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NCT06359379
Ropidoxuridine as a Radiosensitizer in Newly Diagnosed IDH-Wildtype Glioblastoma With Unmethylated MGMT Promoter
Phase 2 trial testing Ropidoxuridine in Glioblastoma, IDH-wildtype in 30 participants. Terminated before completion.
1 December 2025
Quick facts
| Lead sponsor | Shuttle Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 2 September 2024 |
| Primary completion | 1 December 2025 |
| Estimated completion | 1 December 2025 |
| Sites | 6 locations across United States |
Drugs / interventions tested
- Ropidoxuridine — full drug profile →
Conditions studied
- Glioblastoma, IDH-wildtype — all drugs for Glioblastoma, IDH-wildtype →
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):
-
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 -
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:
- PubMed search for NCT06359379
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Ropidoxuridine
Trials testing the same drug.
- NCT04406857 — Testing the Addition of a Radiation Sensitizing Drug, IPdR, to the Usual Chemotherapy Treatment (Capecitabine) During Ra · Phase 1 · terminated
- NCT02993146 — Ropidoxuridine and Whole Brain Radiation Therapy in Treating Patients With Brain Metastases · Phase 1 · active not recruiting
- NCT02381561 — Ropidoxuridine in Treating Patients With Advanced Gastrointestinal Cancer Undergoing Radiation Therapy · Phase 1 · active not recruiting
Other recruiting trials for Glioblastoma, IDH-wildtype
Currently open trials in the same condition.
- NCT06419946 — Lomustine in Addition to Standard of Care in Patients With MGMT Methylated Glioblastoma · Phase 3 · recruiting
- NCT06327451 — Evaluate the Efficacy and Safety of Atorvastatin Combined With Temozolomide in the Treatment of Glioblastoma · Phase 2 · recruiting
- NCT06418113 — Neoadjuvant Radio-chemotherapy Safety Pilot Study in Patients With Glioblastoma · Phase 1 · recruiting
- NCT05941234 — Stem Cell Analysis, Omics (Including Immunomics) and Artificial Intelligence in Glioblastoma · NA · recruiting
- NCT05929495 — Phase 2, Open-label, Single-arm Study on the Use of Metformin as Adjunctive Therapy in High-grade Glioma · Phase 2 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06359379 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Shuttle Pharmaceuticals, Inc.
- Last refreshed: 18 December 2025
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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