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Completed

NCT Number: NCT04648969

Prolonged Pulsatile Kisspeptin Administration in Hypogonadotropic Hypogonadism

The goal of this study is to develop novel treatments for patients with a condition called hypogonadotropic hypogonadism (HH) through the use of exogenous kisspeptin.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

  • Assignment: Each study subject will serve as their own control. The order of kisspeptin doses will be randomized within each set/exposure.
  • Delivery of Interventions:
  • Prior to the study visit, subjects will undergo a review of their medical history and screening laboratories. Subjects will also wear a gonadotropin releasing hormone (GnRH) pump prior to the inpatient study visit.
  • On the day of the inpatient study, the subjects will
  • Undergo q10 min blood sampling for 6 hours,
  • Receive kisspeptin intravenous (IV) boluses from hour 6 to hour 44 (20 boluses total),
  • Undergo q10 min blood samplings for another 6 hours,
  • Receive a single GnRH IV bolus at hour 51.

Who can participate

Healthy volunteers accepted: No

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

Inclusion/exclusion criteria:

  • Age 18 years and older,
  • Confirmed diagnosis of HH with
  • Low testosterone or estradiol,
  • Low or low-normal gonadotropin levels,
  • Thyroid stimulating hormone (TSH) and prolactin within the reference range,
  • Absence of abnormal pituitary or hypothalamic findings on Magnetic resonance imaging (MRI),
  • All other medical conditions stable and well controlled,
  • No prescription medications known to affect reproductive endocrine function for at least 2 months or for 5 half-lives of the drug (whichever is shorter) except for medications used to treat the subject's reproductive condition,
  • No history of a medication reaction requiring emergency medical care,
  • No illicit drug use,
  • No excessive alcohol consumption (<10 drinks/week),
  • Normal blood pressure (BP), (systolic BP < 140 mm Hg, diastolic < 90 mm Hg),
  • White blood cell, platelet counts, and TSH between 90% of the lower limit and 110% of the upper limit of the reference range,
  • Prolactin below 110% of the upper limit of the reference range,
  • Hemoglobin
  • Women: no less than 0.5 gm/dL below the lower limit of the reference range for normal women,
  • Men: on adequate testosterone replacement therapy: normal male reference range,
  • Blood urea nitrogen (BUN), creatinine, aspartate aminotransferase (AST), alanine transaminase (ALT) not elevated,
  • For women,
  • Negative serum human chorionic gonadotropin (hCG) pregnancy test at the time of screening (additional urine pregnancy test will be conducted prior to drug administration),
  • Not breastfeeding and not pregnant.

Treatment and study plan

Kisspeptin 112-121

Drug

20 intravenous doses of kisspeptin 112-121 (4 different doses of kisspeptin (randomized) in 5 sets)

Other names: metastin 45-54

GnRH

Drug

1 intravenous dose of GnRH

Other names: gonadotropin-releasing hormone

Primary outcomes

  1. Average change in luteinizing hormone (LH) pulse amplitude in response to kisspeptin

    Time frame: 52 hours

    Change in LH amplitude before, during and after kisspeptin administration

Secondary outcomes

  1. Average change in LH pulse frequency in response to kisspeptin

    Time frame: 52 hours

    Change in LH frequency before and after kisspeptin administration

Sponsors and collaborators

Lead sponsor

Stephanie B. Seminara, MD

Other

Registry information

Important dates

Study start
2019
Primary completion
2025
Study completion
2025
First posted
Dec 2, 2020
Registry last updated
Feb 18, 2026

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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