Study Comparing MK-5684 with Abiraterone Acetate or Enzalutamide for Patients with Advanced Prostate Cancer After Hormonal Therapy and Chemotherapy

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What is this study about?

This clinical trial is focused on studying a condition known as metastatic castration-resistant prostate cancer (mCRPC). This is a type of prostate cancer that continues to grow and spread even when the amount of male hormones in the body is reduced to very low levels. The study is comparing a new treatment called MK-5684 with two existing medications, abiraterone acetate and enzalutamide, which are already used to treat this type of cancer. The purpose of the study is to see how well MK-5684 works compared to the other two medications in terms of helping patients live longer and slowing down the progression of the cancer.

Participants in the study will receive either MK-5684 or one of the approved medications, abiraterone acetate or enzalutamide. The study will monitor the participants over a period to assess their overall survival and the progression of their cancer. The study will also look at other factors such as the time it takes for the cancer to progress, the response to the treatment, and any side effects experienced by the participants. The study aims to provide valuable information on the effectiveness and safety of MK-5684 as a potential treatment option for patients with mCRPC.

Throughout the study, participants will be closely monitored by healthcare professionals to ensure their safety and to gather data on the treatment’s impact. The study will help determine if MK-5684 can offer a new and effective treatment option for those with advanced prostate cancer who have already undergone hormonal therapy and chemotherapy. This research is important for advancing the understanding and treatment of metastatic castration-resistant prostate cancer.

1 joining the study

Upon joining the study, the participant will be randomly assigned to receive either the new treatment MK-5684 or an alternative approved medication, which could be abiraterone acetate or enzalutamide.

The assignment is open-label, meaning both the participant and the study team will know which treatment is being administered.

2 treatment administration

Participants receiving MK-5684 will take the medication orally as directed by the study protocol.

Participants assigned to abiraterone acetate will take the medication orally, typically once daily, as per standard dosing guidelines.

Participants assigned to enzalutamide will also take the medication orally, usually once daily, following standard dosing instructions.

3 monitoring and assessments

Regular monitoring will occur to assess the participant’s health and response to the treatment. This includes blood tests, imaging studies, and other necessary evaluations.

Participants will be assessed for overall survival and progression-free survival, which measures the time during and after treatment that the participant lives with the disease without it getting worse.

4 follow-up

After completing the treatment phase, participants will enter a follow-up period where their health and any long-term effects of the treatment will be monitored.

The follow-up period will include regular check-ups and assessments to ensure the participant’s well-being and to gather data on the long-term efficacy and safety of the treatment.

Who Can Join the Study?

  • The patient must have a confirmed type of prostate cancer called adenocarcinoma, which is not a small cell type.
  • The patient must provide a sample of tumor tissue from a recent biopsy that was not previously treated with radiation.
  • If the patient is infected with HIV, their condition must be well controlled with medication.
  • The patient must have a performance status of 0 or 1, which means they are fully active or have some symptoms but can still do light work.
  • If the patient has hepatitis B, they must have been treated for at least 4 weeks and have no detectable virus in their blood.
  • If the patient had hepatitis C, the virus must not be detectable in their blood at the time of screening.
  • The patient’s prostate cancer must have worsened while on hormone therapy or after surgical removal of the testicles within 6 months before screening.
  • If the patient used certain anti-androgen medications, their disease must have worsened more than 4 weeks after stopping flutamide and more than 6 weeks after stopping bicalutamide or nilutamide.
  • The patient must have evidence of cancer that has spread to other parts of the body, shown by bone or soft tissue scans.
  • The patient’s disease must have worsened during or after treatment with one new type of hormone therapy.
  • The patient must have received one or two chemotherapy treatments based on taxane for their cancer and have had disease progression during or after these treatments.
  • The patient must continue hormone therapy to keep testosterone levels below 50 ng/dL.
  • If the patient is receiving treatment to prevent bone loss, they must have been on a stable dose for at least 4 weeks before starting the study.
  • If the patient can produce sperm, they must agree not to donate sperm and either abstain from sex or use a condom during the study and for a specified time after the last dose of study medication.

Who Cannot Join the Study?

  • Patients who have a different type of cancer other than metastatic castration-resistant prostate cancer cannot participate. This type of cancer is a form of prostate cancer that has spread to other parts of the body and does not respond to treatments that lower testosterone.
  • Patients who are female cannot participate, as the study is only for male patients.
  • Patients who are considered part of a vulnerable population, such as those who cannot give consent or are unable to understand the study, are not eligible.
  • Patients who are not within the specified age range for the study cannot participate. The study is for adults, typically those who are older.
  • Patients who have not been diagnosed with the specific condition being studied, which is metastatic castration-resistant prostate cancer, are not eligible.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Institut Gustave Roussy Villejuif France
Kuopio University Hospital Kuopio Finland
Szpital Wojewodzki Im. Mikolaja Kopernika W Koszalinie Koszalin Poland
Zuyderland Medisch Centrum Stichting Geleen The Netherlands
Centre Jean Perrin Clermont Ferrand France
Frisius Heerenveen The Netherlands
University Hospital Jena KöR Jena Germany
Medical University Of Graz Graz Austria
Hospital Jerez de la Frontera Jerez De La Frontera Spain

Other Sites

Site Name City Country Status
Haga Hospital Hague The Netherlands
Orszagos Onkologiai Intezet Budapest Hungary
Centrum Onkologii Im. Prof. Franciszka Lukaszczyka W Bydgoszczy Bydgoszcz Poland
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Centre Hospitalier Universitaire De Nimes Nimes France
Hospital Universitario 12 De Octubre Madrid Spain
Klinikum Wels-Grieskirchen GmbH Wels Austria
Masarykuv Onkologicky Ustav Brno-Stred Czechia
St. Olavs Hospital HF Trondheim Norway
Fundacion Instituto Valenciano De Oncologia Valencia Spain
Stichting Viecuri Medisch Centrum voor Noord-Limburg Venlo The Netherlands
Mazowiecki Szpital Wojewodzki Im. Sw. Jana Pawła II W Siedlcach Sp. z o.o. Siedlce Poland
HELIOS Kliniken Schwerin GmbH Schwerin Germany
University Of Debrecen Debrecen Hungary
Zachodniopomorskie Centrum Onkologii Szczecin Poland
Virgen del Rocío University Hospital Sevilla Spain
Odense University Hospital Odense Denmark
Ospedale San Raffaele S.r.l. Milan Italy
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Karolinska University Hospital Solna Sweden
Stichting Radboud University Medical Center Nijmegen The Netherlands
Meander Medical Center Amersfoort The Netherlands
Turku University Hospital Turku Finland
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Sint Franciscus Vlietland Groep Stichting Rotterdam The Netherlands
Centre Hospitalier De La Cote Basque Bayonne France
Sykehuset Oestfold HF Kalnes Graalum Norway
Hospital Universitario Lucus Augusti Lugo Spain
Swietokrzyskie Centrum Onkologii Samodzielny Publiczny Zaklad Opieki Zdrowotnej W Kielcach Kielce Poland
St Vincent’s University Hospital Dublin Ireland
University Hospital Olomouc Olomouc Czechia
Rigshospitalet Copenhagen Denmark
Pirkanmaan hyvinvointialue Tampere Finland
Netherlands Cancer Institute Amsterdam The Netherlands
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Hopital Beaujon Clichy France
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Spaarne Gasthuis Hoofddorp The Netherlands
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
University Hospital Ostrava Ostrava Czechia
Centre De Lutte Contre Le Cancer Eugene Marquis Rennes France
Ulxwrfbfpy Maybpdv Cgcbxb Hrypcyacwrcamdfoz Hamburg Germany
Onkakpwvvnfcke Lqdg Gvmr Linz Austria
Rwannxobnr Svjqwjd Sujbhphfxeftujs Ibr Dxz Wqszhmdfmh Bbklvwiotame Grudziadz Poland
Njbsfp Vvvgoyyvc Shfjk Ljmnp Kumeoo Salgotarjan Hungary
Bqctevjopug Vlsjosecy Olrlabsfsrod Kecskemet Hungary
Fdifmbkv nbmxcyxqw Mvvhu a Hdjznkf Prague Czechia
Ibkcwmyx Rfbiirayf Pgz Lm Shvmpw Dml Towhmg Dwky Abduuzy Itrq Srxxnm Meldola Italy
Awzcsszwe Ucm Amsterdam The Netherlands
Alslyddq Ukazmbjehw Hzpcsrof Lorenskog Norway
Ujrdhvw Uhvqldkqxq Hjbctaop Uppsala Sweden
Svp Euwvtjwyz Hpnvrvaa Tlsjotf Tilburg The Netherlands
Uogrtantztahvrvukmrhz Mzqklaay Ato Munster Germany
Cakmxr Okkgt Llrvffs Lille France
Hwmxwyiu Ufsgnzhyfmkgos Sdqqnlwqjm &cprrbh Hqhbeoz du Hvpoolutlbd STRASBOURG, Alsace France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Recruiting
01.03.2024
Czechia Czechia
Recruiting
01.03.2024
Denmark Denmark
Recruiting
01.03.2024
Finland Finland
Recruiting
01.03.2024
France France
Recruiting
01.03.2024
Germany Germany
Recruiting
01.03.2024
Hungary Hungary
Recruiting
01.03.2024
Ireland Ireland
Recruiting
01.03.2024
Italy Italy
Recruiting
01.03.2024
Norway Norway
Recruiting
01.03.2024
Poland Poland
Recruiting
01.03.2024
Spain Spain
Recruiting
01.03.2024
Sweden Sweden
Recruiting
01.03.2024
The Netherlands The Netherlands
Recruiting
01.03.2024

Trial locations

MK-5684 is an investigational medication being studied for its potential to improve survival in patients with metastatic castration-resistant prostate cancer (mCRPC). It is being compared to other treatments to see if it can help patients live longer and slow down the progression of the disease.

Abiraterone Acetate is a medication used to treat prostate cancer by lowering the levels of male hormones in the body, which can help slow the growth of cancer cells. In this study, it is used as a comparison treatment to evaluate the effectiveness of MK-5684.

Enzalutamide is another treatment option for prostate cancer that works by blocking the effects of male hormones on cancer cells, helping to slow their growth. It is also used in this trial as a comparison to assess the benefits of MK-5684.

Metastatic Castration-Resistant Prostate Cancer – This is a type of prostate cancer that continues to grow and spread even when the amount of testosterone in the body is reduced to very low levels. It is characterized by cancer cells that have spread beyond the prostate gland to other parts of the body, such as bones or lymph nodes. The disease progresses despite hormonal therapy aimed at lowering testosterone, which is typically used to control prostate cancer growth. Over time, the cancer cells adapt and continue to thrive without the need for high levels of androgens, which are male hormones. This condition is often associated with mutations in the androgen receptor, which can affect the cancer’s response to treatment. The progression of the disease can lead to various symptoms, including pain and complications related to the spread of cancer to other organs.

Trial ID:
2023-504899-25-00
Protocol code:
MK-5684-003
NCT ID:
NCT06136624
Trial Phase:
Therapeutic confirmatory (Phase III)

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