LIK066 Monotherapy Efficacy and Safety in Type 2 Diabetes
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.
LIK066
+ LIK066
+ LIK066
Diabetes Mellitus+3
+ Endocrine System Diseases
+ Metabolic Diseases
Treatment Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
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.9 intervention groups are designated in this study
11.111% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalGroup IV
ExperimentalGroup 5
ExperimentalGroup 6
ExperimentalGroup 7
ExperimentalGroup 8
Active ComparatorGroup 9
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives