A Phase 2 Study to Evaluate the Effects of ASP5541 in Participants With Prostate Cancer
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
Hormone therapy, or androgen deprivation therapy (ADT) is a standard way to treat prostate cancer. It works by reducing the amount of the main male sex hormone, testosterone in the body. Androgen receptor pathway inhibitors (ARPIs) are another type of hormone therapy. They either slow down how much testosterone is made or block testosterone from reaching the prostate cancer cells. Abiraterone acetate (AA) is an ARPI that is used to treat advanced prostate cancer. This type of treatment is usually given as a tablet with a steroid called prednisone/prednisolone to manage any medical problems from the hormone therapy. ASP5541 is a different form of abiraterone acetate. It is given as an injection into the muscle. In this study, ASP5541 will be given to men with advanced prostate cancer, both with and without prednisone/prednisolone. This study will check the safety of ASP5541 and compare how well ASP5541 works in men with advanced prostate cancer compared to abiraterone acetate. The main aims of the study are: * To check how well ASP5541 with prednisone/prednisolone works compared to AA with prednisone/prednisolone in men with advanced prostate cancer who haven't previously been treated with an ARPI. * To check the safety of ASP5541 given by itself in men with advanced prostate cancer that haven't previously been treated with an ARPI. * To check how well ASP5541 given by itself works compared to AA with prednisone/prednisolone in men with advanced prostate cancer that haven't previously been treated with an ARPI. * To check the safety of ASP5541 with prednisone/prednisolone in Japanese men with advanced prostate cancer. Adult men with a certain type of advanced prostate cancer can take part. Their cancer has spread to other parts of the body (metastatic). The different types are: * Metastatic hormone-sensitive prostate cancer (mHSPC). Prostate cancer that needs testosterone to grow. * Metastatic castration-resistant prostate cancer (mCRPC). Prostate cancer that continues to grow even when testosterone levels are low. In this study there will be 3 treatment groups: * In Group 1, men with mCRPC who haven't previously been treated with an androgen receptor pathway inhibitor will either be given ASP5541 and prednisone/prednisolone or be given abiraterone acetate and prednisone/prednisolone. * In Group 2, men with mHSPC who haven't previously been treated with an androgen receptor pathway inhibitor will either be given ASP5541 by itself or be given abiraterone acetate with prednisone/prednisolone. * In Group 3, Japanese men with mCRPC or mHSPC who may or may not have previously been treated with an androgen receptor pathway inhibitor will be given ASP5541 with prednisone/prednisolone. ASP5541 will be given as an injection into a muscle every 12 weeks. Men with mCRPC will take prednisone/prednisolone twice daily and men with mHSPC will take prednisone/prednisolone once daily. Abiraterone acetate will be given as tablets to be taken once daily. All groups will also receive the standard of care treatment, such as androgen deprivation therapy. The men in the study will visit their clinic regularly during and after treatment for health checks, including checking for any medical problems. Some men (Group 2) will check their blood pressure weekly at home. On some visits they will also have scans to check for any changes in their cancer. The number of visits and type of safety checks done at each visit will depend on the health of each person and when they completed their treatment.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Mężczyźni z zaawansowanym rakiem prostaty, który rozprzestrzenił się na inne części ciała.
- •Rak prostaty wymaga testosteronu do wzrostu (hormonowrażliwy) lub przestał reagować na terapię hormonalną (oporny na kastrację).
- •Rak prostaty musi być potwierdzony badaniami (np. biopsją).
- •Pacjent czuje się na tyle dobrze, by móc uczestniczyć w badaniu (nawet jeśli odczuwa ból w kościach).
- •Oczekiwana długość życia pacjenta wynosi co najmniej 12 miesięcy (dla raka hormonowrażliwego) lub 6 miesięcy (dla raka opornego na kastrację).
- •Pacjent musi być w stanie zrozumieć i przestrzegać zasad badania.
- •Pacjent jest leczony terapią hormonalną (zastrzyki lub operacja zmniejszająca poziom testosteronu) od co najmniej 14 dni przed rozpoczęciem badania (dla raka hormonowrażliwego).
✗ Disqualifies
- •Rak prostaty z pewnymi innymi cechami komórek (np. neuroendokrynne, drobnokomórkowe).
- •Pacjent z zaawansowanym rakiem prostaty, który wcześniej nie był leczony lekiem blokującym receptory androgenowe (np. abirateronem).
- •Niski poziom testosteronu we krwi (poniżej określonego progu) w przypadku raka opornego na kastrację.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- July 15, 2026
- Sex
- Male only
Therapies / drugs in trial
Locations (50)
Clearview Cancer Institute
Huntsville, United States
Sharp HealthCare - Sharp Memorial Hospital
San Diego, United States
H. Lee Moffitt Cancer Center
Tampa, United States
Associated Urological Specialists
Chicago Ridge, United States
NorthShore University HealthSystem
Evanston, United States
Ochsner Health - Ochsner Medical Center - New Orleans
New Orleans, United States
New Mexico Oncology Hematology Consultants
Albuquerque, United States
Solaris Health - The Urology Group
Cincinnati, United States
Carolina Urologic Research Center
Myrtle Beach, United States
Tennessee Oncology Nashville
Nashville, United States
University of Virginia Cancer Center
Charlottesville, United States
UW Health Carbone Cancer Center
Madison, United States
Subei People's Hospital
Yangzhou, China
The Second Hospital of Tianjin Medical University
Tianjin, China
The First Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, China
Huai'an First People's Hospital
Huaian, China
Renji Hospital Shanghai Jiaotong Univ School of Medicine
Shanghai, China
Site FR33003
Bordeaux, France
Site FR33008
Lille, France
Site FR33006
Paris, France
Site FR33004
Strasbourg, France
Site DE49004
Nürtingen, Germany
Site DE49001
Heinsberg, Germany
Site IT39004
Milan, Italy
Site IT39006
Milan, Italy
Site IT39005
Roma, Italy
Site IT39003
Trento, Italy
National Cancer Center Hospital East
Kashiwa, Japan
Shizuoka Cancer Center
Sunto-gun, Japan
Nippon Medical School Hospital
Bunkyo-ku, Japan
The Cancer Institute Hospital of JFCR
Koto, Japan
Harasanshin Hospital
Fukuoka, Japan
Osaka International Cancer Institute
Osaka, Japan
Site PL48005
Mysłowice, Poland
Site PL48008
Otwock, Poland
PanOncology Trials
San Juan, Puerto Rico
Site KR82006
Daegu, South Korea
Site KR82008
Gwangju, South Korea
Site KR82002
Seoul, South Korea
Site KR82003
Seoul, South Korea
Site KR82004
Seoul, South Korea
Site KR82007
Seoul, South Korea
Site ES34006
Barcelona, Spain
Site ES34005
Barcelona, Spain
Site ES34008
Barcelona, Spain
Site ES34001
Madrid, Spain
Site ES34003
Santiago de Compostela, Spain
Site TW88603
Kaohsiung City, Taiwan
Site TW88602
Taipei, Taiwan
Site GB44003
London, United Kingdom
Trial contact
Astellas Pharma Global Development, Inc.
Contact information from ClinicalTrials.gov. Contact in English.
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Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/8/2026.
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