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Completed

NCT Number: NCT00474279

Effects of an Oral GH Secretagogue (MK-677) on Body Composition and Functional Ability of Older Adults

The purpose of this study is to determine whether treatment of healthy older men and women with oral MK-677 for 12 months will enhance pulsatile GH release and increase mean GH and IGF-I concentrations into the range of young adults and will have favorable effects on body composition and functional ability on older adults.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of Virginia

Charlottesville, Virginia, 22908, United States

About this study

This is a two year, double-blind, placebo-controlled cross-over trial of once daily administration of MK-677, an oral GH secretagogue, to healthy older adults. During the first year, subjects will be randomized to MK-677 or placebo treatment. In each of three subgroups of subjects (men, women off and women on hormone replacement therapy), 16 subjects will receive MK-677 and 8 will receive placebo. After 1 year, the subjects who received placebo will be switched to MK-677 treatment; the subjects who received MK-677 for the first year will be randomized to either placebo or MK-677 for the second year of the study.The study will test changes in GH, IGF-I, body composition and function.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men and women  60 years of age, with a body mass index of < 35 kg/m2.

Exclusion criteria

  • Medication known to affect GH secretion, other than estrogen replacement therapy
  • Coronary artery disease,
  • Congestive heart failure,
  • Peripheral vascular disease,
  • Diabetes mellitus (requiring insulin or an oral hypoglycemic agent),
  • Significant hypertension (BP >180 systolic or >100 diastolic at rest);
  • Renal, hepatic, pulmonary disease;
  • Untreated hypothyroidism, untreated hyperthyroidism;
  • History of seizure disorder;
  • History of malignancy (other than some skin cancers), history of active chronic infections (e.g., HIV, tuberculosis).
  • Hematocrit < 40%, men, < 36%, women
  • History of daily tobacco use within past 3 months
  • Chronic alcohol abuse
  • Strenuous exercise for average of more than 60 min/day
  • Investigational drug within past 6 weeks
  • Psychiatric history, especially anorexia nervosa
  • Transmeridian travel within 2 weeks prior to or during study

Treatment and study plan

Orally active growth hormone secretagogue (MK-677)

Drug

Primary outcomes

  1. At 12 months: 24-hour mean growth hormone concentrations

  2. Insulin-like growth factor-I concentrations

  3. Body weight and fat mass, specifically abdominal visceral fat

  4. Fat-free mass

  5. Safety determined by routine laboratory tests at 1 to 3 month intervals, yearly pap smears and mammograms

Secondary outcomes

  1. at 12 months: Growth hormone secretory dynamics

  2. Isokinetic muscle strength (knee and shoulder)

  3. Thigh muscle cross-sectional area

  4. Function tests (timed walks, stair climb, chair rise)

  5. Quality of life assessments

  6. Insulin sensitivity

  7. Lipid profile

  8. Resting metabolic rate

  9. Aerobic exercise capacity

  10. Exploratory outcomes:

  11. effects of gender and HRT on primary outcomes

  12. effects of treatment in year 2: Year 2 outcomes include effects of continuation on MK-677, or crossover to placebo, placebo to MK-677

  13. bone mineral density at end of year 2.

Sponsors and collaborators

Lead sponsor

University of Virginia

Other

Registry information

Acronym: MOT089

Important dates

Study start
1998
Study completion
2004
First posted
May 16, 2007
Registry last updated
May 16, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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