ClinicalTrials.gov record
Terminated Phase 1 Interventional

(VELA) Study of BLU-222 in Advanced Solid Tumors

ClinicalTrials.gov ID: NCT05252416

Public ClinicalTrials.gov record NCT05252416. 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 19, 2026, 11:21 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 1/2 Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of BLU-222 as a Single Agent and in Combination Therapy for Patients With Advanced Solid Tumors

Study identification

NCT ID
NCT05252416
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Blueprint Medicines Corporation
Industry
Enrollment
50 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 6, 2022
Primary completion
Jul 3, 2025
Completion
Jul 3, 2025
Last update posted
Nov 27, 2025

2022 – 2025

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
16
Facility City State ZIP Site status
University of Arkansas for Medical Sciences Little Rock Arkansas 72205
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California 94158
Stanford Women's Cancer Center Stanford California 94305
Florida Cancer Specialists Sarasota Florida 34232
University of Chicago Medical Center Chicago Illinois 60637
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center (SKCCC) Baltimore Maryland 21287
Massachusetts General Hospital Boston Massachusetts 02114
Dana-Farber Cancer Institute Boston Massachusetts 02215
Henry Ford Health System Detroit Michigan 48202
Columbia University Herbert Irving Comprehensive Cancer Center New York New York 10032
Memorial Sloan Kettering Cancer Center New York New York 10065
Montefiore Medical Center New York New York 10461
UNC Hospitals at Chapel Hill - The University of North Carolina at Chapel Hill Chapel Hill North Carolina 27514
OU Health Stephenson Cancer Center Oklahoma City Oklahoma 73104
Hospital of the Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Vanderbilt Breast Center at One Hundred Oaks Nashville Tennessee 37204
MD Anderson Cancer Center Houston Texas 77030
University of Utah - Huntsman Cancer Institute - PPDS Salt Lake City Utah 84112
University of Virginia Comprehensive Cancer Center Charlottesville Virginia 22903

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05252416, 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 Nov 27, 2025 · Synced May 19, 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 protocol, eligibility criteria, and contact information for NCT05252416 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →