This study will assess the safety and tolerability of valemetostat in combination with darolutamide in participants with Metastatic Castration Resistant Prostate Cancer (mCRPC).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Dose Escalation Part: Valemetostat will be administered at escalating doses. Dose Expansion Part: Valemetostat will be administered at 2 or more dose levels.
Dose Escalation Part: Darolutamide will be administered at a standard dose. Dose Expansion Part: Darolutamide will be administered at a standard dose.
University of California San Diego Moores Cancer Center
La Jolla, California, United States
Part 1: Number of participants with Dose-Limiting Toxicities (DLTs)
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.
Time frame: Day 1 up to Day 28
Part 1 and 2: Number of Participants Experiencing a Treatment Emergent Adverse Event (TEAE)
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).
Time frame: From Screening up to approximately 5 years
Prostate-Specific Antigen (PSA) 50 Response Rate
PSA50 response rate is defined as the percentage of participants who achieved a decline in PSA percent change from baseline by at least 50%, with a consecutive confirmation assessment at least 3 weeks later per the PCWG3 modified RECIST v1.1 criteria.
Time frame: From Screening up to approximately 5 years
Prostate-Specific Antigen (PSA) 90 Response Rate
PSA90 response rate is defined as the percentage of participants who achieved a decline in PSA percent change from baseline by at least 90%, with a consecutive confirmation assessment at least 3 weeks later per the PCWG3 modified RECIST v1.1 criteria.
Time frame: From Screening up to approximately 5 years
Prostate-Specific Antigen (PSA) Nadir Response Rate
PSA nadir response rate is defined as the proportion of participants who achieve a PSA level of ≤ 0.2 ng/mL at any time during the Treatment Period.
Time frame: From Screening up to approximately 5 years
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Beth Isreal Deaconess Medical Center
Boston, Massachusetts, United States
RECRUITINGDana Farber Cancer Institute
Newton, Massachusetts, United States
RECRUITINGCancer & Hematology Center
Grand Rapids, Michigan, United States
RECRUITINGNorthwell Health Cancer Institute (START NY)
Lake Success, New York, United States
RECRUITINGCarolina Urologic Research Center
Myrtle Beach, South Carolina, United States
RECRUITINGNEXT Oncology
San Antonio, Texas, United States
RECRUITINGVirginia Cancer Specialists (NEXT Virginia)
Fairfax, Virginia, United States
RECRUITINGMedical College Of Wisconsin
Milwaukee, Wisconsin, United States
RECRUITINGSun Yatsen University Cancer Center
Guangzhou, China
RECRUITING...and 9 more locations
Radiographic Progression-Free Survival (rPFS)
rPFS is defined as the time (month) from the start date of trial intervention to the earlier date of the first objective documentation of radiographic disease progression as assessed by the investigator based on the PCWG3 modified RECIST v1.1 criteria or death due to any cause.
Time frame: From Screening up to approximately 5 years
Overall Survival (OS)
OS is defined as the time (month) from the start date of trial intervention to the date of death due to any cause.
Time frame: From Screening up to approximately 5 years
Time to PSA Progression
Time to PSA progression is defined as the time interval from the start date of trial intervention to PSA progression, per the PCWG3 modified RECIST v1.1 criteria. PSA progression is defined as: * A ≥25% increase and an absolute increase of ≥2 ng/mL from the nadir, confirmed by a second PSA measurement obtained at least 3 weeks later, in participants who experience a decline in PSA from baseline; OR * A ≥25% increase and an absolute increase of ≥2 ng/mL from baseline, occurring beyond 12 weeks from treatment initiation, in participants who do not experience a PSA decline from baseline.
Time frame: From Screening up to approximately 5 years
Objective Response Rate (ORR)
ORR is defined as the proportion of participants with measurable disease who achieved a BOR of confirmed CR or confirmed PR as assessed by the investigator according to the PCWG3 modified RECIST v1.1 criteria.
Time frame: From Screening up to approximately 5 years
Time to First SSRE (symptomatic bone fractures, spinal cord compression, surgery, or radiation to the bone, whichever is first)
Time to first SSRE (symptomatic bone fractures, spinal cord compression, surgery, or radiation to the bone, whichever is first) is defined as the time interval from the start date of trial intervention to the date of the first observed SSRE.
Time frame: From Screening up to approximately 5 years
Total and Unbound Plasma Concentration of Valemetostat in Combination with Darolutamide
Time frame: Cycle 1: Day 1, Day 8, Day 15. Cycles 2-5: Day 1 (Each cycle is 28 days)