Clinical TrialsThe Phase 2 trial for NGC-Cap is designed to evaluate the safety-efficacy profile of NGC-Cap versus monotherapy capecitabine, which could lead to positive advancements in treating advanced or metastatic breast cancer.
Product DevelopmentNGC-Iri, an analog of SN-38, showed a more favorable adverse event profile and greater efficacy in preclinical models compared to existing treatments, indicating potential improvements in cancer therapy.
Regulatory ApprovalProcessa Pharmaceuticals is evaluating the manufacturing process and potential sites for NGC-Iri and plans to conduct Investigational New Drug-enabling toxicology studies, indicating progress towards future approval.