Oral gallium maltolate trial for recurrent glioblastoma
Summary
The National Institutes of Health registered ClinicalTrials.gov study NCT07515924, a Phase 1 interventional trial evaluating oral gallium maltolate in patients with recurrent glioblastoma. The trial will assess safety, tolerability, and maximum tolerated dose in an estimated patient cohort. Gallium maltolate is an investigational gallium-based compound under study for potential anticancer activity against glioblastoma.
What changed
ClinicalTrials.gov has published a new trial registration for NCT07515924, an early-phase study of oral gallium maltolate in recurrent glioblastoma. The registry entry documents the trial's objectives, design, eligibility criteria, and investigator information. No regulatory approvals, safety alerts, or enforcement actions are associated with this registration.\n\nSponsors and investigators conducting drug trials for glioblastoma should note this trial as part of the competitive landscape for CNS oncology therapeutics. Patients and advocacy organizations may find this trial relevant for treatment options. The registration provides no new compliance obligations but signals continued interest in gallium-based compounds for brain cancer.
What to do next
- Monitor ClinicalTrials.gov for updates to recruitment status, enrollment numbers, and preliminary results
- Ensure institutional review board (IRB) oversight if affiliated with the sponsoring institution
- Review any future IND filings or FDA communications related to gallium maltolate development
Archived snapshot
Apr 7, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
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