Werewolf Therapeutics, Inc. reported a net loss of $70.5 million for the fiscal year ended December 31, 2024, compared to a net loss of $37.4 million in 2023. Revenue for 2024 totaled $1.9 million, significantly down from $19.9 million in 2023. The decrease in revenue is attributed to the completion of material performance obligations under the Collaboration Agreement with Jazz Pharmaceuticals Ireland Limited in June 2024, resulting in the recognition of all deferred revenue by year-end. Research and development expenses increased by $14.7 million to $56.4 million in 2024, primarily due to increased manufacturing and clinical trial costs for WTX-124 and WTX-330.

Significant developments during the year included updated interim data releases for the Phase 1/1b clinical trial of WTX-124, including the selection of a recommended dose for expansion, and the initiation of dose expansion arms. Initial data from combination therapy dose escalation cohorts were also reported. For WTX-330, initial Phase 1 clinical trial data were reported in June 2024, with updated interim safety and efficacy data presented at the Society for Immunotherapy of Cancer Annual Meeting in November 2024. An amended IND for WTX-330 was submitted, and a Phase 1/2 trial is expected to begin in the first quarter of 2025. The company also presented preclinical data for WTX-712 and WTX-518 at the American Association for Cancer Research annual meeting.

The company's pipeline includes WTX-124 (IL-2 INDUKINE molecule), WTX-330 (IL-12 INDUKINE molecule), WTX-712 (IL-21 INDUKINE molecule), WTX-518 (IL-18 INDUKINE molecule), and WTX-921 (IL-10 INDUKINE molecule). JZP898 (IFNα INDUKINE molecule) was licensed to Jazz Pharmaceuticals. As of December 31, 2024, Werewolf had 46 full-time employees, 33 of whom were engaged in research and development. The company's strategy focuses on advancing WTX-124 and WTX-330 through clinical development, advancing other candidates through preclinical development, and establishing a leading position in protein engineering.

Werewolf Therapeutics ended 2024 with $111.0 million in cash and cash equivalents, which the company expects will fund operations through at least the second quarter of 2026. However, the company anticipates needing substantial additional funding to complete the development and commercialization of its product candidates. Funding sources may include public or private equity offerings, debt financings, collaborations, and licensing arrangements. The company's financial performance is subject to numerous risks, including those related to clinical trial outcomes, regulatory approvals, competition, manufacturing, and intellectual property protection, all of which are detailed in the 10-K filing. The company plans to meet with regulatory authorities to discuss potential registrational pathways for WTX-124 in the second half of 2025 and release a clinical data update in the fourth quarter of 2025.

About Werewolf Therapeutics, Inc.

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