Welcome to our dedicated page for Plus Therapeutics news (Ticker: PSTV), a resource for investors and traders seeking the latest updates and insights on Plus Therapeutics stock.
Plus Therapeutics, Inc. (NASDAQ: PSTV) generates a steady flow of news as a clinical-stage pharmaceutical and healthcare company focused on targeted radiotherapeutics and precision diagnostics for central nervous system (CNS) cancers. Headquartered in Houston, Texas, the company regularly reports on its clinical trial progress, regulatory interactions, capital markets activity, and expansion of its CNSide Diagnostics subsidiary.
News about Plus Therapeutics often highlights developments related to REYOBIQ™ (rhenium Re186 obisbemeda), its lead investigational radiotherapy for recurrent glioblastoma, leptomeningeal metastases, and pediatric brain cancers. Updates include clinical data presentations at major oncology meetings, safety and efficacy findings from the ReSPECT-GBM and ReSPECT-LM trials, and discussions with the U.S. Food and Drug Administration (FDA) on pivotal trial design and potential accelerated approval pathways.
Another key news theme is the company’s CNSide Diagnostics, LLC subsidiary and the CNSide® CSF Assay Platform. Press releases describe new state laboratory licenses, national coverage agreements with major payors, and real-world utilization metrics for the CNSide cerebrospinal fluid Tumor Cell Enumeration test used in managing leptomeningeal metastases.
Investors following PSTV can also expect announcements on financing and listing matters, such as public offerings of common stock and warrants, purchase agreements with institutional investors, and updates on Nasdaq listing compliance related to minimum bid price and equity standards. Corporate governance items, including proxy statements and stockholder meeting results, appear in both news and SEC filings.
This news page aggregates these updates so readers can track Plus Therapeutics’ clinical milestones, diagnostic platform expansion, regulatory communications, and capital markets events in one place. For those researching PSTV, it provides context on how the company is advancing its CNS cancer programs and managing its public company obligations over time.
Plus Therapeutics has reported promising data from its ReSPECT™ Phase 1 trial for Rhenium-186 NanoLiposome (186RNL) in treating recurrent glioblastoma. The investigational drug demonstrated good tolerance at high radiation doses, outperforming standard therapies. Key findings include a mean dose of 392 Gy delivered safely, with no serious adverse events noted. The company plans to expand research into pediatric brain tumors, starting a Phase 1 study by mid-2022. The overall response rate will be a primary endpoint in the upcoming trials.
Plus Therapeutics (PSTV) recently presented promising preclinical data supporting its FDA IND application for Rhenium-186 Nanoliposome (186RNL) targeted radiotherapy aimed at treating leptomeningeal metastases (LM). The data, showcased at the Society for Neuro-Oncology's conference, indicated minimal toxicity and significant efficacy in animal models. Plans for a Phase 1 dose escalation clinical trial with patient accrual expected in Q4 2021 were also outlined. The trial will evaluate the treatment's safety and efficacy in patients previously treated for breast or non-small cell lung cancer with LM.
Plus Therapeutics, Inc. (Nasdaq: PSTV) announced it will present data on Rhenium-186 NanoLiposome from its Phase 1 ReSPECT™ trial for recurrent glioblastoma at the American Association of Neurological Surgeons 2021 Annual Scientific Meeting, held virtually from August 21-25, 2021. The presentation titled "A two-part, Phase 1 study of Rhenium-186 NanoLiposome" will be made available on-demand beginning August 21. Lead presenter Michael G. DeCuypere, MD, PhD, will provide insights on the study's findings, which aim to enhance treatment for rare cancers.
AUSTIN, Texas, Aug. 11, 2021 – Plus Therapeutics (Nasdaq: PSTV) announced data presentation at the Third Annual Conference on Brain Metastases by the Society for Neuro-Oncology. The studies evaluate Rhenium-186 Nanoliposome (186RNL) for leptomeningeal metastases treatment. Andrew J. Brenner, M.D., will present findings from the ongoing ReSPECT-GBM Phase 1 trial and a preclinical study showing that 186RNL is well tolerated and improves survival in animal models. The conference runs from August 19-20, 2021, with data available to attendees.
Plus Therapeutics (PSTV) announced that CEO Marc H. Hedrick M.D. will provide a company overview at the Canaccord Genuity 41st Annual Growth Conference on August 12, 2021, at 4:30 p.m. ET. The presentation will focus on Plus Therapeutics' innovative radiotherapeutics targeting rare cancers, utilizing a unique nanotechnology platform. Investors wishing to schedule meetings can contact the conference coordinator. A webcast will be available in the Investor Relations section of the Plus Therapeutics website.
Plus Therapeutics, Inc. (PSTV) has entered a ten-year exclusivity agreement with ABX Advanced Biochemical Compounds GmbH for the supply of a key component in the manufacturing of Rhenium-186 NanoLiposome (186RNL), their lead radiotherapeutic. This partnership will ensure a high purity precursor produced under cGMP, meeting FDA standards. The agreement not only strengthens Plus Therapeutics’ supply chain but also secures long-term market protection around their RNL portfolio, which is key in treating recurrent glioblastoma and other rare cancers.
Plus Therapeutics, Inc. (Nasdaq: PSTV) announced its financial results for Q2 2021, reporting a net loss of $2.8 million, or $(0.25) per share. The company's cash balance increased to $17.2 million, up from $8.3 million at year-end 2020. Highlights include ongoing clinical trials for the Rhenium-186 NanoLiposome (186RNL) targeting recurrent glioblastoma, with 22 patients treated and an eighth cohort underway. The company plans to submit IND applications for Leptomeningeal Metastases and Pediatric Brain Cancer trials by year-end 2021. A conference call will discuss these results at 5:00 PM ET today.
Plus Therapeutics, Inc. (PSTV) announced the successful treatment of the first patient in the eighth cohort of their Phase 1 ReSPECT™-GBM clinical trial for recurrent glioblastoma. This cohort features a 40% increase in treatment volume and radioactivity compared to previous cohorts. To date, 22 patients have been treated across eight cohorts with no dose-limiting toxicities reported. The trial is progressing as scheduled, and an update is expected in Q4 2021.
Plus Therapeutics (PSTV) announced it will report its second quarter 2021 financial results on July 22, 2021, after market close. A conference call and webcast to discuss the results and provide a corporate update will follow at 5:00 p.m. ET. Plus Therapeutics focuses on developing targeted radiotherapeutics for rare cancers, utilizing a nanotechnology platform for drug delivery and formulation. This innovative approach aims to enhance the safety and efficacy of treatments for difficult-to-treat cancers.
Plus Therapeutics (PSTV) announced a significant step forward in their ReSPECT™ trial for Rhenium NanoLiposome (RNL™) in treating recurrent glioblastoma (GBM). The Data and Safety Monitoring Board has approved advancing to the eighth cohort, which will feature a 40% increase in total radioactivity, escalating the infused dose to 31.2 millicuries. RNL™ has demonstrated a favorable safety profile with no dose-limiting toxicities observed in the first seven cohorts, treating 21 patients. The trial is supported by the NIH/National Cancer Institute at three U.S. sites.