Prelude Therapeutics reported a net loss of $127.2 million for the full year 2024, with research and development expenses increasing to $118.0 million. The company anticipates its existing cash runway will fund operations into the second quarter of 2026.
PRT3789 demonstrated clinical proof-of-concept with monotherapy anti-tumor activity in SMARCA4-deficient NSCLC, gastric, and esophageal cancer.
Enrollment for PRT3789 monotherapy dose escalation is nearing completion, with additional results expected in the second half of 2025.
Enrollment for the Phase 1 study of PRT7732 is on track, with an interim data update anticipated in the second half of 2025.
The company's cash runway is projected to extend into the second quarter of 2026, with $133.6 million in cash, cash equivalents, and marketable securities as of December 31, 2024.
Prelude Therapeutics expects to continue advancing its SMARCA2 degrader development program, with data updates from ongoing clinical trials and an update on its emerging discovery pipeline.