A Seamless Phase 1/2 Open-label Study to Evaluate the Safety, Determine the Maximum Tolerated Dose of Administered Activity, and Evaluate the Efficacy of the Therapeutic Radiopharmaceutical [Ac 225]-RTX-2358 in the Treatment of Relapsed or Refractory Sarcoma
Latest Information Update: 08 Mar 2026
At a glance
- Drugs Actinium-225 RTX 2358 (Primary) ; Copper-64 LNTH 1363S (Primary)
- Indications Soft tissue sarcoma
- Focus Adverse reactions
- Acronyms ATLAS
- Sponsors Ratio Therapeutics
Most Recent Events
- 27 Feb 2026 Planned number of patients changed from 26 to 30.
- 27 Feb 2026 One more primary safety end-point is added.
- 16 Dec 2025 According to the Ratio Therapeutics Media Release, company announced today that dosing of the first cohort has been completed in the ATLAS trial.