Morgan Stanley 24th Annual Global Healthcare Conference
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Perspective Therapeutics (CATX) Morgan Stanley 24th Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Perspective Therapeutics Inc

Morgan Stanley 24th Annual Global Healthcare Conference summary

9 Nov, 2026

Industry landscape and innovation

  • Radiopharmaceuticals deliver targeted radiation as a drug, potentially limiting damage to healthy tissue and enabling combination with other oncology modalities.

  • Lead-212 was selected for its half-life and imaging capabilities; proprietary technology addresses historical supply and chelation challenges.

  • More than 400 lead-212 generators have shipped globally, over 150 patients have been treated, and first-in-human imaging was achieved in the past year.

  • Lead-203 theranostic pairing supports patient selection and dosimetry; regional facilities and stockpiling strategies support scalable supply.

Study rationale and design

  • [212Pb] VMT-α-NET targets SSTR2; alpha particles deliver high-LET radiation over a short tissue path length, causing complex DNA damage.

  • A Pb-specific chelator showed ~95% 212Bi retention versus ~64% with DOTA, supporting lower redistribution of alpha-emitting 212Bi.

  • Phase 1/2a data included 68 PRRT-naïve patients with progressive, unresectable or metastatic NET after ≥1 systemic therapy; cutoff was Sep. 10, 2026.

  • Cohort 2 received 5.0 mCi × 4 (n=46); Cohort 3 received 6.0 mCi × 4 (n=20), with preliminary data; Cohort 4 frontloading at 6/5/5/4 mCi is enrolling.

Safety

  • 56/68 patients (82%) received all four planned doses; 67/68 (98.5%) had ≥1 TEAE, mostly Grade 1–2, and 20/68 (29.4%) had Grade 3 TEAEs.

  • No Grade 4/5 TEAEs, treatment-related SAEs, AE-related discontinuations within the defined TEAE window, or DLTs in DLT-evaluable patients.

  • Grade 3 hematologic TEAEs occurred in 5/68 (7.4%); no dysphagia or MDS was reported to date.

  • Two Grade 3 renal events occurred during follow-up: one possibly treatment-related AKI 756 days after last dose remained ongoing; another at 255 days was unlikely related and resolved.

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