Bristol Myers Squibb’s $4.1bn RayzeBio acquisition delivers clinical milestone
Bristol Myers Squibb's RYZ101 meets its Phase 3 endpoint after lutetium-177 treatment, advancing alpha radiopharmaceutical development.
Bristol Myers Squibb's RYZ101 meets its Phase 3 endpoint after lutetium-177 treatment, advancing alpha radiopharmaceutical development.
GE HealthCare has moved StarGuide GX toward the U.S. market as radiopharmaceutical therapy expands beyond conventional nuclear medicine. The 4D CZT SPECT/CT system is designed to image across a wide energy range, including investigational alpha emitters, highlighting how the theranostics boom is creating demand not just for drugs but for quantitation, dosimetry and workflow infrastructure.
FDA clears Full-Life’s actinium-225 FL-261 for Phase 1 testing in c-MET-positive lung cancer as the radiopharmaceutical company expands its pipeline.
Radiotheranostics pairs molecular imaging with targeted radioactive drugs, allowing clinicians to confirm whether a tumor carries the therapeutic target before delivering radiation systemically.
Actinium advances Actimab-A IP and manufacturing while NYSE American compliance adds a parallel financing and execution test.
CONV01-α is targeting the post-Lu-PSMA prostate cancer gap. Convergent now faces the Phase 3 test that will decide its real value.
Actinium’s science story is widening, but its balance sheet pressure is now impossible to ignore. ATNM-400 data may decide the next chapter.
Find out how Niowave’s $75m Michigan facility could reshape Actinium-225 supply for targeted cancer therapies.
Radiopharma needs more than promising targets. Full-Life’s US$150m raise puts actinium-225 supply and clinical execution in focus.
Convergent Therapeutics will present Phase 2 CONV01-alpha data at ASCO 2026. Find out what this could mean for post-Lu-PSMA prostate cancer care.