Leerink Global Healthcare Conference 2026
Logotype for AnaptysBio Inc

AnaptysBio (ANAB) Leerink Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for AnaptysBio Inc

Leerink Global Healthcare Conference 2026 summary

11 Mar, 2026

Corporate restructuring and royalty business outlook

  • Company is splitting into two entities: a royalty-focused parent and a biopharma spin-off, with the separation expected by end of April.

  • Parent will retain royalties from Jemperli and imsidolimab, with Jemperli's royalty rate escalating from 8% at $1B sales to 25% above $2.5B.

  • Jemperli's run rate is $1.4B, with GSK guiding to peak sales north of $2.7B; royalties could reach $400M by 2029.

  • Parent company expects to be cash flow positive by mid-2027, operating virtually with minimal OpEx and staff.

  • Litigation with GSK over Jemperli's development is ongoing, with a bench trial set for July 14; outcome could revert Jemperli rights.

Biopharma spin-off and pipeline development

  • Biopharma business (First Tracks Bio, ticker FSTX) will receive all employees and relevant assets, with the spin-off not contingent on litigation outcome.

  • ANB033, a CD122 antagonist, is the anchor program targeting celiac disease and EoE, both with significant unmet need.

  • ANB033 differentiates via subcutaneous dosing and strong PD effects, showing 98% elimination of CD122+ NK cells in phase Ia.

  • Celiac phase Ib trial is underway, with data expected in Q4; trial design includes gluten challenge and mucosal healing cohorts.

  • EoE program leverages similar mechanisms, aiming to address the 175,000 biologic-eligible US patients, with potential to outperform current standard Dupixent.

Clinical and strategic outlook

  • Celiac trial is enrolling globally, on track for Q4 data; EoE data expected in 2027.

  • Safety profile for ANB033 is favorable, with no significant issues observed to date.

  • Dosing strategy for ANB033 is induction-based, with potential for less frequent dosing in later trials.

  • Biopharma business aims to advance four indications to phase IIb by 2028, with flexibility to expand into additional autoimmune diseases.

  • Capital allocation between the two entities is designed to maximize shareholder value, with potential for share repurchases and further pipeline investment.

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