Please wait

Slide 1

Redefining Oncology Treatment with Next-Generation Radiopharmaceuticals


Slide 2

 


Slide 3

Engineering the Alpha Advantage in Targeted Oncology


Slide 4

Unlocking New Treatment Options Across Solid Tumors:


Slide 5

Optimizing the Entire System


Slide 6

Rapidly Advancing Best-in-Class Next Generation Radiopharmaceuticals


Slide 7

Optimizing Structural Chemistry:


Slide 8

Choosing The Right Isotope


Slide 9

Not All ²¹²Pb Programs Are Created Equal


Slide 10

 


Slide 11

Advancing a Theranostic Approach:


Slide 12

Solid Tumors are an Attractive Market for Radiopharmaceuticals


Slide 13

Expanding the Addressable Market


Slide 14

Direct-to-Hospital Delivery through Integrated Isotope Production


Slide 15

Daily Production at Regional Sites Ensures Supply of Ready-to-Administer Product


Slide 16

Reaching the Largest Addressable Market with Regional Manufacturing


Slide 17

Advancing a Diverse 212Pb-Based Oncology Portfolio


Slide 18

SSTR2+ Neuroendocrine Tumors is a Large, Growing Market with Significant Unmet Need


Slide 19

VMT-⍺-NET: Potential First-in-Class 212Pb-Radioligand Therapy Targeting SSTR2


Slide 20

Ongoing Phase 1/2a to Establish Broad Therapeutic Window for VMT-⍺-NET in NETs


Slide 21

VMT-⍺-NET: Baseline Patient Characteristics in ASCO 2026 Data Analysis


Slide 22

Patient Exposure and Follow-up with [212Pb]VMT-α-NET in ASCO 2026 Data Analysis


Slide 23

VMT-α-NET Best Response Deepens Over Time


Slide 24

VMT-α-NET Responses Deepen Over Time


Slide 25

VMT-⍺-NET: Durable Disease Control Across All Doses


Slide 26

Spider Plot of Tumor Change Over Time by Patient


Slide 27

Best-in-class Safety Profile1


Slide 28

Blood Creatinine During Follow-up for All Patients Treated (n=68)


Slide 29

VMT-α-NET’s Compelling Profile Supports Potential Registration Study at Current Dose Level


Slide 30

Checkpoint Inhibitors Transformed Care of Melanoma but Leave Many Patients Behind


Slide 31

VMT01: Potential First-in-Class 212Pb Therapy Targeting MC1R for Melanoma


Slide 32

Ongoing Phase 1/2a Open-Label Trial For VMT01 in Melanoma


Slide 33

Preliminary Anti-tumor Activity Observed at 3.0 mCi Dose of VMT01


Slide 34

Treatment Emergent Adverse Events (All Grades, Occurring in ≥ 10% of Patients)


Slide 35

VMT01 is Well-tolerated with Initial Anti-tumor Activity Supporting Further Development


Slide 36

FAP-ɑ is an Attractive Cancer Target with Broad Solid Tumor Potential


Slide 37

PSV359: Potential First-in-Class 212Pb Therapy Targeting FAP-ɑ for Solid Tumors


Slide 38

Ongoing Open-label Phase 1/2a Trial For PSV359 in Advanced Solid Tumors


Slide 39

PSV359 has Improved Tumor Retention, Highlighting its Potential as a Therapeutic Agent


Slide 40

Strong IP Portfolio Covering All Aspects of Radiopharmaceutical Value Chain


Slide 41

 


Slide 42

A Decade of Deliberate, End-to-End Engineering


Slide 43

Built Over a Decade:


Slide 44

 


Slide 45

Abbreviations


Slide 46

APPENDIX


Slide 47

 


Slide 48

NETs Trials


Slide 49

Patient with Confirmed PR After [212Pb]VMT-α-NET Treatment


Slide 50

Refractory Metastatic Melanoma Trials


Slide 51

ICI Combo Rationale: Strong Synergy with [212Pb]VMT01 in Melanoma


Slide 52

Metastatic Melanoma: Confirmed Partial Response after 2 Cycles of [212Pb]VMT01


Slide 53

Perspective’s CCK2R81 in Medullary Thyroid Cancer Compared to FDG and Fluorodopa


Slide 54

 


Slide 55

 


Slide 56

Construct designed for better clinical outcome


Slide 57

212Pb Uniquely Suited for Combination with Immune Check Point Inhibitors


Slide 58

Kinetics Matter: 212Pb Hits Hard and Fast for Strong Activity with Less Systemic Exposure


Slide 59

 


Slide 60