How the Model Works

Partner with Your Practice

We work with uro-oncologists, urology and oncology groups that have patients who may benefit from radioligand therapy.

Choose the Right Partnership Model

Together, we find a partnership model that works for both sides from a referral or service agreement to a joint venture, tailored to your practice and patient volume.

ParticleX Builds and Operates the Center

We build out, equip, and operate the radioligand therapy center, including the specialized infrastructure, clinical team, and treatment capabilities.

Your Patients Stay with Your Practice

You remain the patient’s primary oncologist, ParticleX provides the radioligand therapy and coordinates treatment with your clinical team.

Cleanroom specialist working with hot cell manipulator Specialist inside high-tech radiopharmaceutical cleanroom
Specialist operating pharmaceutical synthesis module

Our Vision

Radioligand therapy is becoming part of mainstream oncology and moving into earlier lines of treatment.

ParticleX is building a theranostics platform around this shift, starting with Lutetium-177 PSMA therapy for prostate cancer, and creating the clinical infrastructure for a much broader range of radiopharmaceutical therapies.

Our focus includes next-generation alpha therapies using Actinium-225, Lead-212 and Astatine-211, combined with targets such as PSMA, FAP, FAPI, HER2, GRPR and DLL3. These programs have the potential to extend radioligand therapy across prostate cancer and other solid tumors, making new radiopharmaceuticals and new cancer indications a core part of the ParticleX platform.

Lu-177 PSMA Moving to the Front of Care

2015
2022
2025
2026
2015

First Clinical Use

First clinical experience with Lu-177 PSMA-617 showed that PSMA-targeted radiation could reach metastatic prostate cancer and produce meaningful tumor and PSA responses.

2022

FDA Approval

Lu-177 PSMA received its first FDA approval for PSMA-positive mCRPC after AR pathway therapy and taxane chemotherapy.

2025

Before Chemotherapy

The FDA expanded Lu-177 PSMA to PSMA-positive mCRPC after ARPI therapy for patients appropriate to delay taxane chemotherapy, moving treatment earlier in the disease course.

2026

First line, alongside hormonal therapy

FDA approved Lu-177 PSMA with ARPI for PSMA-positive metastatic hormone-sensitive prostate cancer, bringing Lu-177 PSMA into use with hormonal therapy from the start of metastatic treatment.

Global Nuclear Medicine Network Global Nuclear Medicine Network

Our Experience

15+ years building businesses in nuclear medicine and radiopharmmaceuticals.

PETSCAN Network

2 cyclotron-radiopharmaceutical centers
5 nuclear medicine centers

Engineering Division

Design and development of nuclear medicine center and radiopharmaceutical production facilities

International Experties

Designed and built facilities in Europe

Participated in the development of the Nuclear Research and Technology Center in Bolivia

EUROPE
BOLIVIA

What We’ll Need From Partners

Tell us about your practice

Tell us about your practice and we’ll explore how radioligand therapy can fit your patient flow.

Discuss patient volume

We'll review your patient population and identify which patients are candidates for radioligand therapy.

ParticleX moves

We engage with you to launch clinical development and operationalize the center.

ParticleX Lead Oncologist & Clinical Director

Interested in Partnering with ParticleX ?

Tell us about your practice and we’ll get in touch.