Clinical Trials and Research - Acrivon reported a confirmed overall response rate (ORR) of 62.5% (95% CI, 30.4-86.5) in patients with high-grade endometrial cancer from the ongoing Phase 2b study of ACR-368[1][2][4]. - The company completed planned enrollment of the first dose-escalation cohort in the Phase 1 study of ACR-2316, which was initiated 15 months after the initial lead discovery[1][9]. - ACR-368 is positioned as a potential first approval opportunity in the second-line treatment of endometrial cancer, with ongoing evaluations for front-line setting options[5][6]. - The Phase 1 trial of ACR-2316 aims to establish safety, tolerability, and pharmacokinetic profiles, with dose optimization guided by FDA's Project Optimus[6][7]. - Acrivon anticipates providing updates from the Phase 2b trial of ACR-368 in the first half of 2025 and initial data from the Phase 1 study of ACR-2316 in the second half of 2025[7]. Financial Performance - Research and development expenses for Q3 2024 were 10.3 million in Q3 2023, primarily due to the development of ACR-368 and the initiation of the ACR-2316 clinical trial[8][9]. - The net loss for Q3 2024 was 14.5 million for the same period in 2023[8]. - Total operating expenses for Q3 2024 were 16,137,000 in Q3 2023[16]. - Research and development expenses increased to 10,267,000 in Q3 2023, reflecting a 83.6% rise[16]. - Net loss for Q3 2024 was 14,466,000 in Q3 2023, representing a 55.2% increase in losses[16]. - Comprehensive loss for Q3 2024 was 14,341,000 in Q3 2023, reflecting a 51.1% increase[16]. Cash and Assets - As of September 30, 2024, Acrivon had cash, cash equivalents, and marketable securities totaling 43,415,000 as of September 30, 2024, from 214,684,000 as of September 30, 2024, up from 196,892,000 as of September 30, 2024, compared to 2,698,000, up from 801,000, compared to a gain of $125,000 in Q3 2023[16].
Acrivon Therapeutics(ACRV) - 2024 Q3 - Quarterly Results