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Plus Therapeutics (PSTV) investor relations material
Plus Therapeutics Investor update summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Corporate rebranding and strategic direction
Announced rebranding to Cerenome with new Nasdaq ticker CNSY effective August 3, 2026, reflecting a broader focus on integrated CNS oncology, including therapeutics, diagnostics, and proprietary data.
The new name aligns with the company's evolution beyond radiotherapeutics, emphasizing integration of therapy, diagnostics, and data for CNS cancers.
Operational structure will maintain distinct business units for therapeutics, diagnostics, and data analytics/AI, leveraging native AI for efficiency and commercial opportunity.
Launch of new corporate website and coordinated investor communications planned for August, with full brand rollout at SNO/ASCO meeting.
Therapeutics division and clinical progress
REYOBIQ (rhenium-186 obisbemeda) advancing in multiple CNS cancer indications, with 2026 objectives on track: dose optimization in ReSPECT-LM phase II, enrollment in ReSPECT-GBM phase II, manufacturing scale-up, and initiation of ReSPECT-PBC pediatric trial.
Interim data for ReSPECT-LM expected in H2 2026; trial design incorporates FDA feedback, including randomization and patient-reported outcomes.
ReSPECT-GBM phase II has enrolled 31 of 34 subjects, with data expected Q4 2026; pivotal trial decision will be data-dependent.
Manufacturing and supply chain improvements are on schedule, supporting both clinical and early commercial needs, with key FDA recommendations implemented.
RESPECT-PBC pediatric trial approved by DoD and IRB, with first dosing expected Q3 2026.
Diagnostics (CNSide) division update
CNSide platform expanded payer coverage from 67 million to 126 million covered lives in 2026, with recent agreements from Highmark, Blue Shield of California, and Elevance Health.
Four 2026 goals on track: expanding U.S. payer coverage to 150M+ lives, securing Medicare pathway, achieving 1,250 annualized test order run rate, and launching additional CSF tumor characterization assays.
Medicare enrollment and PLA code effective July 1, enabling direct claims submission; MAC determinations and fee schedule pricing are next milestones.
Test order volume grew 64% Q1-Q2, with June setting a record; 232 tests performed YTD and physician adoption tripled since January.
Plans to launch three new CSF specimen assays in Q3 2026 to enhance clinical data and value, with incremental reimbursement expected.
- $15M raise funds pivotal trials, CNSide scale-up, and 2026 commercial expansion.PSTV
Business update9 Jul 2026 - $15M financing and clinical progress support CNSide's 2025 launch and CNS cancer milestones.PSTV
Q4 20248 Jul 2026 - Shelf registration allows flexible securities offerings; Canaccord Genuity LLC is distribution agent.PSTV
Registration filing5 Jun 2026 - At-the-market equity offering of up to $17.35M targets CNS cancer innovation, with dilution risk.PSTV
Registration filing2 Jun 2026 - 186RNL shows safety, efficacy, and immune activation in leptomeningeal metastases.PSTV
2026 AANS Annual Scientific Meeting presentation22 May 2026 - Net loss narrowed, cash and investments rose, and funding remains critical amid clinical and commercial progress.PSTV
Q1 202615 May 2026 - All proposals, including board election and stock plan amendment, were approved by shareholders.PSTV
AGM 202614 May 2026 - Key votes include director elections, auditor ratification, and executive pay approval.PSTV
Proxy filing31 Mar 2026 - Board seeks approval for director elections, auditor ratification, and expanded equity plan.PSTV
Proxy filing31 Mar 2026
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