Crescent Biopharma (CBIO) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
30 Jul, 2026Executive 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.
Latest events from Crescent Biopharma
- Dual immuno-oncology and ADC strategy advances with CR-001 clinic entry in Q1 2026 and global ambitions.CBIO
Morgan Stanley 23rd Annual Global Healthcare Conference8 Jul 2026 - Up to $500M in securities registered, including $200M at-the-market shares via Jefferies.CBIO
Registration filing1 Jul 2026 - Four clinical studies launching this year set up a data-rich 2027 for next-gen oncology assets.CBIO
7th Annual Oncology Innovation Summit: Insights for ASCO & EHA26 Jun 2026 - CR-001 and ADC combinations target a $100B+ oncology market, with pivotal data expected in 2027.CBIO
Goldman Sachs 47th Annual Global Healthcare Conference 20268 Jun 2026 - Landmark data validate PD-1/VEGF bispecifics, driving a paradigm shift in immuno-oncology.CBIO
Jefferies Global Healthcare Conference 20264 Jun 2026 - Directors elected, auditor ratified, and executive compensation approved with annual advisory votes.CBIO
AGM 20262 Jun 2026 - Advancing next-gen IO and ADC therapies with major data readouts and strong cash runway into 2028.CBIO
Stifel 2026 Targeted Oncology Virtual Forum22 May 2026 - Global oncology programs target robust 2027 data, leveraging rapid development and broad indications.CBIO
Bank of America Global Healthcare Conference 202614 May 2026 - Net loss of $23.3M, $1M revenue, and $189.2M cash runway into 2028 as clinical programs advance.CBIO
Q1 202629 Apr 2026