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Adicet Bio — Third Quarter 2026 Earnings Summary

  • **Financial Results:** Net loss narrowed to $18.9 million ($1.76/share) from $26.9 million ($4.72/share) in the prior year period, driven by a 32% reduction in R&D expenses to $15.6 million and a 17% drop in G&A to $4.2 million; cash and investments decreased to $100.9 million from $158.5 million at year-end 2025.
  • **Liquidity and Outlook:** Current cash resources are projected to fund operations through the second half of 2027, with management characterizing 2027 as a catalyst-rich year.
  • **Clinical Milestones:** Prula-cel Phase 1 data showed 50% complete renal response in lupus nephritis patients; a pivotal single-arm study is underway with enrollment expected soon, while regulatory updates and 12-month follow-up data for ~22 patients are anticipated in Q1 2027.
  • **Pipeline Progress:** The FDA granted Fast Track Designation for ADI-212 in metastatic castration-resistant prostate cancer with Phase 1 startup activities initiated and enrollment expected in Q1 2027; the first in vivo CAR-T candidate is targeted for clinic entry in H2 2027.
  • **Strategic Initiatives:** The Company plans to engage the FDA in Q4 2026 regarding potential expansion of the pivotal lupus program to include patients without nephritis.
Company
ADICET BIO INC
Sector
Healthcare
Industry
Biotechnology