Investor presentation
Logotype for Tectonic Therapeutic Inc

Tectonic Therapeutic (TECX) Investor presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Tectonic Therapeutic Inc

Investor presentation summary

6 Aug, 2026

Strategic focus and market opportunity

  • Developing GPCR-targeted biologics for large, underserved markets in cardiovascular and rare diseases.

  • Lead asset TX45 is a long-acting relaxin targeting Group 2 PH-HFPEF, with expansion potential to PH-HFrEF and PH-ILD.

  • TX2100 is a first-in-class APJ antagonist for Hereditary Hemorrhagic Telangiectasia (HHT), a rare bleeding disorder.

  • Estimated addressable populations: ~1.4M PH-HFPEF, ~1.1M PH-HFrEF, 60K+ PH-ILD, and ~75K HHT patients in the U.S.

  • Cash runway into Q1 2029 with $227.1M as of June 2026.

Clinical pipeline and development progress

  • TX45 demonstrated positive Phase 1b results in PH-HFPEF and PH-HFrEF, showing improvements in hemodynamics and cardiac function.

  • Phase 2 APEX trial for TX45 in PH-HFPEF is ongoing, with topline results expected early Q1 2027.

  • TX45 Phase 2 trial in PH-ILD is open for screening, targeting a high-mortality, orphan population.

  • TX2100 Phase 1a trial in healthy volunteers started in Feb 2026; topline results expected by end of Q3 2026.

  • Planned Phase 1b and Phase 2 trials for TX2100 in HHT patients to assess safety and efficacy.

Scientific rationale and differentiation

  • Biologics offer advantages over small molecules for GPCR targeting, including improved selectivity and safety.

  • TX45’s mechanism addresses vasodilation, anti-fibrosis, and anti-inflammation, with monthly dosing enabled by extended half-life.

  • TX2100 targets the APJ pathway, aiming for anti-angiogenic efficacy with improved tolerability over VEGF inhibitors.

  • Preclinical models show TX2100 reduces bleeding, anemia, and vascular malformations in HHT.

  • Proprietary platform enables efficient discovery and optimization of GPCR-targeted biologics.

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