ORGOVYX HCP Website | ORGOVYX.ca

ORGOVYX® (relugolix tablets, 120 mg) is indicated for the treatment of adult patients with advanced prostate cancer.²

EFFICACY PROFILE

Evaluate the ORGOVYX® efficacy data from the HERO study:

Testosterone suppression
data (Day 29 to Week 48)

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Testosterone suppression
data at Day 15Learn More

Testosterone
recovery dataLearn More

SAFETY PROFILE

Evaluate the safety profile from the HERO study.

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DOSING AND
ADMINISTRATION

Find dosing and administration information related to ORGOVYX®.

About ORGOVYX®

HERO STUDY

Learn more about the HERO study, which evaluated ORGOVYX® in advanced prostate cancer patients.

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Resources

Access relevant information and additional resources for you and your patients.

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Click here for additional safety information and for a link to the Product Monograph for more information about:

The most serious warnings and precautions regarding QT prolongation.
Relevant warnings and precautions regarding co-administration with an oral P-gp inhibitor or combined P-gp and strong cytochrome P450 (CYP) 3A inducer, advising patients that ADT can prolong the QT interval, tests of pituitary gonadotropic and gonadal functions, monitoring PSA levels, periodic monitoring in those at risk of QTc prolongation and electrolyte abnormality, risk of decreased bone density, use of contraceptives, and fertility in males of reproductive potential.
Conditions of clinical use, adverse reactions, drug interactions, and dosing instructions not discussed elsewhere in the piece.

The Product Monograph is also available by calling 1-866-260-6291.

ADT: androgen deprivation therapy; P-gp: P-glycoprotein; PSA: prostate-specific antigen
^*Comparative clinical significance has not been established.

References: 1. Data on file - First and only. Sumitomo Pharma Canada, Inc. December 6, 2023. 2. ORGOVYX® Product Monograph. Sumitomo Pharma Switzerland GmbH. November 3, 2023.

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