Radiopharm Theranostics Ltd has released a press release.
RAD receives IND approval from US FDA for Betabart (RV-01)
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Radiopharm Theranostics Limited on 6ix
Story so far
Earlier from Radiopharm Theranostics
- Dr Oliver Sartor Appointed to Radiopharm Scientific Advisory Board
- Radiopharm Theranostics and Cyclotek Sign Clinical Supply Agreement for ¹⁶¹Tb-KLK3-mAb Phase I Clinical Trial in Australia
- Radiopharm Theranostics Granted U.S. Food and Drug Administration Fast Track Designation for RAD101 Imaging in Brain Metastases
- RAD Granted US FDA Fast Track for RAD101 Metastases Imaging
- Radiopharm Theranostics Doses First Patient in Phase 1 ‘HEAT’ Trial of 177Lu-RAD202 for Treatment of Advanced HER2-Positive Solid Tumors
Later from Radiopharm Theranostics
- Radiopharm Theranostics Receives IND approval from US FDA to Initiate Phase I Therapeutic Clinical Study to target B7H3 with Betabart (RV-01)
- Radiopharm Theranostics reports Fiscal Year 2025 Financial Results and Business Update
- Appendix 4E and Preliminary Final Report
- Annual Report for Fiscal Year Ending June 30, 2025 (Form 20-F)
- SPL: Research & Option Agreement with Radiopharm Theranostics
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