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

PHASE1RecruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

December 12, 2024

Primary Completion Date

March 1, 2028

Study Completion Date

March 1, 2028

Conditions
Glioma
Interventions
DRUG

Retreatment Rhenium Liposome

At the time of stereotactic biopsy a catheter will be placed within the tumor using stereotactic guidance. Once the patient has adequately recovered from the procedure as determined by the neurosurgeon, 186RNL will be infused through the CED catheter at the predetermined dose. Spectroscopic imaging will then be obtained at predefined time points to visualize the distribution of the 186RNL as well as calculated the actual dose retained within the tumor. Patients will be monitored longitudinally for evidence of toxicity and response by MRI.

Trial Locations (1)

78229

RECRUITING

The Cancer Therapy and Research Center at UTHSCSA, San Antonio

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Plus Therapeutics

INDUSTRY