Suspended

LIK066 Monotherapy Efficacy and Safety in Type 2 Diabetes

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Study Aim

This phase 2 study aims to evaluate the safety and effectiveness of LIK066 as a standalone treatment for Type 2 Diabetes, specifically measuring changes in glycated hemoglobin (HbA1c) levels after 12 weeks of treatment.

What is being tested

LIK066

+ LIK066

+ LIK066

Drug
Who is being recruted

Diabetes Mellitus+3

+ Endocrine System Diseases

+ Metabolic Diseases

From 18 to 75 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-ControlledPhase 2
Interventional
Study Start: November 2015
See protocol details

Summary

Principal SponsorNovartis Pharmaceuticals
Last updated: April 3, 2014
Sourced from a government-validated database.Claim as a partner

Study start date: November 1, 2015

Actual date on which the first participant was enrolled.

The purpose of the study is to evaluate the efficacy, tolerability and short-term safety of LIK066 to support dose selection for phase 3.

NCT01824264
Principal SponsorNovartis Pharmaceuticals
Last updated: April 3, 2014
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 75 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Diabetes MellitusEndocrine System DiseasesMetabolic DiseasesNutritional and Metabolic DiseasesGlucose Metabolism DisordersDiabetes Mellitus, Type 2

Criteria

Inclusion Criteria: Confirmed diagnosis of T2DM by standard criteria Drug-naïve patients, defined as patients not having received any anti-diabetic medication previously, Currently untreated patients , who, after the diagnosis of T2DM, have received anti-diabetic medication for not more than 12 consecutive weeks, and have not received any anti-diabetic treatment within 12 weeks prior to Visit 1 Patients being treated with mono-therapy for at least 8 consecutive weeks prior to Visit 1 with the following OADs: metformin, dipeptidyl peptidase-4 inhibitors (DPP-4i), SU, glinide, alpha-glucosidase inhibitor (AGI) HbA1c ≥ 7 to ≤ 10.5% at Visit 1 for drug-naïve/currently untreated patients HbA1c ≥ 7 to ≤ 9.5% at Visit 1 for patients treated with OAD monotherapy HbA1c ≥ 7 to ≤ 10.5% at Visit 199 for ALL patients Age: ≥18 and ≤ 75 years old at Visit 1 BMI ≥22 to ≤45 kg/m2 at Visit 1 Exclusion Criteria: FPG ≥270 mg/dl (15 mmol/L) for drug-naïve/currently untreated patients or ≥240 mg/dl (13.3 mmol/L) for patients on OAD monotherapy at Visit 1 Insulin treatment >4 consecutive weeks in the last 6 months, corticosteroid use >7 days in the last 8 weeks, use of growth hormones in the last 6 months, or use of weight control products > 4 weeks in the last 6 months History of acute metabolic complications, CV disease, type 1 diabetes mellitus, hepatic disorders, pancreatitis, chronic diarrhea Significant lab abnormalities such as TSH outside of normal range, UACR>300 mg/g creatinine, eGFR <60 ml/min/1.73m2, hemoglobin <12 g/L in men and <11 g/L in women, hematuria ECG abnormalities including AV block, long QT syndrome or QTc>450 msec for men and >470 msec for women History of malignancy Women of child-bearing potential not using effective methods of contraception Other protocol-defined inclusion/exclusion criteria may apply

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

9 intervention groups are designated in this study

11.111% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
Patients receive 2.5 mg of LIK066 once daily for 12 weeks

Group II

Experimental
Patients receive 5 mg of LIK066 once daily for 12 weeks

Group III

Experimental
Patients receive 10 mg of LIK066 once daily for 12 weeks

Group IV

Experimental
Patients receive 25 mg of LIK066 once daily for 12 weeks

Group 5

Experimental
Patients receive 50 mg of LIK066 once daily for 12 weeks

Group 6

Experimental
Patients receive 100 mg of LIK066 once daily for 12 weeks

Group 7

Experimental
Patients receive 150 mg of LIK066 once daily for 12 weeks

Group 8

Active Comparator
Patients receive 100 mg sitagliptin once daily for 12 weeks

Group 9

Placebo
Patients receive placebo for 12 weeks

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has no location dataSave this study to your profile to know when the location data is available.
SuspendedNo study centers