Morgan Stanley 22nd Annual Global Healthcare Conference
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Cullinan Therapeutics (CGEM) Morgan Stanley 22nd Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Cullinan Therapeutics Inc

Morgan Stanley 22nd Annual Global Healthcare Conference summary

22 Jan, 2026

Strategic vision and pipeline overview

  • Focuses on transformative therapies, not incremental improvements, with five clinical programs targeting oncology and autoimmune diseases.

  • Diversified pipeline includes assets addressing disease drivers and immune system modulation.

  • Transitioned from oncology-only to include autoimmune indications, led by CLN-978.

  • Maintains $665 million in cash, providing runway into 2028 for continued pipeline advancement.

  • Modality-agnostic targeted research prioritizes target selection before modality, using a high go/no-go bar for advancing programs.

CLN-978 and autoimmune strategy

  • CLN-978, a CD19 x CD3 T cell engager, is positioned as a differentiated therapy for autoimmune diseases, starting with lupus and rheumatoid arthritis.

  • T cell engagers are seen as superior to CAR-T for broader patient access and safety, especially in younger populations.

  • CD19 is considered the optimal target due to its coverage of the B cell maturation spectrum, with high affinity for CD19 in the molecule design.

  • Early data and external studies support the efficacy and safety of T cell engagers in autoimmune settings.

  • Plans to expand CLN-978 into additional autoimmune indications, supported by strong financing.

Clinical development and differentiation

  • SLE and RA chosen as lead indications due to unmet need and strong proof-of-concept for B cell depletion therapies.

  • Initial studies focus on moderate to severe, treatment-experienced patients, aiming for disease-modifying benefits and remission.

  • Efficacy bar is set at achieving remissions and allowing discontinuation of chronic immunosuppression, with a favorable safety profile.

  • T cell engagers could be sequenced before CAR-T, with potential to move into earlier lines of therapy.

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