Badanie obserwacyjne mające na celu dowiedzenie się więcej na temat bezpieczeństwa darolutamidu u mężczyzn chorych na raka prostaty w Korei
Badanie nadzoru po wprowadzeniu do obrotu dotyczące zatwierdzonego stosowania darolutamidu u pacjentów z Korei
This is an observational study in which participants receive a treatment which is already available for doctors to prescribe for non-metastatic castration-resistant prostate cancer (nmCRPC) or metastatic hormone-sensitive prostate cancer (mHSPC). nmCRPC is a prostate cancer that has not yet spread to other parts of the body and does not respond to lowering testosterone in the body. mHSPC is a prostate cancer that has spread to other parts of the body and can be treated by lowering testosterone levels.
This study looks at the safety of the study drug, darolutamide, in Korean patients with nmCRPC or mHSPC. Darolutamide is currently available for doctors to prescribe to men with nmCRPC or mHSPC. It works by attaching to the special molecules called androgen receptors (AR) within prostate cells and blocks hormones called androgens from attaching to AR, which helps delay cancer growth.
To learn more about the safety of Darolutamide, the researchers will study whether the participants have adverse events. An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events that happen in studies, even if they do not think the adverse events might be related to the study treatments. The researchers will also learn more about how well darolutamide is working in these participants.
During this study, the researchers will collect information from the medical records of patients who have been prescribed darolutamide by their doctors.
Each participant will be in this study for 1 year. The whole study will last about 6 years. During this time, the participants will visit their doctor every 2 to 4 months as part of their usual care. At these visits, the doctors will do scans to check the patients' cancer and take blood samples. The patients will answer questions about any medications they are taking and whether they have any adverse events.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Szacowany)
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Bayer Clinical Trials Contact
- Numer telefonu: 0018888422937
- E-mail: clinical-trials-contact@bayer.com
Lokalizacje studiów
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Multiple Locations, Korea Południowa
- Rekrutacyjny
- Many locations
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
Patients who have been prescribed Darolutamide for a medically appropriate use will be eligible to be enrolled.
Opis
Inclusion Criteria:
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Male aged ≥19 years
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Patients with high risk nmCPRC
- Castrate level of serum testosterone (< 1.7 nmol/l [50 ng/dL])
- PSA doubling time < 10 months
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Patients with mHSPC
- histologically or cytologically confirmed prostate cancer, and metastases detected on bone scanning, contrast-enhanced computed tomography (CT), or magnetic resonance imaging (MRI).
- be candidates for androgen-deprivation therapy with/without docetaxel.
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Patients for whom the decision to initiate treatment with Darolutamide as a first time was made as per investigator's routine treatment practice
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Written informed consent from subject or legal representative; assent from subject when appropriate
Exclusion Criteria:
- Patients participating in an investigational program with interventions outside of routine clinical practice
- Participants with contraindication according to the locally approved prescribing information
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Modele obserwacyjne: COHORT
- Perspektywy czasowe: PROSPECTIVE
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
|---|---|
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Male patients with nmCRPC or mHSPC
Male patients with a diagnosis of non-metastatic castration-resistant prostate cancer (nmCRPC) or metastatic hormone-sensitive prostate cancer (mHSPC) will be enrolled after the decision for treatment with Darolutamide has been made by the investigator. |
The decision on the dose and duration of treatment is solely at the discretion of the treating physician, based on the recommendations written in the local product information. |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Number, severity of adverse events (including SAEs)
Ramy czasowe: From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
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SAE stands for serious adverse event. An adverse event (AE) is any untoward medical occurrence in a patient administered a medicinal product and which does not necessarily have a causal relationship with this treatment. |
From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
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Number, severity of adverse drug reactions (including SADRs)
Ramy czasowe: From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
|
SADR stands for serious adverse drug reaction. An ADR is any AE judged by investigator as having a reasonable suspected causal relationship to Darolutamide. |
From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
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The outcome of (serious) adverse events
Ramy czasowe: From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
|
An adverse event (AE) is any untoward medical occurrence in a patient administered a medicinal product and which does not necessarily have a causal relationship with this treatment. |
From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
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The outcome of (serious) adverse drug reactions
Ramy czasowe: From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
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An ADR is any AE judged by investigator as having a reasonable suspected causal relationship to Darolutamide. |
From the date that the patient signed the informed consent to 30 days after the end of the treatment (up to 52 weeks)
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Powody zakończenia stosowania darolutamidu
Ramy czasowe: Do 52 tygodnia
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Do 52 tygodnia
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Dawkowanie i modyfikacja dawki darolutamidu
Ramy czasowe: Do 52 tygodnia
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Do 52 tygodnia
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Metastasis-free survival (MFS) by nmCRPC indication
Ramy czasowe: Up to 52 weeks
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MFS is defined as the time (months) from the initiation of Darolutamide treatment to the date of first observed metastasis. |
Up to 52 weeks
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Time to first symptomatic skeletal event (SSE) by nmCRPC indication
Ramy czasowe: Up to 52 weeks
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Time to SSE is defined as the time (months) from the initiation of Darolutamide treatment to the date of first diagnosed skeletal-related event. |
Up to 52 weeks
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Time to prostate-specific antigen (PSA) progression by nmCRPC indication
Ramy czasowe: Up to 52 weeks
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Time to PSA progression is defined as the time (months) from the initiation of Darolutamide treatment to the date at which PSA is recorded at ≥25% increase above the nadir (lowest screening or baseline) value along with an increase in absolute value of ≥2 ng/mL above nadir. |
Up to 52 weeks
|
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Overall survival by nmCRPC indication
Ramy czasowe: Up to 52 weeks
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Overall survival is defined as the time (months) from the initiation of Darolutamide treatment until death from any cause. |
Up to 52 weeks
|
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Time to Castration-Resistant Prostate Cancer (CRPC) by mHSPC indication
Ramy czasowe: Up to 52 weeks
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Time to mCRPC, defined as the time to PSA progression with serum testosterone being at castrate level <0.50 ng/mL, or the time to progression by soft tissue/visceral lesions or time to progression by bone lesions, whatever comes first. |
Up to 52 weeks
|
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Time to first symptomatic skeletal event (SSE) by mHSPC indication
Ramy czasowe: Up to 52 weeks
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Time to SSE is defined as the time (months) from the initiation of Darolutamide treatment to the date of first diagnosed skeletal-related event. |
Up to 52 weeks
|
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Time to prostate-specific antigen (PSA) progression by mHSPC indication
Ramy czasowe: Up to 52 weeks
|
Time to PSA progression is defined as the time (months) from the initiation of Darolutamide treatment to the date at which PSA is recorded at ≥25% increase above the nadir (lowest screening or baseline) value along with an increase in absolute value of ≥2 ng/mL above nadir. |
Up to 52 weeks
|
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Overall survival by mHSPC indication
Ramy czasowe: Up to 52 weeks
|
Overall survival is defined as the time (months) from the initiation of Darolutamide treatment until death from any cause. |
Up to 52 weeks
|
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Time to initiation of subsequent anti-cancer therapy by mHSPC indication
Ramy czasowe: Up to 52 weeks
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Time to initiation of subsequent anti-cancer therapy is defined as the time (months) from the initiation of Darolutamide treatment to the date of first administration of any subsequent anti-cancer therapy after discontinuation of Darolutamide. |
Up to 52 weeks
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Radiological progression (Soft tissue/ Bone metastasis) by mHSPC indication
Ramy czasowe: Up to 52 weeks
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Radiological progression is defined as the time (months) from the start of Darolutamide treatment to the date of first documentation of radiological progressive disease or death due to any cause, whichever occurs first. |
Up to 52 weeks
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Radiological Progression-Free Survival (rPFS) by mHSPC indication
Ramy czasowe: Up to 52 weeks
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Radiographic Progression-Free Survival (rPFS) is defined as the time (months) from the initiation of Darolutamide treatment to the date of the first radiologically confirmed disease progression or death from any cause, whichever occurs first. |
Up to 52 weeks
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Duration of Darolutamide treatment
Ramy czasowe: Up to 52 weeks
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Duration of Darolutamide treatment is defined as the time (months) from the start of Darolutamide treatment to the day of permanent discontinuation of Darolutamide (including death). |
Up to 52 weeks
|
Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 20654
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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