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Recruiting Phase 1 Interventional

A Study of Mevrometostat for Treatment of Relapsed/Refractory SCLC, Castration Resistant Prostate Cancer, and Follicular Lymphoma

ClinicalTrials.gov ID: NCT03460977

Public ClinicalTrials.gov record NCT03460977. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 5:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A PHASE I DOSE ESCALATION AND EXPANDED COHORT STUDY OF PF 06821497 (MEVROMETOSTAT) IN THE TREATMENT OF ADULT PATIENTS WITH RELAPSED/REFRACTORY SMALL CELL LUNG CANCER (SCLC), CASTRATION RESISTANT PROSTATE CANCER (CRPC) AND FOLLICULAR LYMPHOMA (FL)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to learn about the safety and effects of the study medicine (called Mevrometostat) for the possible treatment of Relapsed/ Refractory Small Cell Lung Cancer (SCLC), Castration Resistant Prostate Cancer (CRPC) and Follicular Lymphoma (FL). The study consists of 3 parts; Part 1 and 2 enrolled participants with SCLC, metastatic CRPC, and FL are closed for enrollment. Part 3, which is open for enrollment is seeking men who: * have Castration Resistant Prostate Cancer (CRPC) and * have previously received treatment for CRPC and have progressed from the last treatment All participants in Part 3 of this study will receive mevrometostat and/ or enzalutamide. Part 3 consists of 2 sub studies each has an assessment phase and a maintenance phase. The Part 3 DDI substudy consist of 2 cohorts, Cohort 1 (monotherapy cohort) and Cohort 2 (Combination cohort). In the assessment phase: * participants in the BE substudy will take 3 single doses of mevrometostat by mouth over 3 periods. * participants in the DDI substudy Cohort 1 (monotherapy cohort) will take mevrometostat 2 times a day and/or itraconazole 1 time a day based on a present schedule. * participants in the DDI substudy Cohort 2 (combination cohort) will take mevrometostat 2 times a day, enzalutamide 1 time a day, and/or itraconazole 1 time a day based on a present schedule. After completion of the assessment phase, participants will enter the maintenance phase where they will receive mevrometostat 2 times a day and enzalutamide 1 time a day by mouth until their cancer is no longer responding. The study will look at the experiences of participanrs receiving the study medicine. This will help see if the study medicine is safe and effective.

Study identification

NCT ID
NCT03460977
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
453 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 16, 2018
Primary completion
Apr 19, 2028
Completion
Jul 6, 2029
Last update posted
Aug 23, 2026

2018 – 2029

United States locations

U.S. sites
44
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Banner-University Medical Center Tucson Tucson Arizona 85719 Active, not recruiting
The University of Arizona Cancer Center-North Campus Tucson Arizona 85719 Active, not recruiting
The University of Arizona Cancer Center Tucson Arizona 85724 Active, not recruiting
Arizona Urology Specialists, PLLC Tucson Arizona 85741 Terminated
Pacific Cancer Medical Center INC Anaheim California 92801 Active, not recruiting
City of Hope (City of Hope National Medical Center, City of Hope Medical Center) Duarte California 91010 Active, not recruiting
City of Hope Investigational Drug Services (IDS) Duarte California 91010 Active, not recruiting
Norwalk Hospital Norwalk Connecticut 06856 Active, not recruiting
The University of Kansas Cancer Center, Investigational Drug Services Fairway Kansas 66205 Active, not recruiting
The University of Kansas Clinical Research Center Fairway Kansas 66205 Active, not recruiting
The University of Kansas Hospital Kansas City Kansas 66160 Active, not recruiting
The University of Kansas Medical Center Medical Office Building Kansas City Kansas 66160 Active, not recruiting
The University of Kansas Cancer Center - Indian Creek Campus Overland Park Kansas 66211 Active, not recruiting
The University of Kansas Cancer Center Westwood Kansas 66205 Active, not recruiting
Norton Cancer Institute - Downtown Louisville Kentucky 40202 Active, not recruiting
Norton Cancer Institute, Norton Healthcare Pavilion Louisville Kentucky 40202 Active, not recruiting
Norton Hospital Louisville Kentucky 40202 Active, not recruiting
Maryland Oncology Hematology, P.A. Rockville Maryland 20850 Terminated
Brigham and Women's Hospital Boston Massachusetts 02115 Active, not recruiting
Dana Farber Cancer Institute Boston Massachusetts 02215 Active, not recruiting
Dana Farber Cancer Institute- Chestnut Hill Newton Massachusetts 02459 Active, not recruiting
Oncology Hematology West, PC dba Nebraska Cancer Specialists Omaha Nebraska 68130 Recruiting
Hackensack University Medical Center Hackensack New Jersey 07601 Active, not recruiting
John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601 Active, not recruiting
OU Health University of Oklahoma Medical Center Oklahoma City Oklahoma 73104 Recruiting
Stephenson Cancer Center (chemo location) Oklahoma City Oklahoma 73104 Recruiting
Carolina Urologic Research Center Myrtle Beach South Carolina 29572 Recruiting
Parkway Surgery Center Myrtle Beach South Carolina 29572 Recruiting
Sarah Cannon Research Institute - Pharmacy Nashville Tennessee 37203 Recruiting
SCRI Oncology Partners Nashville Tennessee 37203 Recruiting
Texas Oncology - Austin Midtown Austin Texas 78705 Terminated
University of Texas Southwestern Medical Center - Simmons Cancer Center Dallas Texas 75390 Active, not recruiting
UT Southwestern Medical Center Dallas Texas 75390 Active, not recruiting
UT Southwestern University Hospital - William P. Clements, Jr Dallas Texas 75390 Active, not recruiting
UT Southwestern University Hospital - Zale Lipshy Dallas Texas 75390 Active, not recruiting
NEXT Dallas Irving Texas 75039 Recruiting
US Oncology Investigational Product Center (IPC) Irving Texas 75063 Terminated
US Oncology Investigational Products Center Irving Texas 75063 Terminated
NEXT Oncology San Antonio Texas 78229 Recruiting
Virginia Cancer Specialists, PC Fairfax Virginia 22031 Active, not recruiting
Olympic Medical Center Port Angeles Washington 98362 Active, not recruiting
Fred Hutchinson Cancer Center Alliance Peninsula Poulsbo Washington 98370 Active, not recruiting
Fred Hutchinson Cancer Center Seattle Washington 98109 Active, not recruiting
University of Washington Medical Center Seattle Washington 98109 Active, not recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03460977, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 23, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03460977 live on ClinicalTrials.gov.

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