Verve Therapeutics reported a net loss of $40.9 million for the second quarter of 2022. The company's cash, cash equivalents, and marketable securities totaled $293.6 million as of June 30, 2022, which, combined with proceeds from the Vertex collaboration and follow-on offering, is expected to fund operations into the second half of 2025. Patient dosing commenced for VERVE-101, and a lead development candidate, VERVE-201, was nominated.
Patient dosing is underway with VERVE-101 for Heterozygous Familial Hypercholesterolemia.
Regulatory clearances in the United Kingdom and United States are anticipated in the second half of 2022.
Preclinical data supporting nomination of ANGPTL3 development candidate, VERVE-201, will be presented at the European Society of Cardiology 2022 Congress.
A research collaboration with Vertex and an amendment to Beam License Agreement expanded the pipeline by adding two additional targets.
Verve Therapeutics expects that its cash, cash equivalents, and marketable securities as of June 30, 2022, combined with proceeds from the Vertex collaboration and follow-on offering, will be sufficient to fund its operating plan into the second half of 2025.