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PLUS THERAPEUTICS, INC.

PSTV
$27MMicro Cap

Next catalyst

No upcoming catalyst in our data

No upcoming FDA decision, filing or trial readout is on file for PSTV. That does not mean none is planned.

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Track PLUS THERAPEUTICS (PSTV) and we email you when an FDA date moves, 7 days and 1 day before the decision when the exact day is known, and when it is announced. Free account, no card.

Catalyst Timeline

0 upcoming, 0 past

No catalysts found.

Market Overview

Stock performance and key metrics

NASDAQSurgical & Medical Instruments & ApparatusBiotechnology / Pharmaceuticals๐Ÿ‡บ๐Ÿ‡ธNorth AmericaHOUSTON28 employees

Plus Therapeutics, Inc. is a clinical-stage pharmaceutical company headquartered in Houston, Texas, that develops targeted radiotherapeutics and diagnostic services for brain and central nervous system (CNS) cancers. The companyโ€™s lead therapeutic candidate, marketed as REYOBIQโ„ข (rhenium Re-186 obisbemeda), is an investigational liposomal radiopharmaceutical under clinical evaluation for recurrent glioblastoma, leptomeningeal metastases, and certain pediatric brain cancers. Plus Therapeutics also commercialized a molecular diagnostic service, CNSideยฎ.

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Drug Pipeline

Frequently asked questions

What is in PLUS THERAPEUTICS, INC.'s drug pipeline?โ†’

CatalystAlert tracks 1 drug candidate in PLUS THERAPEUTICS, INC.'s (PSTV) pipeline across Phase 2. Its lead program is Rhenium Liposome Treatment (Phase 2). Each drug's phase, indication and upcoming catalysts are listed on this page.

When is PLUS THERAPEUTICS, INC.'s next FDA catalyst?โ†’

CatalystAlert tracks every upcoming catalyst for PLUS THERAPEUTICS, INC. (PSTV) โ€” PDUFA decision dates, Phase 1/2/3 trial readouts, FDA advisory committee meetings and NDA/BLA filings โ€” each confidence-rated as confirmed, estimated or AI-detected.

How do I track PSTV biotech catalysts?โ†’

Add PSTV to your CatalystAlert watchlist for alerts ahead of each catalyst, and follow PLUS THERAPEUTICS, INC.'s live catalyst calendar, drug pipeline and clinical-trial timeline on this page โ€” sourced from ClinicalTrials.gov, FDA and SEC filings.

Data is aggregated from public sources (FDA, SEC, ClinicalTrials.gov). While we strive for accuracy, information may be incomplete, delayed, or contain errors. Terms apply