MedPath

Relugolix

Generic Name
Relugolix
Brand Names
Myfembree, Orgovyx, Ryeqo
Drug Type
Small Molecule
Chemical Formula
C29H27F2N7O5S
CAS Number
737789-87-6
Unique Ingredient Identifier
P76B05O5V6

Overview

Relugolix is a gonadotropin-releasing hormone (GnRH) receptor antagonist used in the treatment of several hormone-responsive conditions. It was first approved in Japan in 2019, under the brand name Relumina, for the symptomatic treatment of uterine fibroids, and more recently by the United States' FDA in 2020, under the brand name Orgovyx, for the treatment of advanced prostate cancer. This branded product was later approved by the European Commission on April 29, 2022. Relugolix has also been studied in the symptomatic treatment of endometriosis. Relugolix is the first (and currently only) orally-administered GnRH receptor antagonist approved for the treatment of prostate cancer - similar therapies such as degarelix require subcutaneous administration - and therefore provides a less burdensome therapeutic option for patients who might otherwise require clinic visits for administration by healthcare professionals. In addition to its relative ease-of-use, relugolix was shown to be superior in the depression of testosterone levels when compared to leuprolide, another androgen deprivation therapy used in the treatment of prostate cancer. In May 2021, the FDA approved the combination product made up of relugolix, estradiol, and norethindrone under the market name Myfembree for the first once-daily treatment for the management of heavy menstrual bleeding associated with uterine fibroids in premenopausal women.

Indication

适用于治疗成年晚期前列腺癌症患者。

Associated Conditions

  • Advanced Hormone Sensitive Prostate Cancer
  • Advanced Prostate Cancer
  • Heavy Menstrual Bleeding
  • Severe Pain

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/06/17
Phase 2
Not yet recruiting
2024/11/04
Phase 3
Not yet recruiting
2024/10/21
Phase 3
Recruiting
2024/10/08
Phase 1
Recruiting
2024/07/15
Phase 2
Recruiting
2024/06/17
N/A
Completed
2024/06/17
Phase 2
Active, not recruiting
Atish Choudhury, MD
2024/04/23
Phase 2
Recruiting
2024/03/26
Phase 2
Not yet recruiting
2024/03/15
Phase 1
Not yet recruiting

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Sumitomo Pharma America, Inc
72974-120
ORAL
120 mg in 1 1
1/18/2024
Sumitomo Pharma America, Inc
72974-415
ORAL
40 mg in 1 1
1/18/2024

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
RYEQO 40/1/0.5 relugolix 40 mg/estradiol 1 mg/norethisterone acetate 0.5 mg film coated tablet bottle
375414
Medicine
A
9/6/2022

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