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NCT05267106 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Incyte Corporation.

Terminated
Registry status
Phase 2
Development phase
83
Enrollment target

NCT05267106 is a Phase 2 study that was terminated before completion, run by Incyte Corporation. The registered enrollment target is 83 participants.

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The verdict

NCT05267106, a Phase 2 study, was terminated before completion, sponsored by Incyte Corporation.

TERMINATED
Registry status
Phase 2
Development phase
83 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Pemigatinib

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2022-05-20
Est. Completion 2024-12-17
Phase Phase 2

Sponsor

Incyte Corporation

239 total trials

What the Registry Record Tells You About NCT05267106

The ClinicalTrials.gov registry entry for NCT05267106 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 83 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Pemigatinib is the first listed.

NCT05267106 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05267106 about?

NCT05267106 is a clinical study titled "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". 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, ...

What is the current status of trial NCT05267106?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 83 participants. The study started on 2022-05-20. Estimated completion is 2024-12-17.

What interventions are being tested in trial NCT05267106?

The interventions under investigation include: Pemigatinib (DRUG).

Who is sponsoring clinical trial NCT05267106?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.