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Relay Therapeutics Reports First Quarter 2026 Financial Results and Corporate Updates

  • FDA granted Breakthrough Therapy designation to zovegalisib for PIK3CA-mutant, HR+/HER2- advanced breast cancer in the Phase 3 ReDiscover-2 trial population
  • Phase 3 dose data for zovegalisib doublet in CDK4/6-experienced patients showed 11.1-month median PFS with similar efficacy across kinase & non-kinase mutations
  • Zovegalisib plus atirmociclib selected as go-forward triplet regimen for 1L breast cancer with Phase 3 trial in endocrine-sensitive patients expected to start in early 2027
  • Pfizer agreed to supply atirmociclib for the upcoming Phase 3 1L trial while Relay Therapeutics retains full global rights to zovegalisib
  • Phase 1/2 trial initiated for RLY-8161, an NRAS-selective inhibitor, in patients with NRAS-mutant solid tumors including melanoma
  • Initial vascular anomalies clinical data conference call planned for May 19 during the ISSVA World Congress 2026
  • Cash, cash equivalents & investments totaled $642.1 million as of March 31, 2026, sufficient to fund operations into 2029
  • First quarter 2026 revenue was $3.0 million compared to $7.7 million in the prior year period under a license agreement with Elevar Therapeutics
  • Research & development expenses were $70.6 million for the quarter, down from $73.8 million in the prior year
  • General & administrative expenses were $11.0 million for the quarter, down from $18.7 million in the prior year
  • Net loss for the first quarter of 2026 was $73.3 million, or $0.41 per share, compared to $77.1 million in the prior year