The new dosing option of ZOLADEX is aimed at pre and perimenopausal women with an increased recurrence or advanced breast cancer risk. Credit: Gorodenkoff / Shutterstock.com.
The approval of the 10.8mg dosage is supported by multiple international studies that assessed the efficacy and safety of goserelin for ovarian function suppression in premenopausal patients with HR+ breast cancerHR+ breast cancer.
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ZOLADEX is an injectable luteinising hormone-releasing hormone agonist (LHRHa) currently available in 125 countries.
It was first approved in Canada in 1989 and comes as a 3.6mg implant for 28-day dosing or as a 10.8mg implant for dosing every 12 weeks.
TerSera chief medical officer Nancy Martin stated: “TerSera is committed to supporting the unique needs of young women with HR+ breast cancerHR+ breast cancer.
“We are proud to bring this new three-month breast cancer dosing option for ZOLADEX to Canada.”
In February 2017, TerSera signed an agreement with AstraZeneca to obtain the commercial rights to Zoladex in the US and Canada.