Current partner codePEPTIDESDE

Trial of Leptin Administration After Roux-en-Y Gastric Bypass

Status

Completed

Phase

Phase 1 / Phase 2

Enrollment

31

Locations

1

Results

Posted

Publications

0

Study summary

What the protocol is testing.

This is a pilot and feasibility study to examine a novel intervention using leptin in weight-reduced individuals who have undergone bariatric surgery but still remain obese. Leptin, a peptide hormone secreted from adipose tissue, is a regulator of food intake and energy expenditure. Administration of leptin resulted in profound weight reduction in the few reported cases of obese individuals with genetic leptin deficiency. However, most obese people have increased leptin levels. Such individuals are said to be in a "leptin-resistant" state, whereby administration of physiological concentrations of leptin are ineffective at producing significant weight reduction. Roux-en-Y gastric bypass surgery (RYGBP) is more effective than diet alone in producing long-term reduction of body weight. Yet even after surgery there is a plateau in weight loss though the individual may still be obese and have or be at risk for obesity related morbidities. The investigators have shown that plasma leptin levels are significantly lower in women after RYGBP compared with BMI-matched controls. This state of relative hypoleptinemia or leptin insufficiency suggests that post-RYGBP individuals may be in a "leptin-sensitive" state and, thus, would undergo further weight loss when administered doses of leptin that would not normally result in significant weight reduction. This study will examine the effects of leptin administered by self-injection twice per day on body weight and endocrine function. All individuals will received leptin and placebo and different times during the 34 week study period.

Full detailed description

Metreleptin will be self-administered by subcutaneous injection at 0.05 mg/kg body weight twice per day (i.e. at 8 am and 8 pm). This dose was chosen because it would not be expected to cause substantial weight loss in an obese non-surgical population, nor should it incur any substantial injection site reactions. Subjects will receive a demonstration of dose preparation and injection in addition to written instructions with visual aides. After the run-in period, subjects will demonstrate their preparation and injection technique. Placebo injections will consist of sterile water equal in volume to that of the metreleptin dose calculated for each individual. Subjects will be instructed to continue with their current level of physical activity. At week 16, each subject will cross-over to the alternate treatment for an additional 16 weeks.

Interventions

Treatment arms and agents.

DRUG

Leptin

Leptin self-administered subcutaneously at 0.05 mg/kg body weight twice each day

OTHER

Placebo

Sterile water equal in volume to that of the metreleptin dose calculated for each individual self-administered subcutaneously twice each day

Timeline

From registration to results.

  1. First posted

    Jul 4, 2008

  2. Study start

    Apr 2008

  3. Primary completion

    Aug 2012

  4. Study completion

    Jul 2014

  5. Results posted

    Nov 16, 2015

  6. Registry updated

    Nov 16, 2015

Outcomes

What the study measures.

Primary outcomes

Weight Change (in kg.) After Each Intervention

Time frame · 0 weeks, 16 weeks and 32 weeks

For the Leptin Intervention, 16 week values were compared to baseline for those who received Leptin in the first period, and 32 week values were compared to 16 week values in those who received Leptin in the second period. For the Placebo Intervention, 16 week values were compared to baseline for those who received Placebo in the first period, and 32 week values were compared to 16 week values in those who received Placebo in the second period.

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
25 Years
Maximum age
65 Years
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Women ages 25-65 years who are 18 months to 15 years Roux-en-Y gastric bypass * Current BMI of 28-50 kg/m2 and a percent total body weight loss from highest pre-surgical weight of \>20% and \<45% * Must live in the vicinity of New York City to comply with 11 study visits over 34 weeks * Must be willing to self-inject study drug twice per day Exclusion Criteria: * Diabetes * History of plastic surgery

Study locations

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

Columbia University Medical Center

New York, New York, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Metreleptin.

Related PeptideStat pages

Put the record in context.

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