MedPath

Nateglinide

Generic Name
Nateglinide
Drug Type
Small Molecule
Chemical Formula
C19H27NO3
CAS Number
105816-04-4
Unique Ingredient Identifier
41X3PWK4O2
Background

Nateglinide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the meglitinide class of short-acting insulin secretagogues, which act by binding to β cells of the pancreas to stimulate insulin release. Nateglinide is an amino acid derivative that induces an early insulin response to meals decreasing postprandial blood glucose levels. It should only be taken with meals and meal-time doses should be skipped with any skipped meal. Approximately one month of therapy is required before a decrease in fasting blood glucose is seen. Meglitnides may have a neutral effect on weight or cause a slight increase in weight. The average weight gain caused by meglitinides appears to be lower than that caused by sulfonylureas and insulin and appears to occur only in those naïve to oral antidiabetic agents. Due to their mechanism of action, meglitinides may cause hypoglycemia although the risk is thought to be lower than that of sulfonylureas since their action is dependent on the presence of glucose. In addition to reducing postprandial and fasting blood glucose, meglitnides have been shown to decrease glycosylated hemoglobin (HbA1c) levels, which are reflective of the last 8-10 weeks of glucose control. Meglitinides appear to be more effective at lowering postprandial blood glucose than metformin, sulfonylureas and thiazolidinediones. Nateglinide is extensively metabolized in the liver and excreted in urine (83%) and feces (10%). The major metabolites possess less activity than the parent compound. One minor metabolite, the isoprene, has the same potency as its parent compound.

Indication

For the treatment of non-insulin dependent-diabetes mellitus in conjunction with diet and exercise.

Associated Conditions
Type 2 Diabetes Mellitus

A Open-label, Single-dose, 2-Sequence, 2-Period, Crossover Study to Assess Safety and Pharmacokinetics of a Nateglinide/Metformin HCl Combined Tablet Compared With a Nateglinide 120 mg Tablet and Metformin HCl 500 mg Tablet Under Fasting Conditions in Healthy Male Subjects

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
Drug: Nateglinide/Metformin
First Posted Date
2014-03-17
Last Posted Date
2014-03-17
Lead Sponsor
IlDong Pharmaceutical Co Ltd
Target Recruit Count
40
Registration Number
NCT02088918
Locations
🇰🇷

Chungnam University Hospital, Daejeon, Korea, Republic of

A Study to Assess Safety and Efficacy of ASP1941 in Combination With Nateglinide in Type 2 Diabetic Patients

Phase 3
Completed
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2011-03-16
Last Posted Date
2024-11-11
Lead Sponsor
Astellas Pharma Inc
Target Recruit Count
122
Registration Number
NCT01316107

Bioequivalence Study of Nateglinide Tablets 120 mg of Dr. Reddy's Laboratories Limited Under Fed Condition

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2010-07-12
Last Posted Date
2010-07-13
Lead Sponsor
Dr. Reddy's Laboratories Limited
Target Recruit Count
58
Registration Number
NCT01160029

Bioequivalence Study of Nateglinide Tablets 120 mg of Dr. Reddy's Laboratories Limited Under Fasting Condition

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2010-07-09
Last Posted Date
2010-07-13
Lead Sponsor
Dr. Reddy's Laboratories Limited
Target Recruit Count
68
Registration Number
NCT01159158

Effects of Nateglinide on Postprandial Glucose Excursion by Restoring Early Phase Insulin Secretion

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2009-12-14
Last Posted Date
2012-10-19
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
103
Registration Number
NCT01030952
Locations
🇨🇳

Shanghai Sixth People's Hospital, 600 Xuanshan Road, Shanghai, China

🇨🇳

Sir Run Run Shaw Hospital, 3 East Qingchun Road, Hangzhou, China

🇨🇳

Shanghai Tongji Hospital, 389 Xinchun Road, Shanghai, China

Effects of Nateglinide vs Acarbose on Postprandial Glucose Fluctuation, Dyslipidemia, and Inflammatory Factors

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2009-06-26
Last Posted Date
2012-05-10
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
160
Registration Number
NCT00928889
Locations
🇨🇳

Nanfang Hospital, the Affiliated South Hospital of the Southern Medical University, Guangzhou, China

🇨🇳

Peiking University First Hospital, BeiJing, China

🇨🇳

People's Liberation Army. The Military General Hospital of BeiJing, BeiJing, China

and more 3 locations

Study of the Durability of Glycemic Control With Nateglinide

Phase 4
Completed
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2009-03-09
Last Posted Date
2017-05-16
Lead Sponsor
Ajou University School of Medicine
Target Recruit Count
88
Registration Number
NCT00858013
Locations
🇰🇷

Korea University Guro Hospital, Seoul, Korea, Republic of

🇰🇷

Kyung hee University Medical Center, Seoul, Korea, Republic of

🇰🇷

Hanyang University Medical Center, Guri-si, Kyunggi-do, Korea, Republic of

and more 4 locations

The Effects of Nateglinide and Acarbose on the Post-Prandial Glucose Control in Type 2 Diabetic Patients

Phase 4
Completed
Conditions
Diabetes Mellitus
Type 2 Diabetes Mellitus
First Posted Date
2007-02-21
Last Posted Date
2008-03-24
Lead Sponsor
Inje University
Target Recruit Count
85
Registration Number
NCT00437918
Locations
🇰🇷

Paik Diabetes Center, Pusan Paik Hospital, College of Medicine, Inje University, Busan, Korea, Republic of

🇰🇷

Endocrinology and Metabolism, Maryknoll General Hospital, Busan, Korea, Republic of

Safety and Efficacy of Nateglinide in Patients With Type 2 Diabetes Already Taking Insulin Glargine, Metformin and/or Pioglitazone or Rosiglitazone

Phase 4
Completed
Conditions
Type 2 Diabetes
First Posted Date
2006-11-22
Last Posted Date
2017-02-24
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
28
Registration Number
NCT00402909
Locations
🇺🇸

Novartis Pharmaceuticals, East Hanover, New Jersey, United States

Efficacy and Safety of Nateglinide Treatment in Renal Transplant Recipients

Phase 4
Completed
Conditions
Renal Transplant Recipients
Posttransplant Diabetes Mellitus
Posttransplant Impaired Glucose Tolerance
First Posted Date
2006-04-27
Last Posted Date
2006-05-10
Lead Sponsor
University of Oslo School of Pharmacy
Target Recruit Count
15
Registration Number
NCT00319189
Locations
🇳🇴

Rikshospitalet, Section of Nephrology, Oslo, Norway

© Copyright 2025. All Rights Reserved by MedPath