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This Study Will Explore Whether a Combination of the Investigational Drug Mevrometostat (PF-06821497) and Enzalutamide Will Work Better Than Taking Enzalutamide Alone in Participants With mCSPC Who Are ARPI naïve.
RECRUITINGPhase 3Sponsored by Pfizer
Actively Recruiting
PhasePhase 3
SponsorPfizer
Started2025-09-28
Est. completion2028-09-12
Eligibility
Age18 Years+
SexMALE
Healthy vol.Accepted
Locations46 sites
View on ClinicalTrials.gov →
NCT07028853
Summary
This study will explore whether a combination of the investigational drug mevrometostat (PF-06821497) and enzalutamide will work better than taking enzalutamide alone in participants with mCSPC who are ARPI naïve and have not yet received chemotherapy in the mCSPC setting.
Eligibility
Age: 18 Years+Sex: MALEHealthy volunteers accepted
Inclusion Criteria * Male participants aged ≥18 years (or the minimum age of consent in accordance with local regulations) at screening. * Histologically or cytologically confirmed adenocarcinoma of the prostate without small cell features. * Metastatic prostate cancer documented by positive bone scan (for bone disease) or metastatic lesion(s) on CT or MRI (for soft tissue/visceral disease). * Resolution of acute effects of any prior therapy to either baseline severity or CTCAE Grade ≤1 (except for AEs which do not constitute a safety risk in the investigator's judgement). * Participants must have ECOG PS 0 or 1. Exclusion Criteria * Any medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study. * Clinically significant cardiovascular disease. * Known or suspected brain metastasis or active leptomeningeal disease. * Participants must be treatment naïve at the mCSPC stage, eg, participants cannot have received any cytotoxic chemotherapy with the following exceptions: Treatment with first-generation antiandrogen (ADT) agents is allowed for mCSPC. * Previous administration with an investigational product (drug or vaccine) within 30 days. * Current use or anticipated need for drugs that are known strong CYP3A4/5 inhibitors and inducers (with exception of enzalutamide as part of this study). * Inadequate organ function.
Conditions5
CancerCancer of the ProstateHormone Sensitive Prostate CancerMetastatic Castration Sensitive Prostate Cancer (mCSPC)Prostate Cancer
Locations46 sites
Ironwood Cancer & Research Centers
Chandler, Arizona, 85224
Ironwood Cancer & Research Centers
Gilbert, Arizona, 85297
Ironwood Cancer & Research Centers
Glendale, Arizona, 85306
Ironwood Cancer & Research Centers
Goodyear, Arizona, 85395
Ironwood Cancer & Research Centers
Mesa, Arizona, 85202
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Actively Recruiting
PhasePhase 3
SponsorPfizer
Started2025-09-28
Est. completion2028-09-12
Eligibility
Age18 Years+
SexMALE
Healthy vol.Accepted
Locations46 sites
View on ClinicalTrials.gov →
NCT07028853