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Completed Phase 1 Interventional

A Study of PRT543 in Participants With Advanced Solid Tumors and Hematologic Malignancies

ClinicalTrials.gov ID: NCT03886831

Public ClinicalTrials.gov record NCT03886831. 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 May 11, 2026, 4:33 PM 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, Multicenter, Dose Escalation, Dose Expansion Study of PRT543 in Patients With Advanced Solid Tumors and Hematologic Malignancies

Study identification

NCT ID
NCT03886831
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Prelude Therapeutics
Industry
Enrollment
232 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
Feb 10, 2019
Primary completion
Nov 15, 2022
Completion
Nov 15, 2022
Last update posted
Mar 27, 2023

2019 – 2022

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Banner MD Anderson Cancer Center Gilbert Arizona 85234
UCSF Precision Cancer Medicine Building San Francisco California 94158
Christiana Care Health Services, Christiana Hospital Newark Delaware 19718
Florida Cancer Specialists Lake Mary Florida 32746
Florida Cancer Specialist Sarasota Florida 34232
Moffitt Cancer Center Tampa Florida 33612
Georgia Cancer Center at Augusta University Augusta Georgia 30912
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Norton Cancer Institute, St. Matthews Campus Louisville Kentucky 40207
Ochsner Clinic Foundation New Orleans Louisiana 70121
Dana Farber Cancer Institute Boston Massachusetts 02215
University of Michigan Ann Arbor Michigan 48109
Atlantic Health System / Morristown Medical Center Morristown New Jersey 07962
Memorial Sloan Kettering Cancer Center New York New York 10065
Montefiore Medical Center The Bronx New York 10467
Levine Cancer Institute Charlotte North Carolina 28204
The Ohio State University and Wexner Medical Center Columbus Ohio 43210
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232
PLLC Nashville Tennessee 37203
The University of Texas MD Anderson Cancer Center Houston Texas 77030-4009
MD Anderson Cancer Center Houston Texas 77030
Seattle Cancer Care Alliance Seattle Washington 98109

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03886831, 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 Mar 27, 2023 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03886831 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →