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Western Canada · Lead-212 · GMP Manufacturing

Targeted Alpha Therapy
demands a supplier
within hours,
not days.

Pb-212 has a 10.6-hour half-life. A shipment from Ontario arrives with less than half its activity intact. Radia Theranostics is building Western Canada's first dedicated, GMP-controlled Pb-212 manufacturing platform to close that gap.

10.6
Hours
Pb-212 half-life
<6h
Target BC to US Pacific NW
>80%
Activity retention
GMP
CNSC · Health Canada
Illustrative depiction — Pb-212 half-life decay representation

Why Western Canada has no Pb-212 supply — and why that matters

Targeted alpha therapy (TAT) using Lead-212 is at the forefront of cancer treatment. But Pb-212's short half-life creates a logistics constraint that large centralized facilities are physically incapable of solving.

BC AB SK MB ON 50% lost here Radia BC (TBD) AtomVie Hamilton ON US Pacific NW Target <6h from BC Pb-212 activity decay over shipping distance
Illustrative depiction — simplified schematic, not to geographic scale
The Half-Life Constraint
With a 10.6-hour half-life, Pb-212 shipped from Ontario to BC loses more than 50% of its therapeutic activity in transit. Local manufacturing is not a preference — it is a physical necessity.
No GMP Pb-212 Facility in Western Canada
No CNSC/Health Canada-licensed GMP Pb-212 facility exists anywhere west of Ontario. Canadian clinical trials requiring Health Canada IND compliance cannot be supplied from US facilities.
Growing Clinical Demand
Pb-212-based targeted alpha therapy is advancing rapidly through late-stage clinical development, with NDA approval anticipated in the 2026–2027 timeframe. Growing clinical trial activity at western Canadian cancer centres and academic medical programmes is creating demand for a local GMP Pb-212 supply partner that does not yet exist.

Lead-212 and Targeted Alpha Therapy

Alpha particles deliver 50–100× the cell-killing energy of beta emitters, with a path length measured in microns — destroying tumour cells while sparing surrounding healthy tissue with unprecedented precision.

Alpha Particle Precision

Alpha particles travel only 40–80 µm in tissue — roughly 5–10 cell diameters. Targeted delivery means maximum cytotoxicity at the tumour site, minimal systemic dose.

In-Vivo Alpha Generator

Pb-212 acts as an in-vivo generator, delivering its daughter Bi-212 directly at the tumour site. This two-step radiobiology maximizes therapeutic efficacy without systemic alpha exposure during delivery.

Theranostic Pairing

Pb-212's SPECT-imageable decay product, Pb-203, enables a matched diagnostic-therapeutic pair — the same vector, same pharmacokinetics. True theranostics: image, then treat.

Pb-212 Decay Chain — Simplified
Ra
Radium-224
Source
Pb
Lead-212
t½ = 10.6h
Bi
Bismuth-212
In-vivo
Tl/Po
Stable
Daughters
Illustrative depiction — simplified decay chain. Ra-224 sourced from arm's-length third-party suppliers.

Western Canada's first GMP-controlled Pb-212 facility

A capital-efficient, purpose-built radioisotope manufacturing platform designed from the ground up for CNSC licensing and Health Canada GMP compliance — with a total build cost a fraction of centralized alternatives.

HOT CELL Pb-212 Generator Elution Station QC LAB Analytical Testing GMP Release CLEANROOM ISO Class 7 Radiolabeling OPERATIONS / RSO OVERSIGHT / SHIPPING & LOGISTICS COLD CHAIN DISPATCH
Illustrative facility layout depiction — not to scale
1
Generator Elution
Ra-224/Pb-212 generator operated in the shielded hot cell. Pb-212 is eluted on a scheduled production cycle tied to clinical delivery windows.
2
GMP Processing & Formulation
Pb-212 is processed, formulated and activity-assured within the ISO Class 7 cleanroom environment under full GMP documentation and SOP controls.
3
QC Testing & Batch Release
Each batch undergoes radionuclidic purity, chemical purity, sterility and activity testing before release. Health Canada DEL-compliant batch records maintained for every release.
4
Cold Chain Dispatch
Released units shipped via validated cold-chain protocols. Radia's BC facility location — currently in site selection — is being evaluated to ensure Western Canada and US Pacific NW clinical sites are reachable within the critical sub-6-hour delivery window.
Regulatory Pathway
CNSC Nuclear Substance Licence Year 1
Health Canada Drug Establishment Licence Month 18
First GMP Commercial Release Year 2

Why Western Canada needs this facility — and why none exists yet

No GMP-qualified Pb-212 manufacturing facility exists anywhere west of Ontario. The table below shows what Western Canadian clinical partners currently face when seeking Pb-212 supply — and what Radia is being built to provide.

USD $3.5B
2025–2026
Global radiopharmaceutical CDMO/manufacturing market
17%
CAGR
Targeted alpha therapy market growth to 2030
100×
Supply gap
Alpha isotope demand exceeds current global supply
$2.4B
AstraZeneca / Fusion
AstraZeneca's acquisition of Fusion Pharmaceuticals — most recent major Canadian radiopharmaceutical transaction
🔬
Facility Under Development

Radia Theranostics is currently in its facility build and qualification phase. First GMP commercial production is targeted following Health Canada Drug Establishment Licence approval, anticipated in Year 2 of operations. Clinical partners and trial sponsors are encouraged to engage now — anchor supply agreements entered during the build phase will directly inform production scheduling and capacity allocation.

Existing Options for Western Canadian Clinical Partners GMP BC Facility Health Canada Reg. Activity-Viable Western CA Delivery Canadian IND Supply
Radia Theranostics — In Development · BC — Site Selection Underway In Dev. In Dev. Planned ✓ Planned ✓
Orano Med ATLab (Indianapolis, USA) US only FDA only Trans-border Partial
AtomVie (Hamilton, ON) Ontario >50% activity lost in transit Not Pb-212
BWXT Medical (Ottawa, ON) Ontario >50% activity lost in transit Not Pb-212
Import (any US facility) Various

Table reflects current landscape as of mid-2026. Radia's planned capabilities are subject to regulatory approval and build timeline. "Canadian IND Supply" refers to Health Canada IND-compliant GMP Pb-212 isotope supply specifically.

A team built for this problem

Radia's founding team combines direct Pb-212 and alpha-isotope operating experience with GMP facility expertise, financial management, and dual CNSC/Health Canada regulatory knowledge — rare capabilities that converge in one place.

CF
Cameron Fraser
President & CEO · Director
Senior consultant in nuclear medicine and radiopharmaceuticals; research coordinator and industry outreach lead with deep relationships across the Ac-225 and At-211 research community. Leads Radia's technical coordination and commercial development.
JK
John Kos, CPA
Chief Financial Officer · Director
Chartered Professional Accountant with 25+ years of financial oversight for technical-construction and operating companies. Most recently provided financial oversight for a large cyclotron radiopharmaceutical project in BC.
WG
Warren Gray, M.Sc.
Production Line Development Lead
M.Sc. University of Southampton. International senior researcher overseeing build-out of the Pb-212 production line. Leads Radia's core isotope production research and development program in Year 1.
JL
James Labuef
Production Specialist · Founder
Nuclear Medicine Technologist (BCIT diploma). Specialist in GMP batch records, in-process controls, production SOPs, and aseptic technique. Senior hands-on lead for Pb-212 manufacturing operations.
DI
Daryl Inglis
Regulatory Affairs Officer
25+ years of technical project coordination across health and regulatory strategy. Leads Radia's dual CNSC/Health Canada regulatory pathway — a scarce and critical capability in BC life sciences.
TK
Tom Christoff, MBA
Director · Facility Installation
30+ years of senior technical engineering and construction experience. Will oversee facility installation, commissioning, testing and production once the BC site is confirmed.
Scientific & Clinical Advisory Board

Radia is supported by an internationally recognized scientific and clinical advisory board whose combined expertise spans the full value chain of targeted alpha therapy — from isotope production through to first-in-human clinical trials.

Collectively, the board brings direct experience in Pb-212, Ac-225, At-211, and Lu-177 isotope production; cyclotron and generator-based manufacturing at commercial scale; GMP radiopharmaceutical CMC development and regulatory submissions across Health Canada, FDA, and EMA frameworks; nuclear medicine clinical leadership at major North American and Asian academic medical centres; cold-chain logistics for short half-life isotopes across BC and North America; and principal investigator experience on first-in-human alpha therapy trials in PSMA-targeted and thyroid cancer indications. Their involvement directly informs Radia's production methodology, regulatory strategy, and clinical partner development.

Partner with Radia Theranostics

We are actively engaging clinical partners, trial sponsors, and institutional collaborators ahead of our first production release. If your programme requires a Western Canadian GMP Pb-212 supplier, we want to hear from you.

Clinical Trial Sponsors
Health Canada IND-compliant Pb-212 supply for Canadian trial arms. Discuss anchor supply agreements.
Cancer Centres & Hospitals
Western Canadian cancer centres and academic nuclear medicine programs seeking a regional GMP Pb-212 supply partner.
US Pacific Northwest Clinical Sites
Leading US Pacific Northwest academic medical centres and clinical trial sites — a BC-based facility is being sited to ensure delivery within the sub-6-hour activity window.
Investment Inquiries
For investor materials and investment information, please contact us directly.

This form is for partnership and supply inquiries. Investment-related materials are available on request and are subject to applicable securities requirements. All correspondence is treated as confidential.

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