EANM 2025 | C-Ray’s ²²⁵Ac Studies Featured as Top Oral Presentations at EANM 2025.

 

 

From October 4th to 8th, 2025, the global nuclear medicine community will gather in Barcelona, Spain, for the highly anticipated annual event—the European Association of Nuclear Medicine (EANM) Annual Congress 2025. This year's congress is particularly significant as it marks the 40th anniversary of EANM's founding.

C-Ray Therapeutics will actively participate in this milestone event by presenting multiple innovative achievements. Through cutting-edge academic presentations, interactive booth exchanges, and a relaxed Happy Hour networking event, we look forward to engaging with global experts and scholars to discuss the future of nuclear medicine.

 

C-Ray Therapeutics is evolving from an active participant into a contributor of innovative solutions and a driver of industry dialogue, increasingly integrating into the global advancement of nuclear medicine. We sincerely invite all colleagues to visit us at Booth #123 in Barcelona. Let's join hands to explore cutting-edge technologies and foster the growth of our field together.

 

 

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Academic Spotlight

Two Studies Selected as Top Rated Oral Presentations

Two studies on ²²⁵Ac-PSMA-CY313 in the field of metastatic castration-resistant prostate cancer (mCRPC), supported by C-Ray Therapeutics, have been highly recognized by the Congress Review Committee for their innovation and significant value. They have been selected as "Top Rated Oral Presentations". This achievement signifies that China's exploration in the forefront of radiopharmaceuticals is gaining increasing international attention.

 

We cordially invite you to attend the following two sessions to learn about the latest data and engage with our team of scientists:

 

 

 

 

Presentation 1: Feasibility Exploration in Dosimetry Study

Title:Feasibility study of 225Ac-PSMA-CY313 dosimetry in mCRPC patients using SPECT

SessionCutting Edge Science Track - Quantification and Innovation in Dosimetry 

Abstract No:OP-594

Venue:Room 211

Date & TimeTuesday, October 7, 9:45 - 11:15

 

 

Presentation 2: Preliminary Results on Efficacy and Safety

Title:Evaluation of the safety and efficacy of 225Ac-PSMA-CY313 in metastatic castration-resistant prostate cancer: preliminary results

SessionTheranostics Track - Prostate Cancer Therapy: Novel Probes

Abstract No:OP-671

Venue:Room 117

Date & TimeTuesday, October 7, 15:00 - 16:30

 

 

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Exhibition Booth Engagement

On-site Connection for One-Stop CRDMO Solutions

 

During the conference, we will have a dedicated engagement area at Booth #123. Here, you will have the opportunity for face-to-face discussions with C-Ray Therapeutics' technical and business teams. Gain in-depth insights into our comprehensive service capabilities, which encompass process development, quality research, preclinical evaluation, IND application support, as well as clinical supply and commercial cGMP manufacturing.

 

We will particularly highlight our core strengths in the supply assurance of α-emitters (such as Ac-225) and other scarce isotopes, as well as our dedicated R&D platforms.

 

 

 

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Happy Hour

Unwind, Connect, and Shape the Future Together

 

To foster more relaxed industry dialogue, we will host the "C-Ray Happy Hour" networking event during the congress.

 

With a selection of fine drinks and authentic Spanish tapas, we warmly welcome both existing and new partners to join us. Let’s share insights and collaborate in the autumn ambiance of Barcelona, as we collectively chart the future of nuclear medicine.

 

 

Time: October 5, 2025 (Sunday) 16:00 - 18:00
Location: C-Ray Therapeutics Booth (Booth #123)

 

For more exciting updates on our global activities, feel free to scan the QR code below to follow our LinkedIn account ⬇️

 
 
 

 

Introduction to C-Ray Therapeutics

 

C-Ray Therapeutics is dedicated to delivering end-to-end solutions for innovative radiopharmaceuticals to clients around the world. Our services span process development, quality research, preclinical evaluation, IND Enabling, clinical supply, and commercial scale cGMP production, all backed by a reliable, robust logistics network.  As of 2024, we have raised over USD 187 million in total funding.

 

C-Ray has 28,000 square-meter, state-of-the-art, world class R&D and cGMP manufacturing facilities with the highest Class A Radiation Safety License allowing commercial scale operational volume of over 30+ radioisotopes. GLP-like preclinical study center has both small and large lab animal use permit with animal feeding and administration lab, animal PET/CT for imaging, gama counter and pathology lab for biodistribution and dosimetry analysis.

 

C-Ray has successfully delivered and continues to operate 50 CRDMO projects, including 35 preclinical and molecular imaging CRO projects and 15 CDMO projects. Among these, 6 have entered the IND and IND-enabling stages, 7 have advanced to investigator-initiated trials (IITs), and 2 have entered the clinical supply stage, with 1 of them successfully progressing to a Phase III clinical study. The company has achieved comprehensive coverage of all critical links across the entire radiopharmaceutical R&D and manufacturing chain.
 

As a dedicated CRDMO partner in radiopharmaceuticals, one of our core strengths is a stable, diversified supply of radionuclides. We are actively developing high-quality domestic sources while playing a leading role in integrating and fortifying the global supply chain—most notably securing access to challenging isotopes such as Ac-225. To date, we have supported the development of 14 Ac-225–labeled projects.

 

Committed to empowering the industry, C-Ray Therapeutics is building an open, integrated “production–academia–research–application” platform. By pooling resources across the value chain and pioneering critical radiopharmaceutical technologies, we accelerate the clinical translation of integrated diagnostic & therapeutic solutions. Our goal is to drive innovation and industrial upgrading in the radiopharmaceutical sector, establishing ourselves as a global benchmark in the field.

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Created on:2025-09-30

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