * Body weight * Fasting Plasma Glucose (FPG); * Percentage of patients reaching HbA1c targets of \<7% with no body weight gain and no hypoglycemia (as defined in the evaluation criteria); * 7-point Self-Monitoring Plasma Glucose (SMPG) profile; * Insulin glargine dose. * To assess the safety and tolerability in each treatment group.

Full detailed description

The maximum study duration per patient is 33 weeks.

Interventions

Treatment arms and agents.

DRUG

INSULIN GLARGINE/LIXISENATIDE (HOE901/AVE0010)

Pharmaceutical form: Injection Route of administration: Subcutaneous

DRUG

INSULIN GLARGINE (HOE901)

Pharmaceutical form: Injection Route of administration: Subcutaneous

DRUG

Metformin

Pharmaceutical form: Tablet Route of administration: Oral

DRUG

Insulin Glulisine (HMR1964)

Pharmaceutical form: Injection Route of administration: Subcutaneous

Timeline

From registration to results.

  1. First posted

    May 18, 2018

  2. Study start

    Jun 19, 2018

  3. Primary completion

    Nov 25, 2019

  4. Study completion

    Nov 25, 2019

  5. Results posted

    Not reported

  6. Registry updated

    Apr 25, 2022

Outcomes

What the study measures.

Primary outcomes

Change in HbA1c

Time frame · From baseline to Week 24

Mean change in glycosylated hemoglobin (HbA1c) from baseline to Week 24

Secondary outcomes

Patients with HbA1c <7%

Time frame · At Week 24

Number of patients reaching HbA1c \<7 % at the end of Week 24

Change in 2-hour Post prandial glucose (PPG)

Time frame · From baseline to Week 24

Change in 2-hour PPG from baseline to Week 24

Change in body weight

Time frame · From baseline to Week 24

Change in body weight from baseline to Week 24

Patients with HbA1c <7% with no body weight gain and no hypoglycemia

Time frame · At Week 24

Number of patients reaching HbA1c \<7% with no body weight gain and no hypoglycemia at the end of Week 24

Change in Fasting Plasma Glucose

Time frame · From baseline to Week 24

Mean change in FPG from baseline to Week 24

Adverse events (AE)

Time frame · Up to 33 weeks

Number of AEs

Patients with HbA1c <7% with no body weight gain

Time frame · At Week 24

Number of patients reaching HbA1c \<7% with no body weight gain at the end of Week 24

Change in SMPG profiles

Time frame · From baseline to Week 24

Change in 7-point self-monitoring plasma glucose (SMPG) profiles from baseline to Week 24

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
64 Years
Sex
ALL
Healthy volunteers
No

Inclusion criteria : * Patients with type 2 diabetes mellitus (T2DM) diagnosed for at least 1 year before the screening visit, * At screening: * Age should be ≥ 18 years of age to \< 65 years; * Glycosylated hemoglobin (HbA1c) at screening visit ≥ 7.5% or ≤ 10%; * Body mass index (BMI) ≥ 19 kg/m2 and ≤ 40 kg/m2. * Patients who have been treated with a basal insulin for at least 6 months before the screening visit, and who have been on a stable basal insulin regimen (ie, type of insulin and time/frequency of the injection), for at least 3 months before the screening visit. The stable total daily dose should be within the range of 15-40 U, both inclusive, on the day of screening, but individual fluctuations of ± 20% within 2 months prior to screening are acceptable. Exclusion criteria: * Use of oral or injectable glucose-lowering agents other than those stated in the inclusion criteria in the 3 months before screening. * Previous use of insulin regimen other than basal insulin eg, prandial or pre-mixed insulin (Note: Short term treatment due to intercurrent illness including gestational diabetes is allowed at the discretion of the investigator). * For patients taking metformin, any contraindication to metformin use, according to local labeling. * For patient not treated with metformin at screening: severe renal function impairment with an estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73m2 or end-stage renal disease. * Personal or immediate family history of medullary thyroid cancer (MTC) or genetic condition that predisposes to MTC (eg, multiple endocrine neoplasia syndromes). * Clinically relevant history of gastrointestinal disease associated with prolonged nausea and vomiting, including (but not limited to): gastroparesis, unstable (ie, worsening) or not controlled (ie, prolonged nausea and vomiting) gastroesophageal reflux disease requiring medical treatment, within 6 months prior to the time of screening visit; or history of surgery affecting gastric emptying. * History of pancreatitis (unless pancreatitis was related to gallstones and cholecystectomy has been performed), pancreatitis during previous treatment with incretin therapies, chronic pancreatitis, pancreatectomy. * Average insulin glargine daily dose \<20 U or \>50 U calculated for the last 3 days before Visit 6. * Amylase and/or lipase \>3 upper limit normal (ULN) at Visit 5 (Week -1). The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study locations

13 registered sites.

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

Investigational Site Number 01

Bangalore, India

Investigational Site Number 012

Belagavi, India

Investigational Site Number 013

Chennai, India

Investigational Site Number 017

Coimbatore, India

Investigational Site Number 06

Hyderabad, India

Investigational Site Number 07

Hyderabad, India

Investigational Site Number 08

Jaipur, India

Investigational Site Number 04

Kolkata, India

Investigational Site Number 018

Lucknow, India

Investigational Site Number 014

Madurai, India

Investigational Site Number 05

Nashik, India

Investigational Site Number 010

New Delhi, India

Investigational Site Number 016

Pune, India

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

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.