A Phase Ia/Ib, Open Label, Multi-center, Non-randomized Dose Escalation and Dose Expansion Study of RSC-1255 in Patients With Advanced Solid Tumor Malignancies
RSC-101 is a Phase 1a/1b clinical trial of RSC-1255 in adult study participants with advanced solid tumor malignancies who are intolerant of existing therapies known to provide clinical benefit, have disease that has progressed after standard therapy, or have previously failed other therapies. The study has two phases. The purpose of Phase 1a (Dose Escalation) is to confirm the appropriate treatment dose and Phase 1b (Dose Expansion) is to characterize the safety and efficacy of RSC-1255.
• Has pathologically confirmed advanced or metastatic malignancy characterized by one or more of the following:
‣ Participant is intolerant of existing therapy(ies) known to provide clinical benefit for their condition
⁃ Malignancy is refractory to existing therapy(ies) known to potentially provide clinical benefit
⁃ Malignancy has progressed on standard therapy
• Has evaluable or measurable tumor(s) in dose-escalation by standard radiological and/or laboratory assessments as applicable to their malignancy.
• Has adequate performance status (PS): Eastern Co-operative Oncology Group (ECOG).
• Is age ≥ 18 years.