Logotype for Crescent Biopharma Inc

Crescent Biopharma (CBIO) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Crescent Biopharma Inc

Q2 2026 earnings summary

30 Jul, 2026

Executive summary

  • Focused on developing oncology therapeutics, with lead programs CR-001 (PD-1 x VEGF bispecific antibody), CR-002 (PD-L1-directed ADC), and CR-003 (integrin beta-6-directed ADC); enrollment is progressing in multiple global Phase 1/2 trials targeting various solid tumors.

  • Initiated global Phase 1/2 trial for CR-001 and a Phase 1/2 trial for CR-003 in China; CR-002 monotherapy trial planned for H2 2026.

  • Entered major licensing and collaboration agreements with Kelun for CR-001 and SKB105 (CR-003), and with Paragon for CR-001 and CR-002; strategic collaboration with Kelun-Biotech for development and commercialization in Greater China.

  • Key clinical data readouts are anticipated beginning in Q1 2027, with several combination and monotherapy studies underway.

  • Completed reverse recapitalization and redomestication to the Cayman Islands in June 2025.

Financial highlights

  • Net loss of $24.8 million for Q2 2026 and $48.1 million for the six months ended June 30, 2026, compared to $21.8 million and $36.9 million for the same periods in 2025.

  • Revenue of $1.0 million for the six months ended June 30, 2026, from the transfer of initial supply of CR-001 to Kelun.

  • Research and development expenses increased to $19.4 million for Q2 2026, up from $12.1 million in Q2 2025, driven by pipeline development and increased headcount.

  • Cash and cash equivalents of $171.6 million as of June 30, 2026; pro forma cash was $305.1 million after the July 2026 offering.

  • Raised $143.7 million in gross proceeds ($133.5 million net) from a public offering in July 2026.

Outlook and guidance

  • Existing cash and July 2026 offering proceeds expected to fund operations into the second half of 2028.

  • Anticipates continued increase in R&D and G&A expenses as clinical programs advance and company grows.

  • Initial clinical data from CR-001 expected in Q1 2027; combination data with standard chemotherapy expected mid-2027; proof-of-concept data for CR-001, CR-002, and CR-003 anticipated in 2027.

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