Clinical Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LEZ763



Status:Completed
Conditions:Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 65
Updated:11/23/2013
Start Date:January 2012
End Date:August 2013
Contact:Novartis Pharmaceuticals
Phone:1-888-669-6682

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A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LEZ763 Following Single and Multiple Ascending Doses in Healthy Subjects and Patients With Type 2 Diabetes


This study is a three part study to assess the safety and efficacy of LEZ763 on normal
healthy volunteers and patients with Type 2 Diabetes.


Inclusion criteria:

- All subjects: (suggest this will reduce duplication)

- Male or female aged 18-65 yr,

- Subjects must weigh at least 50 kg to participate in the study. Body mass index (BMI)
must be within the range of 18-37 kg/m2 (inclusive

- Only postmenopausal females or female subjects who report surgical sterilization
(women without child bearing potential) will be allowed in this study.

- Subjects with stable conventional sleep-wake cycle

Normal Healthy Volunteers

- Healthy male or female subjects,

- must be in good health (as determined by past medical history, physical examination,
vital signs, electrocardiogram, and laboratory tests at Screening).

Type II Diabetic Patients

- Type 2 diabetes diagnosed by American Diabetes Association criteria for at least 3
months prior to screening.

- Patients either drug naïve or on stable dose of metformin (stable dose for at least 4
weeks prior to Screening). The metformin dose should remain constant during the
course of the study.

- HbA1c 6.5 to 9.5 % inclusive at screening

Exclusion criteria:

All subjects:

- Smokers (use of tobacco products in the previous 3 months).

- Donation or loss of 400 mL or more of blood within 8 weeks prior to first dosing, or
longer if required by local regulation.

- Significant illness within two weeks prior to dosing.

- Have (or have history of) drug or alcohol abuse within the 12 months prior to dosing
or evidence of such abuse as indicated by the laboratory assays conducted during the
screening or baseline evaluations

Normal Healthy Volunteers

• History of diabetes, or adrenal disorders.

Type II Diabetic Patients

- Type 1 diabetes mellitus; positive anti-GAD antibodies; acquired or secondary forms
of diabetes such as those resulting from pancreatic surgery/injury, cystic fibrosis
related diabetes

- Evidence of clinically significant diabetic complications (such nephropathy,
retinopathy, neuropathy) Other protocol defined inclusion/exclusion criteria may
apply
We found this trial at
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Los Angeles, California 90095
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Dallas, Texas 75216
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Knoxville, Tennessee 37934
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Miami, Florida 33136
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