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NCT06359379

Ropidoxuridine as a Radiosensitizer in Newly Diagnosed IDH-Wildtype Glioblastoma With Unmethylated MGMT Promoter

Terminated Phase 2 Last updated 18 December 2025
What this trial tests

Phase 2 trial testing Ropidoxuridine in Glioblastoma, IDH-wildtype in 30 participants. Terminated before completion.

Timeline
2 September 2024
Primary endpoint
1 December 2025
1 December 2025

Quick facts

Lead sponsorShuttle Pharmaceuticals, Inc.
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment30
Start date2 September 2024
Primary completion1 December 2025
Estimated completion1 December 2025
Sites6 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Shuttle Pharmaceuticals, Inc.

Who can join

18 and older, any sex, with Glioblastoma, IDH-wildtype. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomized, open-label, phase 2 study evaluating the safety and efficacy of oral ropidoxuridine as a radiation-sensitizing agent in patients with newly diagnosed wild-type isocitrate dehydrogenase glioblastoma with an unmethylated O6-methylguanine-DNA methyltransferase promoter, undergoing standard 60 Gy radiotherapy.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Clinical translation and landscape of stimuli-responsive nanomedicines and microscale therapeutics.
    Kobzev D, Kulyk O, Barmin RA, Tatarets A, et al · · 2026 · PMID 42210822 · DOI 10.1039/d6cs00165c
  2. Advancing cancer radiotherapy: Harnessing radiosensitizers and nanotechnology for enhanced tumor control.
    Shiridokht F, Kehtari P, Eskandani M, Farajollahi A, et al · · 2025 · PMID 41189671 · DOI 10.1016/j.ijpx.2025.100419

Verify or expand the search:

Other trials of Ropidoxuridine

Trials testing the same drug.

Other recruiting trials for Glioblastoma, IDH-wildtype

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06359379.

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