Perspective Therapeutics Updates Interim Results of 212PbVMT-alpha-NET Clinical Trial
Perspective Therapeutics announced updated interim results from its ongoing Phase 1/2a clinical trial of 212PbVMT-alpha-NET in patients with unresectable or metastatic somatostatin receptor type 2 expressing neuroendocrine tumors are being presented as a poster presentation at the 2026 ASCO Gastrointestinal Cancers Symposium, taking place January 8-10 in San Francisco, CA. Interim results with a data cut-off date of December 10, 2025 formed the basis of the ASCO-GI update. The presentation includes safety data from 56 patients across three dose cohorts who have received at least one treatment of 212PbVMT-alpha-NET, and efficacy analysis from two patients in Cohort 1 and 23 of the patients in Cohort 2. Results with a data cut-off date of September 12, 2025 were previously presented at the European Society for Medical Oncology Congress 2025 in October 2025. At ESMO, the Company reported safety data on 55 patients across three dose cohorts who had received at least one treatment of 212PbVMT-alpha-NET and interim efficacy data for two patients in Cohort 1 and 23 patients in Cohort 2.
Trade with 70% Backtested Accuracy
Analyst Views on CATX
About CATX
About the author

Oncolytics Biotech's Breakthroughs in Cancer Treatment
- Market Potential: The global oncology market is projected to reach $668 billion by 2034, positioning Oncolytics Biotech at the forefront of this rapid growth, particularly in the treatment of gastrointestinal cancers through innovative immunotherapy.
- Clinical Trial Progress: Oncolytics Biotech's pelareorep achieved a 33% response rate in colorectal cancer patients, significantly surpassing the 6-11% response rates typical of standard chemotherapy, indicating a potential shift in treatment paradigms.
- Management Team Upgrade: The company appointed two key executives, John McAdory and Yujun Wu, with extensive experience in complex late-stage clinical trials and biostatistics, respectively, which will provide robust support for Oncolytics' clinical trial execution.
- FDA Trial Design Approval: Oncolytics has secured FDA approval for its Phase 3 trial design for pancreatic cancer, making it the only immunotherapy registration trial currently planned for this notoriously difficult-to-treat disease, marking a significant advancement for the company.

Perspective Therapeutics Updates VMT-α-NET Trial Results, 39% Patient Response Rate Achieved
- Clinical Trial Progress: Perspective Therapeutics presented updated results for VMT-α-NET at the ASCO-GI conference, revealing a 39% objective response rate among 23 patients, indicating the therapy's potential in treating unresectable neuroendocrine tumors.
- Safety Analysis: Among 56 treated patients, no dose-limiting toxicities (DLTs) were reported, and only 21 patients (37.5%) experienced grade 3 or higher treatment-related adverse events, demonstrating the therapy's favorable tolerability profile, which may support future clinical applications.
- Future Research Plans: The company plans to submit additional clinical data to medical conferences in 2026 and engage with regulatory agencies to advance VMT-α-NET into registrational trials, further validating its clinical efficacy.
- Dose Optimization: With the assessment of the 6.0 mCi dose cohort, Perspective has been cleared to enroll more patients, reflecting the company's ongoing progress in clinical trials and confidence in the new therapy, which could enhance its competitive position in the market.






