Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1 Interventional

PRT3789 Monotherapy and in Combo w/Docetaxel in Participants w/Advanced or Metastatic Solid Tumors w/SMARCA4 Mutation

ClinicalTrials.gov ID: NCT05639751

Public ClinicalTrials.gov record NCT05639751. 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 Oct 26, 2026, 9:34 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 1 Open-Label, Multi-Center, Safety and Efficacy Study of PRT3789 as Monotherapy and in Combination With Docetaxel in Participants With Advanced or Metastatic Solid Tumors With a SMARCA4 Mutation

Brief summary

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

This is a Phase 1 dose-escalation study of PRT3789, a SMARCA2 degrader, in participants with advanced or metastatic solid tumors with loss of SMARCA4 due to truncating mutation and/or deletion. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) of PRT3789 monotherapy and in combination with docetaxel, describe any dose limiting toxicities (DLTs), define the dosing schedule, and to determine the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) to be used in subsequent development of PRT3789.

Study identification

NCT ID
NCT05639751
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
135 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
May 2, 2023 (Actual)
Primary completion
Oct 1, 2025 (Actual)
Completion
Oct 1, 2025 (Actual)
Last update posted
Oct 16, 2025

2023 – 2025

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of California, Davis Comprehensive Cancer Center Sacramento California 95817 —
UCLA Hematology/Oncology - Santa Monica Santa Monica California 90404 —
Smilow Cancer Hospital Phase 1 Unit New Haven Connecticut 06511 —
AdventHealth Medical Group Oncology Research at Celebration Celebration Florida 34747 —
Mayo Clinic, Jacksonville Jacksonville Florida 32224 —
Winship Cancer Institute Atlanta Georgia 30322 —
Northwestern Memorial Hospital Chicago Illinois 60611 —
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21287 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Mayo Clinic, Rochester Rochester Minnesota 55905 —
Washington University School of Medicine - Siteman Cancer Center St Louis Missouri 63110 —
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health New York New York 10016 —
New York Presbyterian Hospital - Columbia University Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Cleveland Clinic Cleveland Ohio 44195 —
Providence Cancer Institute Franz Clinic Portland Oregon 97213 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —
NEXT Virginia Fairfax Virginia 22031 —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05639751, 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 Oct 16, 2025 · Synced Oct 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05639751 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →