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GnRH agonist/antagonist

Memorial Sloan Kettering Cancer Center · FDA-approved active Small molecule

GnRH agonist/antagonist is a GnRH agonist/antagonist Small molecule drug developed by Memorial Sloan Kettering Cancer Center. It is currently FDA-approved for Prostate cancer (hormone-sensitive), Breast cancer (hormone-sensitive), Cancer treatment-related hot flashes and sexual dysfunction.

GnRH agonists/antagonists suppress gonadotropin-releasing hormone signaling to reduce sex hormone production, used in oncology to manage hormone-sensitive cancers and their treatment side effects.

GnRH agonists/antagonists suppress gonadotropin-releasing hormone signaling to reduce sex hormone production, used in oncology to manage hormone-sensitive cancers and their treatment side effects. Used for Prostate cancer (hormone-sensitive), Breast cancer (hormone-sensitive), Cancer treatment-related hot flashes and sexual dysfunction.

At a glance

Generic nameGnRH agonist/antagonist
SponsorMemorial Sloan Kettering Cancer Center
Drug classGnRH agonist/antagonist
TargetGnRH receptor
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

GnRH agonists initially stimulate the pituitary gland before causing desensitization, leading to decreased luteinizing hormone and follicle-stimulating hormone, which reduces testosterone and estrogen production. GnRH antagonists directly block GnRH receptors to immediately suppress gonadotropin release. Both approaches are used in prostate cancer, breast cancer, and to mitigate hot flashes and sexual dysfunction caused by cancer therapies.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about GnRH agonist/antagonist

What is GnRH agonist/antagonist?

GnRH agonist/antagonist is a GnRH agonist/antagonist drug developed by Memorial Sloan Kettering Cancer Center, indicated for Prostate cancer (hormone-sensitive), Breast cancer (hormone-sensitive), Cancer treatment-related hot flashes and sexual dysfunction.

How does GnRH agonist/antagonist work?

GnRH agonists/antagonists suppress gonadotropin-releasing hormone signaling to reduce sex hormone production, used in oncology to manage hormone-sensitive cancers and their treatment side effects.

What is GnRH agonist/antagonist used for?

GnRH agonist/antagonist is indicated for Prostate cancer (hormone-sensitive), Breast cancer (hormone-sensitive), Cancer treatment-related hot flashes and sexual dysfunction.

Who makes GnRH agonist/antagonist?

GnRH agonist/antagonist is developed and marketed by Memorial Sloan Kettering Cancer Center (see full Memorial Sloan Kettering Cancer Center pipeline at /company/memorial-sloan-kettering-cancer-center).

What drug class is GnRH agonist/antagonist in?

GnRH agonist/antagonist belongs to the GnRH agonist/antagonist class. See all GnRH agonist/antagonist drugs at /class/gnrh-agonist-antagonist.

What development phase is GnRH agonist/antagonist in?

GnRH agonist/antagonist is FDA-approved (marketed).

What are the side effects of GnRH agonist/antagonist?

Common side effects of GnRH agonist/antagonist include Hot flashes, Sexual dysfunction, Injection site reactions, Fatigue, Bone density loss (with long-term use).

What does GnRH agonist/antagonist target?

GnRH agonist/antagonist targets GnRH receptor and is a GnRH agonist/antagonist.

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