ADT in complex patient profiles

Dr. Alberto Briganti
Full Professor of Urology
San Raffaele Hospital, Milan, Italy

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This promotional video has been sponsored by Accord Healthcare, and is intended for an international audience of healthcare professionals (HCPs).
The products mentioned may not be registered in all countries. Prescribing information may vary per country. HCPs must refer to their country prescribing information.

Orgovyx and Camcevi have extended indications in the UK:
Orgovyx(relugolix) UK prescribing information can be found here.
Camcevi (leuprolide) UK prescribing information can be found here.
Degarelix UK SmPC with legal classification and price can be found here

Orgovyx (relugolix) EU SmPC with legal classification can be found here.
Camcevi (leuprolide) EU SmPC with legal classification can be found here.
Degarelix EU SmPC with legal classification can be found here

Orgovyx EU indication: Orgovyx is indicated for the treatment of adult patients with advanced metastatic hormone-sensitive prostate cancer.
Cardiovascular disease such as myocardial infarction and stroke has been reported in the medical literature in patients with androgen deprivation therapy. Therefore, all cardiovascular risk factors should be taken into account. 
The most commonly observed adverse reactions during relugolix therapy are physiological effects of testosterone suppression, including hot flushes (54%), musculoskeletal pain (30%), and fatigue (26%). Other very common adverse reactions include diarrhoea and constipation (12% each).

This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

 Adverse events should be reported. For UK healthcare professionals, reporting forms, and information can be found at https://yellowcard.mhra.gov.uk/Adverse events should also be reported to Accord-UK LTD on 01271 385257 or email  medinfo@accord-healthcare.com. For non-UK/EU healthcare professionals, you can report side effects directly via the national reporting system listed in Appendix V of the EU SmPC.

This educational activity is sponsored by

EUR-Onc-Org-01715 – June 2026

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