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Safety & Efficacy/Tolerability of Rhenium-186 NanoLiposomes (186RNL) for Patients Who Received a Prior 186RNL Treatment

StatusRecruiting
PhasePhase 1
SponsorCerenome
Started2024-12-12
View on ClinicalTrials.gov ↗

Amendment history

2025-03-25
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v4
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-03-01→confirmed 2024-12-12
Study sites0→1
2024-07-24
minor
Study Status, Contacts/Locations v3
Primary completion date2025-01-31→2028-03-01
Completion date2025-01-31→2028-03-01
Start date2023-01-02→2025-03-01
2022-12-22
minor
Study Status v2
Start date2022-12-10→2023-01-02
2022-12-07
minor
Study Status, Contacts/Locations v1
Start date2022-08-30→2022-12-10
2022-07-12
minor
Original filing
5 trials monitored
See 1 trial at risk
666 trials monitored
See 38 trials at risk
This is an open-label, multicenter, Phase 1 study to establish the safety and efficacy/tolerability of a single dose of 186RNL by the intraventricular route (via intraventricular catheter) for recurrence glioma in patients who received a prior treatment of 186RNL.
Trial Details
NCT Number NCT05460507
Lead Sponsor Cerenome
Conditions Glioma
Enrollment 40 participants
Start Date 2024-12-12
Primary Completion 2028-03-01 (estimated)
Study Completion 2028-03-01 (estimated)
Updated on ClinicalTrials.gov 2025-03-30