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For adult patients with non-metastatic castration-resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease

Patient Image - Nubeqa

Introducing NUBEQA:

Significantly delays metastasis with Androgen Deprivation Therapy vs. Androgen Deprivation Therapy alone, without increasing the rate of treatment discontinuation due to adverse events.

For men with nmCRPC who are at high risk of developing metastatic disease, progression to mCRPC is a tipping point for increased sufering and mortality. NUBEQA is a novel androgen receptor inhibitor for nmCRPC that extends median metastasis-free survival (MFS) without increasing the rate of treatment discontinuation due to adverse events vs. ADT alone.

The benefits of NUBEQA have been demonstrated in the ARAMIS study, the largest phase 3 study of nmCRPC to date (N=1,509).

Patient Image - Nubeqa

NUBEQA® is indicated for the treatment of adult men

with non-metastatic castration-resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease

Do current therapies help you achieve the treatment goals of men with nmCRPC?

Delay metastasis

NUBEQA + ADT delivers:​

40.4 months MFS - more than double the median MFS of ADT

Maintain your patient’s current lifestyle

NUBEQA + ADT delivers:​

Discontinuation rate comparable​
to ADT

Patient Image - Nubeqa

Add NUBEQA to ADT to significantly delay metastasis and improve overall survival vs. ADT alone,

without increasing the rate of treatment discontinuation due to adverse events

NUBEQA® (darolutamide) | Metastasis Free Survival
Explore NUBEQA and its impact on metastasis-free survival in nmCRPC.
PP-NUB-IE-0265-1, December 2025
NUBEQA® (darolutamide) | Overall Survival​
Explore NUBEQA and its impact on overall survival.
PP-NUB-IE-0266-1, December 2025
NUBEQA® (darolutamide) | Morbidity
Explore NUBEQA® and its secondary endpoints.
PP-NUB-IE-0267-1, December 2025

PP-NUB-IE-0264-1   |   December 2025


    Referencesexpand_less
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      NUBEQA® (darolutamide) Summary of Product Characteristics.
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      Fizazi K et al. N Engl J Med. 2019;380(13):1235–1246.
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