Drugs / 186RNL

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07674693 Jul 2026 → Jul 2028 expected neoplastic meningitis NYU Langone Health Not yet recruiting No outcome recorded
Phase 1 NCT07061626 Sep 2025 → Mar 2027 expected ependymoma, malignant glioma Plus Therapeutics Not yet recruiting No outcome recorded
Phase 1 NCT07098806 Jul 2025 → Oct 2026 expected neoplastic meningitis Plus Therapeutics Recruiting No outcome recorded
Phase 1 NCT05460507 Dec 2024 → Mar 2028 expected glioma Plus Therapeutics Recruiting No outcome recorded
Phase 1 NCT05034497 Dec 2021 → Dec 2025 overdue neoplastic meningitis Plus Therapeutics Active not recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 24

DateIssuerRelease
2026-08-20 Plus Therapeutics Results Cerenome Highlights Presentations at the 2026 SNO/ASCO CNS Metastases Conference Demonstrating Progress in Both Therapeutics and Diagnostics Business Lines cerenome.com ↗
One presentation featured updated pharmacokinetic (PK), pharmacodynamic (PD), dosimetry, safety and activity data for REYOBIQ™ (rhenium-186 obisbemeda) in patients with leptomeningeal metastases (LM), including emerging safety data from the ongoing repeated-dosing program.
2026-05-08 Plus Therapeutics Results Plus Therapeutics Announces Oral Presentation Highlighting REYOBIQ™ Clinical and Translational Data Demonstrating Favorable Safety, Survival, and Emerging Immunomodulation in Leptomeningeal Metastases cerenome.com ↗
2026-04-08 Plus Therapeutics Regulatory Plus Therapeutics Granted U.S. FDA Orphan Drug Designation to REYOBIQ™ in Pediatric Malignant Gliomas cerenome.com ↗
Plus Therapeutics, Inc. (Nasdaq: PSTV ) (the “Company”), a clinical-stage pharmaceutical company developing targeted radiotherapeutics with advanced platform technologies for central nervous system (CNS) cancers, today announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to REYOBIQ™ (rhenium Re186 obisbemeda) for the treatment of pediatric malignant gliomas.
2025-12-04 Plus Therapeutics Results Plus Therapeutics Highlights Three REYOBIQ™ Clinical Data Presentations at 2025 WFNOS/SNO Annual Meeting cerenome.com ↗
Phase 1 ReSPECT-GBM showed promising improvements in overall survival
2025-08-18 Plus Therapeutics Results Plus Therapeutics Presents Positive ReSPECT-LM Clinical Trial Results of REYOBIQ™ in Leptomeningeal Metastases cerenome.com ↗
The data demonstrated treatment of leptomeningeal metastases (LM) with REYOBIQ is feasible, has a manageable safety profile, and shows a promising efficacy signal.
2025-06-25 Plus Therapeutics Regulatory Plus Therapeutics Announces FDA Clearance of its Investigational New Drug Application using REYOBIQ™ for the Treatment of Childhood Brain Cancer cerenome.com ↗
2025-05-14 Plus Therapeutics Results Plus Therapeutics’ REYOBIQ™ Shows Clinical Benefit and Safety in the ReSPECT-LM Clinical Trial for Patients with Leptomeningeal Metastases (LM) cerenome.com ↗
This newly presented data shows safety, clinical benefit and data supporting the underlying mechanism of action for REYOBIQ in patients with Leptomeningeal Metastases,
2025-04-15 Plus Therapeutics Results Plus Therapeutics Presents New Data Highlighting Clinical Benefit and Safety of REYOBIQ in the ReSPECT-LM Clinical Trial for Patients with Leptomeningeal Metastases cerenome.com ↗
Neuroimaging response data was available for 16 patients as of the data cutoff with five of those (31%) showing a partial response.
2025-03-20 Plus Therapeutics Regulatory Plus Therapeutics Introduces REYOBIQ™, FDA-Accepted Proprietary Name for Lead Drug Candidate cerenome.com ↗
2024-10-01 Plus Therapeutics Results Plus Therapeutics Reports ReSPECT-GBM Clinical Trial Update at the 2024 Congress of Neurological Surgeons Annual Meeting cerenome.com ↗
The data highlights the continued favorable safety profile and encouraging efficacy results of Rhenium ( 186 Re) Obisbemeda in a patient population with historically poor prognosis.
2023-06-29 Plus Therapeutics Results Plus Therapeutics Reports Positive Interim Updates from Two ReSPECT™ Clinical Trials at SNMMI Annual Meeting cerenome.com ↗
A single dose of rhenium ( 186 Re) obisbemeda was generally safe and well-tolerated, with no dose-limiting toxicities and minimal systemic radiation exposure.
2022-11-19 Plus Therapeutics Results Plus Therapeutics Provides Updates on ReSPECT™ Clinical Trials at the 27th Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology cerenome.com ↗
Targeted radiotherapy using rhenium ( 186 Re) obisbemeda in patients with GBM and LM has, thus far, been shown to be both feasible and safe across a range of dosages and a variety of delivery parameters.

All press releases naming this drug 43 releases

DateIssuerRelease

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as 186RNL “Rhenium (186Re) Obisbemeda (Rhenium-186 NanoLiposome, 186RNL), BMEDA-chelated-186rhenium encapsulated within liposomes, allows the 186Re to be directly delivered to the site of...” NCT07061626 ↗
4

“This Phase I clinical study evaluates a single dose of 186RNL (radionuclide clinical study drug) administered through a convection enhanced delivery catheter (CED catheter) in...” NCT05460507 ↗

NCT05034497 ↗

NCT07098806 ↗

NCT07674693 ↗

Known as REYOBIQ “Rhenium-186 NanoLiposome (186RNL, REYOBIQ)” NCT07674693 ↗
Known as Rhenium (186Re) Obisbemeda “Rhenium (186Re) Obisbemeda (Rhenium-186 NanoLiposome, 186RNL), BMEDA-chelated-186rhenium encapsulated within liposomes, allows the 186Re to be directly delivered to the site of...” NCT07061626 ↗
1

“Rhenium (186Re) Obisbemeda (Rhenium-186 NanoLiposome, 186RNL) Administered Via Intraventricular Catheter” NCT07098806 ↗

Known as Rhenium-186 NanoLiposome “Rhenium (186Re) Obisbemeda (Rhenium-186 NanoLiposome, 186RNL) Administered Via Intraventricular Catheter” NCT07098806 ↗
Modality Other / unclassified “186RNL (radionuclide clinical study drug)” NCT05034497 ↗
Route Other “via intraventricular catheter” NCT05034497 ↗