等待开盘 03-27 09:30:00 美东时间
-0.080
-1.85%
Radiopharm Theranostics says Phase 2b interim data showing 90% MRI concordance for RAD 101, with final readout expected by June.
03-24 22:56
Radiopharm Theranostics (ASX: RAD, "Radiopharm" or the "Company"), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need, today
03-24 19:14
Radiopharm Theranostics (ASX:RAD, "Radiopharm" or the "Company"), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need, today
02-24 20:36
Benzinga examined the prospects for many investors' favorite stocks over the last week — here's a look at some of our top stories.
2025-12-20 21:31
U.S. stocks traded mostly lower this morning, with the Dow Jones index falling ...
2025-12-16 22:56
Radiopharm Theranostics shares rise after interim Phase 2b data showed 92% MRI concordance for RAD 101 imaging in brain metastases.
2025-12-16 00:59
RADX: 471% | Radiopharm Theranostics' Interim Data From The First Twelve Patients In Its U.S. Phase 2b Imaging Trial Of RAD 101 In Brain Metastases Showed That 92% Of The Patients Achieved Concordance With
2025-12-15 20:26
Radiopharm Theranostics' RAD101 has received FDA Fast Track Designation to differentiate between recurrent brain metastases and treatment effects in a Phase 2 clinical trial.
2025-06-11 12:00
Radiopharm Theranostics has dosed the first patient in a Phase 1 trial of 177Lu-RAD202, targeting HER2-positive advanced solid tumors. The 'HEAT' trial aims to assess safety, tolerability, and efficacy of this novel radiotherapeutic, with earlier data supporting its potential. The study is conducted across Australia, targeting patients with aggressive cancers like breast, ovarian, and gastric. This milestone underscores the company's commitment to addressing unmet needs in oncology.
2025-06-04 12:00
Radiopharm Theranostics announced favorable preclinical data for RV01, a B7-H3-targeted radiopharmaceutical, showing high tumor uptake and favorable biodistribution. The modified monoclonal antibody has a shorter half-life, reducing off-target exposure and potential toxicities. IND submission is expected mid-2025, with a first-in-human Phase 1 study planned for Q4 2025.
2025-06-02 12:00