Goldman Sachs 45th Annual Global Healthcare Conference
Logotype for Bicycle Therapeutics plc

Bicycle Therapeutics (BCYC) Goldman Sachs 45th Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Bicycle Therapeutics plc

Goldman Sachs 45th Annual Global Healthcare Conference summary

1 Feb, 2026

Platform overview and differentiation

  • Utilizes a small, synthetic constrained peptide platform based on Nobel Prize-winning science, enabling delivery to targets inaccessible to larger molecules.

  • Platform allows for fine-tuning by disease and indication, supporting applications in toxin conjugates, immuno-oncology, and radionuclide therapies.

  • Demonstrates a differentiated safety profile, with clinical data in hundreds of patients showing improved tolerability and potential to address undruggable targets.

  • Lead asset BT8009 targets Nectin-4 and is in global phase II/III trials, with additional assets BT5528 (EphA2) and BT7480 (Nectin IO, CD137) in development.

  • Multiple catalysts and milestones are expected in the second half of the year across the pipeline.

Recent clinical data and ASCO highlights

  • ASCO data highlighted enhanced safety and precision of Bicycles, with PK profiles showing short systemic half-life but prolonged tumor exposure.

  • BT8009 and BT5528 demonstrated similar PK profiles, indicating platform stability across targets.

  • Clinical data for BT8009 showed a 38% response rate and 11.1 months duration of response, potentially exceeding competitor benchmarks.

  • Safety profile for BT8009 showed no grade 3 toxicities in key adverse events among 113 patients, with lower incidence of all-grade events compared to competitors.

  • Median dose intensity for BT8009 is about 90%, higher than competitors, supporting longer treatment duration.

Duravelo-2 trial design and regulatory strategy

  • Duravelo-2 is a phase II/III global trial with 300 sites, studying two doses in first-line and second-line settings, using avelumab and chemo as comparators.

  • Primary accelerated endpoint is overall response rate; secondary endpoints include PFS and OS.

  • Trial design aligned with FDA guidance and Project FrontRunner, aiming for robust evidence without shortcuts.

  • Trial began in Q1 2024, with evolving standards of care considered in design and comparator selection.

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