Financial Performance - Acrivon Therapeutics has incurred net losses of 26.7 million for the six months ended June 30, 2024, and 2023, respectively, with an accumulated deficit of 18.8 million, compared to a net loss of 4.9 million[107]. - Net cash used in operating activities was 20.5 million for the same period in 2023, an increase of 26.5 million, up from 6.2 million[113]. - General and administrative expenses for the six months ended June 30, 2024, were 9.6 million for the same period in 2023, reflecting a 15.0 million for the three months ended June 30, 2024, compared to 4.5 million increase[108]. - General and administrative expenses were 5.0 million in the same period in 2023, marking a 2.6 million for the three months ended June 30, 2024, compared to 1.0 million[111]. Cash and Funding - As of June 30, 2024, Acrivon had cash, cash equivalents, and investments totaling 8.50 per share, raising aggregate net proceeds of 123.2 million in net cash from financing activities for the six months ended June 30, 2024, primarily from a private placement[121]. - The company plans to finance cash needs through equity offerings, debt financings, and collaborations, which may dilute existing stockholder ownership[127]. - Future capital requirements will depend on various factors, including the costs of clinical development, regulatory review, and commercialization activities[124]. - The company may require additional capital for in-licenses or acquisitions of other drug candidates[123]. Drug Development and Clinical Trials - Acrivon is advancing its lead candidate ACR-368 in a Phase 2 trial for patients with locally advanced or metastatic, recurrent platinum-resistant ovarian cancer, with initial clinical observations indicating a favorable tolerability profile[82][84]. - The ACR-368 OncoSignature test has shown a 50% confirmed objective response rate in OncoSignature-positive patients compared to 0% in OncoSignature-negative patients, with a p-value of 0.0038[85]. - The company is leveraging its AP3 platform to develop additional drug candidates, including ACR-2316, with plans to start a Phase I clinical study in Q4 2024[87]. - Acrivon has incurred significant research and development expenses, primarily related to ACR-368 and the ACR-368 OncoSignature, with costs including external research and manufacturing[98]. - The company has received Fast Track designations for ACR-368 from the FDA for specific cancer treatments, reflecting its potential therapeutic benefits[86]. - The company anticipates significant expenses and operating losses as it advances drug candidates through clinical development and seeks regulatory approval[123]. - If regulatory approval is obtained, significant commercialization expenses related to drug manufacturing, sales, and marketing are expected[123]. Regulatory and Compliance - The company remains classified as an "emerging growth company," allowing it to delay the adoption of certain accounting standards[131]. - The market value of the company's stock held by non-affiliates is less than $700 million, qualifying it as a "smaller reporting company"[133]. - The company may continue to rely on exemptions from certain disclosure requirements available to smaller reporting companies[134]. Contractual Obligations - There were no material changes to contractual obligations during the six months ended June 30, 2024, compared to the previous annual report[128].
Acrivon Therapeutics(ACRV) - 2024 Q2 - Quarterly Report