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Quince Therapeutics Reports 2024 Financial Results and Trial Progress

Quince Therapeutics Reports 2024 Financial Results and Trial Progress

Quince Therapeutics ( (QNCX) ) has released its Q4 earnings. Here is a breakdown of the information Quince Therapeutics presented to its investors.

Quince Therapeutics, Inc. is a late-stage biotechnology company focused on developing treatments for rare diseases by leveraging a patient’s own biology. The company is known for its innovative approach in the biotechnology sector, particularly in addressing unmet medical needs in rare neurological conditions.

In its latest earnings report, Quince Therapeutics provided updates on its Phase 3 NEAT clinical trial and reported financial results for the fiscal year 2024. The company highlighted that its NEAT trial has surpassed 50% enrollment, with expectations to accelerate further due to new site activations. The trial aims to evaluate the neurological effects of eDSP in patients with Ataxia-Telangiectasia (A-T), with topline results anticipated in the fourth quarter of 2025.

Key financial metrics from the report include a cash position of $40.8 million, which is expected to support operations through the Phase 3 topline results into 2026. The company reported a net loss of $56.8 million for the year, with research and development expenses amounting to $18.6 million. Strategic initiatives include a planned Phase 2 study for Duchenne muscular dystrophy and strengthening of its intellectual property portfolio.

Quince Therapeutics is also advancing its corporate strategy by expanding its scientific advisory board and engaging with investors through webinars. The company has received a Fast Track designation from the FDA for its eDSP system and continues to participate in significant scientific meetings to present its findings.

Looking ahead, Quince Therapeutics remains focused on advancing its clinical trials and exploring new funding opportunities to extend its cash runway. The management is optimistic about the potential of its lead asset, eDSP, and plans to submit regulatory applications in 2026, assuming positive clinical outcomes.

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