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Temozolomide, With or Without WSD0922-FU, for the Treatment of EGFR-Mutant, IDH-Wildtype Glioblastoma

StatusSuspended
PhasePhase 2
Started2026-08-28
View on ClinicalTrials.gov ↗

Amendment history

2026-08-31
critical
Study Status, Contacts/Locations, IPDSharing v2
Recruitment suspended: Pending receipt of study drug from sponsor
Recruitment opened
Primary completion pushed: 2036-07-31 → 2036-08-31
Completion pushed: 2036-07-31 → 2036-08-31
Start dateestimated 2026-08-16→confirmed 2026-08-28
Study sitesdetails revised at 3 of 3 sites
2026-07-21
minor
Study Status v1
Re-verified, no change to tracked fields
2026-07-13
minor
Original filing
1,015 trials monitored
See 115 trials at risk
666 trials monitored
See 45 trials at risk
This phase II trial compares the effect of adding WSD0922-FU to temozolomide versus temozolomide alone in slowing disease progression in patients with Epidermal Growth Factor Receptor (EGFR)-mutant, IDH-wildtype glioblastoma. Temozolomide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid and may kill tumor cells and slow down or stop tumor growth. WSD0922-FU is a targeted treatment which blocks EGFR. It is able to get into the brain and spinal cord and help treat those types of tumors. Adding WSD0922-FU to the usual treatment with temozolomide may be more effective in slowing disease progression, compared to temozolomide alone, in patients with EGFR-mutant, IDH-wildtype glioblastoma.
Trial Details
NCT Number NCT07708961
Lead Sponsor Mayo Clinic
Conditions Glioblastoma, IDH-Wildtype
Enrollment 60 participants
Start Date 2026-08-28
Primary Completion 2036-08-31 (estimated)
Study Completion 2036-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-09-23