H.C. Wainwright 26th Annual Global Investment Conference 2024
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Tourmaline Bio (TRML) H.C. Wainwright 26th Annual Global Investment Conference 2024 summary

Event summary combining transcript, slides, and related documents.

Logotype for Tourmaline Bio Inc

H.C. Wainwright 26th Annual Global Investment Conference 2024 summary

21 Jan, 2026

Scientific rationale and clinical focus

  • TOUR006, an anti-IL-6 antibody, targets inflammation as a key driver of cardiovascular risk, with strong evidence that CRP is a superior predictor of events compared to traditional lipid markers.

  • Recent large-scale studies highlight the predictive power of CRP, LDL, and Lp(a), with CRP emerging as the most significant for cardiovascular events in healthy populations.

  • Universal screening for these biomarkers is gaining support, potentially shifting the paradigm in cardiovascular disease management.

  • IL-6 inhibition has shown deep reductions in CRP, supporting its potential as a novel therapeutic axis.

  • TOUR006 is also being developed for thyroid eye disease (TED), leveraging IL-6’s role in autoimmune inflammation.

Clinical development and trial updates

  • The phase II TRANQUILITY trial in cardiovascular disease is enrolling, with top-line data expected in the first half of 2025; primary endpoint is change in hs-CRP.

  • The phase II spiriTED trial in TED began at the end of 2023, with data expected in 2025; primary endpoint is change in proptosis at week 20.

  • Phase III TED trial will start later in 2024, with a design similar to phase II but larger and including a cohort with prior treatments.

  • Safety data for TOUR006 is robust, with no significant concerns observed to date and a safety profile consistent with other IL-6 inhibitors.

  • The company is well-capitalized, with $334 million in cash, funding operations into 2027 and covering two pivotal TED trials.

Competitive landscape and strategic outlook

  • TOUR006 may offer advantages over teprotumumab in TED, addressing broader disease endpoints and potentially preferred due to safety and administration profile.

  • The drug could expand the treated population, especially among patients not currently receiving teprotumumab.

  • Patent portfolio provides at least 12 years of exclusivity, with potential extension to 2043 and beyond.

  • External catalysts include competitor readouts in IL-6 and other classes, with a new indication announcement expected by year-end.

  • 2024 is focused on execution, with major clinical readouts anticipated in 2025.

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