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Terminated Phase 2 Interventional Results available

Study to Evaluate the Efficacy and Safety of Pemigatinib in Participants With Previously Treated Glioblastoma or Other Primary Central Nervous System Tumors Harboring Activating FGFR1-3 Alterations

ClinicalTrials.gov ID: NCT05267106

Public ClinicalTrials.gov record NCT05267106. 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 21, 2026, 2:13 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 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Pemigatinib in Participants With Previously Treated Glioblastoma or Other Primary Central Nervous System Tumors Harboring Activating FGFR1-3 Alterations (FIGHT-209)

Brief summary

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

This is an open-label, monotherapy study of pemigatinib in participants with recurrent glioblastoma (GBM) or other recurrent gliomas, circumscribed astrocytic gliomas, and glioneuronal and neuronal tumors with an activating FGFR1-3 mutation or fusion/rearrangement. This study consists of 2 cohorts, Cohorts A, and B, and will enroll approximately 82 participants into each cohort. Participants will receive pemigatinib 13.5 mg QD on a 2-week on-therapy and 1-week off-therapy schedule as long as they are receiving benefit and have not met any criteria for study withdrawal.

Study identification

NCT ID
NCT05267106
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
83 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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 20, 2022 (Actual)
Primary completion
Dec 17, 2024 (Actual)
Completion
Dec 17, 2024 (Actual)
Last update posted
Dec 30, 2025

2022 – 2024

United States locations

U.S. sites
32
U.S. states
15
U.S. cities
31
Facility City State ZIP Site status
Valkyrie Clinical Trials Beverly Hills California 90211 —
City of Hope National Medical Center Duarte California 91010 —
Providence Medical Foundation Fullerton California 92835 —
Usc Norris Comprehensive Cancer Center Los Angeles California 90033 —
Stanford Neuroscience Health Center Sacramento California 94304 —
Sharp Memorial Hospital San Diego California 92123 —
University of California San Francisco San Francisco California 94143 —
Providence St Joseph Hospital Orange Center For Cancer Prevention and Treatment Santa Monica California 90404 —
Yale Cancer Center New Haven Connecticut 06510-3220 —
Baptist Md Anderson Cancer Center Jacksonville Florida 32207 —
Miami Cancer Institute Miami Florida 33176 —
Orlando Health Cancer Institute Downtown Orlando Orlando Florida 32806 —
H. Lee Moffitt Cancer Center and Research Institute Hospital Tampa Florida 33612 —
University of Illinois Hospital & Health Sciences System Chicago Illinois 60612 —
University of Iowa Hospital and Clinics Iowa City Iowa 52242 —
University Medical Center New Orleans New Orleans Louisiana 70112 —
University of Minnesota Health Clinics and Surgery Center Minneapolis Minnesota 55455 —
Northwell Health Lake Success New York 11042 —
Columbia University Irving Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
East Carolina University Greenville North Carolina 27834 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
UC Health At Cincinnati Va Medical Center Cincinnati Ohio 45229 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
University of Pennsylvania Hospital Philadelphia Pennsylvania 19104 —
University of Pittsburgh Medical Center Health System Pittsburgh Pennsylvania 15232 —
Tennessee Oncology Chattanooga Tennessee 37403 —
Tennessee Oncology Nashville Tennessee 37203 —
Baylor University Medical Center Dallas Texas 75246 —
Houston Methodist Hospital Houston Texas 77030 —
Huntsman Cancer Institute Salt Lake City Utah 84112 —
Fred Hutchinson Cancer Research Center 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05267106, 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 Dec 30, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05267106 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →