Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Recruiting Phase 1

A Study of Valemetostat (DS-3201b) in Combination With Darolutamide in Metastatic Castration Resistant Prostate Cancer (mCRPC)

NCT07244341 · tracked via the Priya Life Science Japan tracker
Phase
Phase 1
Started
2025-12-03
Last updated
2026-05-15

Condition(s) studied

Metastatic Castration-resistant Prostate Cancer

Investigational drug(s) / intervention(s)

Valemetostat →Darolutamide →

Valemetostat: Dose Escalation Part: Valemetostat will be administered at escalating doses. Dose Expansion Part: Valemetostat will be administered at 2 or more dose levels.

Darolutamide: Dose Escalation Part: Darolutamide will be administered at a standard dose. Dose Expansion Part: Darolutamide will be administered at a standard dose.

Study summary

This study will assess the safety and tolerability of valemetostat in combination with darolutamide in participants with Metastatic Castration Resistant Prostate Cancer (mCRPC).

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria: The clinical site will screen for the full inclusion criteria per protocol. 1. Adult males ≥18 years of age at the time the ICF is signed (Please follow local regulatory requirements if the legal age of consent for trial participation is \>18 years old). 2. Histologically confirmed adenocarcinoma of the prostate. Cases exhibiting neuroendocrine differentiation are eligible for enrollment, except those with a diagnosis of pure small cell carcinoma, which is excluded. 3. Evidence of disease progression as per the PCWG3 modified RECIST v1.1 criteria. 4. Evidence of metastatic disease as confirmed by radiographic imaging (CT, MRI, or bone scan). 5. Ongoing androgen deprivation at time of enrollment. • For participants currently being treated with luteinizing hormone-releasing hormone agonists or antagonists, therapy must have been initiated at least 4 weeks prior to enrollment and treatment must be continued throughout the trial. 6. Baseline PSA expression level of ≥2 ng/mL, according to a documented testing result. 7. Prior therapy with an Androgen Receptor Pathway Inhibitors (ARPI). 8. ECOG PS of 0 or 1 assessed no more than 28 days prior to enrollment. 9. Is willing and able to provide adequate fresh or archival tumor samples with sufficient quantity and tissue quality. A mandatory newly obtained pretreatment biopsy is required, if not clinically contraindicated and at an acceptable risk as determined by the investigator. If newly obtained tissue samples are not possible to obtain, archival tissue obtained from a lesion not previously irradiated and collected after the most recent prior therapy is acceptable. 10. A male participant capable of producing sperm is eligible to participate if he agrees to the following during the intervention period and for at least the time needed to eliminate each trial intervention. The length of time required to continue contraception after the last dose for each trial intervention is 3 months. * Must not freeze or donate sperm starting at screening and throughout the Treatment Period, and for at least 3 months after the final trial intervention administration. Note: Preservation of sperm should be considered before enrollment in this trial. • Adhere to either of the following contraception methods: * True abstinence from penile-vaginal intercourse, when this is in line with the preferred and usual lifestyle of the participant, OR * Uses a penile/external condom when having penile-vaginal intercourse with an NPOCBP, PLUS partner use of an additional contraceptive method, as a condom may break or leak Contraceptive use should be consistent with local regulations regarding the methods of contraception for those participating in clinical trials. If the contraception requirements in the local label for any trial interventions are more stringent than those above, the local label requirements are to be followed. Key Exclusion Criteria: The clinical site will screen for the full exclusion criteria per protocol. 1. Prior treatment with any epigenetic agents including but not limited to EZH1, EZH2, EZH1/2, or PRC2 inhibitors. 2. Has a super scan as seen in the baseline bone scan. A super scan is defined as an intense symmetric activity in the bones and diminished renal parenchymal activity on baseline bone scan, such that the presence of additional metastases in the future could not be evaluated. 3. Clinically active brain metastases, spinal cord compression, or leptomeningeal carcinomatosis, defined as untreated or symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms. 4. Uncontrolled or significant cardiovascular disease, 5. Prior malignancy, active within the previous 3 years except for locally curable cancers that have been apparently cured or successfully resected, such as basal or squamous cell carcinoma, superficial bladder cancer, carcinoma in situ of the stomach, or carcinoma in situ of the breast. 6. Has active or uncontrolled HBV infection. 7. Has active or uncontrolled HCV infection. 8. Has active or uncontrolled HIV infection.

Primary outcome measure(s)

  • Part 1: Number of participants with Dose-Limiting Toxicities (DLTs) — Day 1 up to Day 28
    A DLT is defined as any Treatment Emergent Adverse Event (TEAE) not attributable to disease or disease-related processes, environmental factors, unrelated trauma, etc, that occurs during the DLT evaluation period (Day 1 to Day 28) and is Grade ≥3.
  • Part 1 and 2: Number of Participants Experiencing a Treatment Emergent Adverse Event (TEAE) — From Screening up to approximately 5 years
    TEAEs are defined as those Adverse Events (AEs) with start or worsening date during the on-treatment period (from the first dose date of trial intervention to 30 days after the last dose date of trial intervention).

Trial sites (19)

FacilityCityRegionStatus
University of California San Diego Moores Cancer Center La Jolla California Recruiting
Beth Isreal Deaconess Medical Center Boston Massachusetts Recruiting
Dana Farber Cancer Institute Newton Massachusetts Recruiting
Cancer & Hematology Center Grand Rapids Michigan Recruiting
Northwell Health Cancer Institute (START NY) Lake Success New York Recruiting
Carolina Urologic Research Center Myrtle Beach South Carolina Recruiting
NEXT Oncology San Antonio Texas Recruiting
Virginia Cancer Specialists (NEXT Virginia) Fairfax Virginia Recruiting
Medical College Of Wisconsin Milwaukee Wisconsin Recruiting
Sun Yatsen University Cancer Center Guangzhou China Recruiting
Fudan University Shanghai Cancer Center - Xuhui District Shanghai China Recruiting
Fudan University Shanghai Cancer Center Shanghai China Recruiting
Shanghai General Hospital Shanghai China Recruiting
The First Affiliated Hospital of Wenzhou Medical University Wenzhou China Recruiting
Mater Misericordiae University Hospital Dublin Ireland Recruiting
National Cancer Center Hospital East Kashiwa-shi Japan Recruiting
Kobe City Med Cen Gen Hosp. Kobe Japan Recruiting
Cancer Institute Hospital of JFCR Kōtoku Japan Recruiting
Toho University Sakura Medical Center Sakura-shi Japan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07244341 on ClinicalTrials.gov ↗ ← All trials in Japan