PeptiDream, PDR Pharma, and Curium Complete Patient Administration in Domestic Clinical Trial for Prostate Cancer Diagnostic Candidate 64Cu-PSMA-I&T
NQ Score
82/100
N1 Content Completeness
9
Key facts
- PeptiDream, PDR Pharma, and Curium Complete Patient Administration in Domestic Clinical Trial for Prostate Cancer Diagnostic Candidate 64Cu-PSMA-I&T
- PeptiDream, PDR Pharma, and Curium announced the completion of patient administration in a domestic clinical trial aiming for the approval of the PET diagnostic candidate 64Cu-PSMA-I&T for prostate cancer. Results will support the regulatory filing along with overseas data.
- Source: PR TIMES
- Date: Fri Jun 12 2026 01:22:10 GMT+0900 (Japan Standard Time)
Direct answer
PeptiDream, PDR Pharma, and Curium announced the completion of patient administration in a domestic clinical trial aiming for the approval of the PET diagnostic candidate 64Cu-PSMA-I&T for prostate cancer. Results will support the regulatory filing along with overseas data.
- Citation
- PeptiDream, PDR Pharma, and Curium Complete Patient Administration in Domestic Clinical Trial for Prostate Cancer Diagnostic Candidate 64Cu-PSMA-I&T (Fri Jun 12 2026 01:22:10 GMT+0900 (Japan Standard Time)), PR TIMES
- Source
- PR TIMES
- Date
- Fri Jun 12 2026 01:22:10 GMT+0900 (Japan Standard Time)
AI Summary (NQ-processed)
PeptiDream, PDR Pharma, and Curium announced the completion of patient administration in a domestic clinical trial aiming for the approval of the PET diagnostic candidate 64Cu-PSMA-I&T for prostate cancer. Results will support the regulatory filing along with overseas data.
AI Analysis
Frequently Asked Questions
- Q: Who are the subjects for the 64Cu-PSMA-I&T trial?
- A: Initial Japanese prostate cancer patients with intermediate to very high risk, scheduled for surgery.
- Q: What is Curium's role in the development?
- A: Curium leads overseas development and transfers high-throughput 64Cu manufacturing technology to PDR Pharma.
- Q: What is the next step?
- A: Combining this trial's results with overseas data to file for domestic manufacturing and marketing approval.