ORGOVYX® WAS GENERALLY WELL TOLERATED1

ADVERSE REACTIONS (≥ 5%) OF PATIENTS WITH ADVANCED PROSTATE CANCER WHO RECEIVED ORGOVYX® IN THE HERO STUDY

Table for safety profile
Adapted from the Product Monograph.1
  • a Includes diarrhea and colitis.
  • b Includes fatigue and asthenia.
  • c Includes arthralgia, back pain, pain in extremity, musculoskeletal pain, myalgia, bone pain, neck pain, arthritis, musculoskeletal stiffness, non-cardiac chest pain,
    musculoskeletal chest pain, spinal pain, and musculoskeletal discomfort.
  • Permanent discontinuation due to an adverse reaction occurred in 3.5% of patients receiving ORGOVYX®.
  • Serious adverse reactions occurred in 12% of patients receiving ORGOVYX®.
Data

Efficacy Profile

Evaluate the ORGOVYX® efficacy data from the HERO study.

Learn More
Pill

Dosing and Administration

Find dosing and administration information related to ORGOVYX®.

Learn More

Reference: 1. ORGOVYX® Product Monograph. Sumitomo Pharma Switzerland GmbH. November 3, 2023.

Sumitomo Logo

is a trademark of Sumitomo Pharma Co., Ltd., used under license.

SUMITOMO PHARMA is a trademark of Sumitomo Pharma Co., Ltd., used under license.

SUMITOMO is a registered trademark of Sumitomo Chemical Co., Ltd., used under license.

ORGOVYX® and its associated logo are registered trademarks of Sumitomo Pharma Switzerland GmbH.

© 2024 Sumitomo Pharma Canada, Inc. All rights reserved. RGX-CA-00013-24

IMC LogoPAAB Logo