TScan Therapeutics reported second quarter 2024 financial results, including revenue of $0.5 million and a net loss of $31.7 million. The company received RMAT designation for TSC-100 and TSC-101 and engaged a CDMO for manufacturing. They expect to report initial data from the solid tumor program and one-year data from the ALLOHATM Phase 1 heme trial by the end of 2024 and cash is expected to fund operations into Q4 2026.
FDA granted RMAT designation to TSC-100 and TSC-101 for AML, ALL, and MDS treatment.
Engaged CDMO with global capabilities to support manufacturing for pivotal trials and commercialization.
On-track to report initial data from the solid tumor program and one-year data on initial patients in the ALLOHATM Phase 1 heme trial by the end of 2024.
Cash, cash equivalents, and marketable securities continue to fund operations into the fourth quarter of 2026.
TScan anticipates several milestones in their Heme Malignancies and Solid Tumor programs.