Jefferies 2024 Global Healthcare Conference
Logotype for Sensei Biotherapeutics Inc

Sensei Biotherapeutics (SNSE) Jefferies 2024 Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Sensei Biotherapeutics Inc

Jefferies 2024 Global Healthcare Conference summary

1 Feb, 2026

Key program highlights

  • Lead asset SNS-101 is a conditionally active, pH-sensitive antibody targeting VISTA, designed to activate only in the tumor microenvironment, reducing toxicity and improving pharmacokinetics.

  • Phase I-B study shows SNS-101 is well-tolerated, with no dose-limiting toxicities and only mild cytokine release syndrome (CRS) at high doses, overcoming issues seen with prior VISTA antibodies.

  • Early clinical signals include stable disease and tumor regression in patients with cold tumors, such as microsatellite stable colorectal and endometrial cancers, which are typically unresponsive to PD-1 therapies.

  • Dose-dependent changes in T cell populations suggest immune activation, with increased tumor-homing and cytotoxic T cells observed.

  • Cash runway extends into Q4 2025, supporting ongoing dose expansion and phase II planning.

Clinical data and safety

  • 34 patients enrolled in phase I, with 85% having cold tumors; no severe CRS or dose-limiting toxicities observed.

  • SNS-101 demonstrated dose-proportional exposure and is suitable for once every 3-week dosing, with no immunogenicity detected.

  • Combination with cemiplimab (PD-1 inhibitor) showed no adverse PK interactions and was well-tolerated.

  • Notable clinical responses include a 59% tumor shrinkage in endometrial cancer and 27% in colon cancer, both microsatellite stable.

  • Expansion cohort data expected by end of 2024, with further updates planned.

Strategic outlook and rationale

  • Dose expansion phase underway, targeting 50-70 patients across monotherapy and combination arms in multiple tumor types, including both hot and cold tumors.

  • Rationale for cold tumor focus is VISTA's expression on myeloid-derived suppressor cells, which may mediate resistance to PD-1 therapies.

  • Plans to explore broader combinations, leveraging favorable safety profile; preclinical collaborations ongoing.

  • Initial data from dose expansion expected Q4 2024, with cash runway supporting operations through Q4 2025.

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