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NCT07028853 · ClinicalTrials.gov registry record · Phase 3

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.

A Phase 3 study of Prostate Cancer and Cancer of the Prostate, sponsored by Pfizer.

Recruiting
Registry status
Phase 3
Development phase
1,000
Enrollment target
20
Study locations

NCT07028853: Recruiting Phase 3 study of Prostate Cancer and Cancer of the Prostate, sponsored by Pfizer.

NCT07028853 is a Phase 3 study of Prostate Cancer and Cancer of the Prostate that is actively recruiting participants, run by Pfizer. The registered enrollment target is 1,000 participants, above the 607-participant average among 735 other Prostate Cancer trials with a reported enrollment target (65% higher). The trial reports 20 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07028853, a Phase 3 study of Prostate Cancer and Cancer of the Prostate, is actively recruiting participants, sponsored by Pfizer.

RECRUITING
Registry status
Phase 3
Development phase
1,000 participants
Enrollment target
20
Study locations

Study 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.

Primary Outcome

rPFS is defined as the time from randomization until PD based on BICR assessment per RECIST v1.1 (soft tissue disease) and PCWG3 (bone disease), or death due to any cause, whichever occurs first.

Interventions

  • DRUG Placebo
  • DRUG Enzalutamide
  • DRUG Mevrometostat

Study Locations (20)

California

  • UCLA Hematology/Oncology - Alhambra - Alhambra
  • UCLA Hematology/Oncology - Atascadero - Atascadero
  • UCLA Hematology/Oncology - Beverly Hills - Beverly Hills
  • UCLA Hematology/Oncology - Burbank - Burbank
  • UCLA Hematology/Oncology - Encino - Encino
  • UCLA Hematology/Oncology - Irvine - Irvine
  • UCLA Hematology/Oncology - Laguna Hills - Laguna Hills
  • Ronald Reagan UCLA Medical Center - Drug Information Center - Los Angeles
  • UCLA Department of Medicine - Hematology/Oncology - Los Angeles

Arizona

  • Ironwood Cancer & Research Centers - Chandler
  • Ironwood Cancer & Research Centers - Gilbert
  • Ironwood Cancer & Research Centers - Glendale
  • Ironwood Cancer & Research Centers - Goodyear
  • Ironwood Cancer & Research Centers - Mesa
  • Ironwood Cancer & Research Centers - Mesa
  • Ironwood Cancer & Research Centers - Phoenix
  • Ironwood Cancer & Research Centers - Scottsdale

Arkansas

  • Highlands Oncology Group, PA - Fayetteville
  • Highlands Oncology Group, PA - Rogers
  • Highlands Oncology Group, PA - Springdale

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2025-09-28
Est. Completion 2034-12-08
Phase Phase 3
Pfizer

1,845 total trials

What NCT07028853 shows while recruiting

NCT07028853 is an interventional study that assigns participants to a tested intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus, above the 607-participant average among 735 other Prostate Cancer trials with a reported enrollment target (65% higher).

The record links to 4 conditions, with Prostate Cancer appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT07028853 names 20 study sites across 3 states, led by California, Arizona, Arkansas.

Frequently Asked Questions

What is clinical trial NCT07028853 about?

NCT07028853 is a clinical study titled "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.". 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.

What is the current status of trial NCT07028853?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 1,000 participants. The study started on 2025-09-28. Estimated completion is 2034-12-08.

What conditions does trial NCT07028853 study?

This clinical trial studies the following conditions: Prostate Cancer, Cancer of the Prostate, Hormone Sensitive Prostate Cancer, Metastatic Castration Sensitive Prostate Cancer (mCSPC).

What interventions are being tested in trial NCT07028853?

The interventions under investigation include: Placebo (DRUG), Enzalutamide (DRUG), Mevrometostat (DRUG).

Who is sponsoring clinical trial NCT07028853?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07028853 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Prostate Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07028853's enrollment target sits among peer trials

1,000 59th of 735 higher than 669 of 735 other Prostate Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Prostate Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07028853, the US trial registry maintained by the National Library of Medicine. NCT07028853 (large enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.