Effects of Leptin Treatment on Weight Loss

Leptin Treatment for Prevention of the Metabolic and Endocrine Sequelae of a Decreased Caloric Intake: Studies of Patients on a Very Low Calorie Diet

This is a double blind placebo controlled clinical study designed to determine the effects of leptin on the changes that occur in the body during weight loss achieved by a very low calorie diet.

Study Overview

• Status: Completed
• Conditions: Obesity
• Intervention / Treatment: Drug: Leptin; Behavioral: Very Low Calorie Diet

Detailed Description

Leptin is a hormone that is produced by the fat tissue and acts on the brain. Leptin plays a key role in regulating energy balance and body weight in animals and in humans.

When a person loses weight, leptin concentration in the blood is reduced. Reduction in blood leptin levels has been found to be related to a decreased metabolic rate (the rate in which the body burns its calories), an increased appetite, and to many other physiological and hormonal changes that may lead to failure in dieting.

This study is aimed to test if maintaining leptin in the pre-diet level range will ameliorate the changes that occur in the body during weight loss. If these changes are reduced, the process of weight loss could be easier and faster when adhering to a low calorie diet.

In this study, leptin or placebo is administered by an injection under the skin, in a way that is similar to injections of insulin to diabetic patients. 50% of the subjects participating in the study are treated by leptin and 50% are treated by placebo. Blood leptin levels are maintained in the pre-diet range in leptin treated subjects by leptin treatment. Subjects treated by placebo will also lose weight if they adhere to the liquid diet provided by the Rockefeller University Bio-nutrition Department. The investigators and the participants don't know if leptin or placebo are used since this is a double blind study.

To participate in this study, subjects have to stay at the Rockefeller University Hospital as inpatients for about two months and continue the study as outpatients for 4 more months. During the outpatient period, subjects have to attend a clinic visit once a week. During the first 3 weeks of the study, subjects are introduced to a weight stabilization liquid diet. During this time, the initial weight is maintained and baseline study tests are performed. When testing is completed, a very low calorie liquid diet and leptin or placebo administration are initiated. Weight is monitored until 10% weight loss is achieved. At this time, a second testing period is performed in an inpatient setting. When testing is completed, weight loss and leptin or placebo treatment continue at home in an outpatient setting until 20% weight loss is achieved. When this period is completed, a third testing period is performed in an inpatient setting. The last month of the study is dedicated to a transition from the liquid diet to solid food, and to weight maintenance education provided by the hospital staff in an outpatient setting. A solid food weight maintenance diet is provided to participants during this period. At the end of this period, two days of testing are performed and leptin/placebo administration is discontinued.

Study testing periods are performed over 12 days in an inpatient setting and include a variety of blood draws, urine collection, and metabolic and behavioral tests that are known to be affected by weight loss.

• Study Type: Interventional
• Enrollment (Anticipated): 40
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • New York
    • New York, New York, United States, 10065
      • Rockefeller University Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 45 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

(1) adult females, age 25-45 with BMI 29-45, and no other acute or chronic illnesses. Pregnant women will not be permitted to participate in the study.

Exclusion Criteria:

1. Chronic illnesses other the than mild forms illnesses related to obesity (hypertension, hyperlipidemia etc) that do not require medical treatment
2. Diabetes Mellitus
3. Chronic drug treatment for any medical conditions
4. Inability to give informed consent
5. Inability to give contact information (for outpatient follow up) including permanent residence, provide evidence of a stable living environment for the study period.
6. Active weight reduction of more than 7 pounds in the last 3 months
7. Weight at screening more than 6% lower than the maximal life time weight.
8. History of bleeding or blood clotting disorders.
9. Changes in smoking habits for the last 3 months.
10. Pregnancy or breast feeding in women.
11. Allergic reaction to local anesthetics
12. History of anaphylaxis or anaphylactoid-like reactions
13. Tendency to form scars (keloids) easily
14. Subjects with known hypersensitivity to E Coli-derived proteins or any other component of the A-100 preparation.
15. Irregular menses
16. HIV and hepatitis B or C positive subjects.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: VLCD and leptin; Very low calorie diet formula providing 800 calories per day and leptin treatment.	Drug: Leptin; Leptin is an adipocyte hormone that functions as an afferent signal in a feedback loop regulating body weight; Other Names: A-100; Recombinant-methionyl Human Leptin (r-metHuLeptin)
Active Comparator: placebo; Very low calorie diet and placebo treatment	Behavioral: Very Low Calorie Diet; placebo injections

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
energy expenditure after 10% and 20% weight loss, achieved by a VLCD with or without A-100 treatment	Testing period 2,3 and 4 after 10% and 20% weight loss

Secondary Outcome Measures

Outcome Measure	Time Frame
endocrine and behavioral parameters	testing period 2, 3 and 4. After 10% and 20% weight loss

Collaborators and Investigators

• Sponsor: Rockefeller University
• Collaborators: Columbia University; Weill Medical College of Cornell University; St. Luke's-Roosevelt Hospital Center
• Investigators: Principal Investigator: Jeffrey Friedman, MD, PHD, Rockefeller University

Study record dates

Study Major Dates

• Study Start: March 1, 2001
• Primary Completion (Actual): November 1, 2006
• Study Completion (Actual): June 1, 2009

Study Registration Dates

• First Submitted: December 19, 2002
• First Submitted That Met QC Criteria: December 20, 2002
• First Posted (Estimate): December 23, 2002

Study Record Updates

• Last Update Posted (Estimate): October 19, 2010
• Last Update Submitted That Met QC Criteria: October 18, 2010
• Last Verified: October 1, 2010

More Information

Terms related to this study

• Keywords: Obesity; Overweight; Diet; Fat; Leptin; Weightloss; Reducing
• Additional Relevant MeSH Terms: Overnutrition; Nutrition Disorders; Overweight; Body Weight; Obesity
• Other Study ID Numbers: JFN 0357

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No