Dose-finding Study of LIK066 Compared With Placebo or Sitagliptin to Evaluate Change in HbA1c in Patients With Diabetes



Status:Completed
Conditions:Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:21 - 65
Updated:5/3/2014
Start Date:December 2013
End Date:April 2014
Contact:Novartis Pharmaceuticals
Phone:1-888-669-6682

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A Multi-center, Randomized, Double-blind, Parallel-group Dose-finding Study to Evaluate Change in HbA1c After 12 Weeks With 7 Doses of LIK066 Compared With Placebo or Sitagliptin in Patients With Type 2 Diabetes

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


Inclusion Criteria:

1. Confirmed diagnosis of T2DM by standard criteria

2. Drug-naïve patients, defined as patients not having received any anti-diabetic
medication previously,

3. 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

4. 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)

5. HbA1c ≥ 7 to ≤ 10.5% at Visit 1 for drug-naïve/currently untreated patients

6. HbA1c ≥ 7 to ≤ 9.5% at Visit 1 for patients treated with OAD monotherapy

7. HbA1c ≥ 7 to ≤ 10.5% at Visit 199 for ALL patients

8. Age: ≥18 and ≤ 75 years old at Visit 1

9. BMI ≥22 to ≤45 kg/m2 at Visit 1

Exclusion Criteria:

1. 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

2. 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

3. History of acute metabolic complications, CV disease, type 1 diabetes mellitus,
hepatic disorders, pancreatitis, chronic diarrhea

4. 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

5. ECG abnormalities including AV block, long QT syndrome or QTc>450 msec for men and
>470 msec for women

6. History of malignancy

7. Women of child-bearing potential not using effective methods of contraception Other
protocol-defined inclusion/exclusion criteria may apply
We found this trial at
9
sites
Greensboro, North Carolina 27401
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Greensboro, NC
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Arlington, Virginia 22203
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Arlington, VA
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Charleston, South Carolina 29407
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Charleston, SC
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Edina, Minnesota 55435
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Edina, MN
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Feasterville Trevose, Pennsylvania 19053
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Feasterville Trevose, PA
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Hawaiian Gardens, California 90716
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Hawaiian Gardens, CA
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Salisbury, North Carolina 28144
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Salisbury, NC
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St. Louis, Missouri 63110
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St. Louis, MO
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Winston-Salem, North Carolina 27157
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Winston-Salem, NC
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