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Hormone Therapy

Kisspeptin for Reproductive Disorders

Phase 1
Waitlist Available
Led By Stephanie B. Seminara, MD
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Healthy men between 21 and 40 years old with normal erectile and ejaculatory function, and testicular volume >15 ml
Men and women with hypogonadotropic hypogonadism
Must not have
Subjects with reproductive disorders with history of a medication reaction requiring emergency medical care, and those with pituitary adenoma or a macroprolactinoma confirmed on MRI imaging
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to understand how kisspeptin, a hormone that triggers the release of another hormone, affects people with certain reproductive disorders. Participants with specific reproductive health issues will receive kisspeptin to see if their bodies can respond correctly. The goal is to learn more about reproductive health and improve future diagnostics.

Who is the study for?
This trial is for healthy men (21-40) with normal sexual function, women (21-40) with regular menstrual cycles, postmenopausal women (50-60), and individuals diagnosed with reproductive disorders like PCOS or hypogonadotropic hypogonadism. Participants should not have chronic diseases, a history of severe medication reactions, or excessive substance use.
What is being tested?
The study investigates the effects of kisspeptin on the reproductive system by administering it to participants. Kisspeptin is known to trigger hormone release including GnRH which plays a key role in reproduction.
What are the potential side effects?
Potential side effects are not explicitly listed but may include reactions related to hormonal changes such as mood swings, acne, weight change, or injection site discomfort.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am a healthy man, 21-40, with normal sexual and testicular function.
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I have been diagnosed with hypogonadotropic hypogonadism.
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I am a healthy woman who has gone through menopause.
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I do not use illegal drugs and drink less than 10 alcoholic drinks a week.
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I have normal sexual function and no reproductive health issues.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I have a reproductive disorder and have had a severe medication reaction or a confirmed pituitary tumor.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Side effects data

From 2009 Phase 2 trial • 36 Patients • NCT00586898
22%
Hyperglycemia
19%
Hot Flashes
17%
Dyspnea
14%
Hyperkalemia
8%
SGPT (ALT)
6%
Hypoglycemia
3%
Pneumonitis
3%
Cardiovascular, other
100%
80%
60%
40%
20%
0%
Study treatment Arm
All Participants

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: kisspeptin, GnRHExperimental Treatment2 Interventions
Intravenous (IV) or subcutaneous (SC) administration of kisspeptin 112-121 and/or administration of GnRH
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
kisspeptin 112-121
2013
Completed Phase 1
~420
GnRH
2017
Completed Phase 2
~640

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Hypogonadotropic Hypogonadism (HH) include the administration of gonadotropin-releasing hormone (GnRH) and its analogs, as well as kisspeptin. GnRH therapy works by stimulating the pituitary gland to release luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which are crucial for gonadal function and sexual development. Kisspeptin, a naturally occurring hormone, also stimulates the release of GnRH, thereby promoting the secretion of LH and FSH. These treatments are vital for HH patients as they help restore normal reproductive function and hormonal balance, addressing symptoms such as delayed puberty and infertility.
[Pulsatile administration of GnRH: from the future to the present].Diurnal modulation of rat hypothalamic gonadotropin-releasing hormone release by melatonin in vitro.Kisspeptin modulates sexual and emotional brain processing in humans.

Find a Location

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

Massachusetts General HospitalLead Sponsor
3,006 Previous Clinical Trials
13,307,026 Total Patients Enrolled
Stephanie B. Seminara, MD3.73 ReviewsPrincipal Investigator - Massachusetts General Hospital
Massachusetts General Hospital
5Patient Review
This doctor is very caring and thinks critically about symptoms. They help uplift patients' spirits and have amazing bedside manner!
Stephanie B Seminara, MDPrincipal InvestigatorMassachusetts General Hospital
8 Previous Clinical Trials
4,917 Total Patients Enrolled

Media Library

GnRH (Hormone Therapy) Clinical Trial Eligibility Overview. Trial Name: NCT00914823 — Phase 1
Hypogonadotropic Hypogonadism Research Study Groups: kisspeptin, GnRH
Hypogonadotropic Hypogonadism Clinical Trial 2023: GnRH Highlights & Side Effects. Trial Name: NCT00914823 — Phase 1
GnRH (Hormone Therapy) 2023 Treatment Timeline for Medical Study. Trial Name: NCT00914823 — Phase 1
~16 spots leftby Nov 2025