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 $18.9 million, up from $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 $22.4 million, compared to a net loss of $14.5 million for the same period in 2023[8]. - Total operating expenses for Q3 2024 were $25,140,000, up 55.7% from $16,137,000 in Q3 2023[16]. - Research and development expenses increased to $18,864,000 in Q3 2024, compared to $10,267,000 in Q3 2023, reflecting a 83.6% rise[16]. - Net loss for Q3 2024 was $22,441,000, compared to a net loss of $14,466,000 in Q3 2023, representing a 55.2% increase in losses[16]. - Comprehensive loss for Q3 2024 was $21,640,000, compared to $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 $202.8 million, expected to fund operations into the second half of 2026[1][10]. - Cash and cash equivalents increased to $43,415,000 as of September 30, 2024, from $36,015,000 at the end of 2023, showing a 9.9% growth[17]. - Total assets rose to $214,684,000 as of September 30, 2024, up from $138,265,000 at the end of 2023, indicating a 55.2% increase[17]. - Stockholders' equity increased significantly to $196,892,000 as of September 30, 2024, compared to $121,195,000 at the end of 2023, a growth of 62.3%[17]. Market Context - Approximately 30,000 new cases of high-grade endometrial cancer are diagnosed annually in the U.S., with about 90% of these patients progressing to second-line treatment[3][5]. - Interest income for Q3 2024 was $2,698,000, up from $1,768,000 in Q3 2023, marking a 52.5% increase[16]. - Weighted-average common stock outstanding increased to 38,105,131 shares in Q3 2024 from 22,081,162 shares in Q3 2023, a rise of 72.7%[16]. - Other comprehensive income for Q3 2024 included an unrealized gain of $801,000, compared to a gain of $125,000 in Q3 2023[16].

Group 1 - Acrivon Therapeutics, Inc. (ACRV) has outperformed its Medical sector peers with a year-to-date performance increase of 42.7%, compared to the average gain of 8.6% for Medical stocks [2][3] - Acrivon Therapeutics currently holds a Zacks Rank of 2 (Buy), indicating a favorable outlook based on earnings estimate revisions and improving earnings outlooks [2][3] - The Zacks Consensus Estimate for ACRV's full-year earnings has increased by 4.9% over the past quarter, reflecting improved analyst sentiment [2] Group 2 - Acrivon Therapeutics is part of the Medical - Drugs industry, which consists of 178 individual stocks and currently ranks 93 in the Zacks Industry Rank [3] - The average performance of stocks in the Medical - Drugs industry has been a loss of 3.5% this year, highlighting ACRV's relative strength [3] - Akebia Therapeutics (AKBA) is another stock in the Medical sector that has shown strong performance, with a year-to-date return of 8.9% and a Zacks Rank of 2 (Buy) [2][3]

Financial Performance - The net loss for Q2 2024 was $18.8 million, compared to a net loss of $13.9 million in Q2 2023, representing a 35% increase in losses year-over-year[6]. - The total operating expenses for Q2 2024 were $21.4 million, compared to $15.5 million in Q2 2023[13]. - The weighted-average common stock outstanding for Q2 2024 was approximately 36.1 million shares, compared to 21.9 million shares in Q2 2023[13]. Research and Development - Research and development expenses increased to $15.0 million in Q2 2024 from $10.5 million in Q2 2023, primarily due to ongoing development of ACR-368 and increased personnel costs[6]. - ACR-368 demonstrated a confirmed overall response rate (ORR) of 50% in OncoSignature-positive patients with gynecological cancers, including a 60% ORR in endometrial cancer[3]. - ACR-2316, a selective WEE1/PKMYT1 inhibitor, is on track for a Phase 1 clinical study initiation in Q4 2024[4]. - The Phase 1 clinical study of ACR-2316 will be enriched for tumor types predicted to be sensitive to monotherapy through AP3-based indication finding[5]. - The company plans to present updated clinical data for ACR-368 at the ESMO conference on September 14, 2024[5]. Funding and Financial Position - The company executed an oversubscribed private placement financing of $130 million, indicating strong investor support[4]. - As of June 30, 2024, the company had cash, cash equivalents, and marketable securities totaling $220.4 million, expected to fund operations into the second half of 2026[7].

Financial Performance - Acrivon Therapeutics has incurred net losses of $35.3 million and $26.7 million for the six months ended June 30, 2024, and 2023, respectively, with an accumulated deficit of $151.7 million as of June 30, 2024[90]. - The company expects to continue incurring significant operating losses and will require substantial additional funding to support ongoing operations and growth strategies[92]. - The net loss for the three months ended June 30, 2024, was $18.8 million, compared to a net loss of $13.9 million for the same period in 2023, reflecting an increase of $4.9 million[107]. - Net cash used in operating activities was $31.0 million for the six months ended June 30, 2024, compared to $20.5 million for the same period in 2023, an increase of $10.5 million[119]. - Research and development expenses for the six months ended June 30, 2024, totaled $26.5 million, up from $20.3 million in the same period in 2023, an increase of $6.2 million[113]. - General and administrative expenses for the six months ended June 30, 2024, were $12.6 million, compared to $9.6 million for the same period in 2023, reflecting a $3.0 million increase[114]. - Research and development expenses increased to $15.0 million for the three months ended June 30, 2024, compared to $10.5 million for the same period in 2023, representing a $4.5 million increase[108]. - General and administrative expenses were $6.4 million for the three months ended June 30, 2024, up from $5.0 million in the same period in 2023, marking a $1.4 million increase[110]. - Total other income, net was $2.6 million for the three months ended June 30, 2024, compared to $1.6 million for the same period in 2023, an increase of $1.0 million[111]. Cash and Funding - As of June 30, 2024, Acrivon had cash, cash equivalents, and investments totaling $220.4 million, expected to fund operations into the second half of 2026[93]. - Acrivon entered into a PIPE agreement to issue 8,235,000 shares at $8.50 per share, raising aggregate net proceeds of $123.8 million after fees[89]. - The company raised $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].

Company Performance - Acrivon Therapeutics, Inc. (ACRV) has gained approximately 32.5% year-to-date, outperforming the average gain of 5.3% in the Medical sector [2] - Acrivon Therapeutics, Inc. holds a Zacks Rank of 2 (Buy), indicating a favorable outlook based on earnings estimate revisions [1] - The Zacks Consensus Estimate for ACRV's full-year earnings has increased by 17% over the past three months, reflecting improved analyst sentiment [2] Industry Comparison - Acrivon Therapeutics, Inc. is part of the Medical - Drugs industry, which has seen a decline of about 9.7% year-to-date, indicating that ACRV is performing better than its industry peers [3] - In contrast, the Medical Info Systems industry, which includes Hims & Hers Health, Inc. (HIMS), has experienced a decline of 17.9% since the beginning of the year [3] - Hims & Hers Health, Inc. has achieved a remarkable return of 151.6% year-to-date and has a Zacks Rank of 1 (Strong Buy) [2]

Group 1 - Acrivon Therapeutics, Inc. (ACRV) is currently outperforming its Medical sector peers with a year-to-date gain of approximately 48.6%, compared to the average gain of 5.3% for Medical stocks [2][3] - The Zacks Consensus Estimate for ACRV's full-year earnings has increased by 17% over the past quarter, indicating improved analyst sentiment and a stronger earnings outlook [2] - Acrivon Therapeutics, Inc. holds a Zacks Rank of 2 (Buy), suggesting it has favorable characteristics for potential outperformance in the market [1] Group 2 - Acrivon Therapeutics, Inc. is part of the Medical - Drugs industry, which consists of 185 stocks and currently ranks 83 in the Zacks Industry Rank; this industry has seen an average loss of 7.2% year-to-date [3] - In contrast, Hims & Hers Health, Inc. (HIMS), another stock in the Medical sector, has achieved a year-to-date return of 134% and has a Zacks Rank of 1 (Strong Buy) [2][3] - The Medical Info Systems industry, which includes Hims & Hers Health, has 43 stocks and is ranked 72, with an average decline of 19.7% since the beginning of the year [3]

Company Overview - Acrivon Therapeutics is a precision oncology company that has made significant advancements in its proprietary Acrivon Predictive Precision Proteomics (AP3) platform in 2024 [1] - The company achieved statistically significant prospective validation of its AP3 patient selection approach through the ACR-368 OncoSignature assay, which can identify ovarian and endometrial patients sensitive to ACR-368 monotherapy [1] Pipeline Developments - Acrivon's lead pipeline candidate, ACR-368/prexasertib, a CHK1/2 inhibitor, is currently in phase II studies across multiple tumor types [1] - Initial positive clinical data from a phase II study of ACR-368 for patients with locally advanced or metastatic, recurrent platinum-resistant ovarian cancer or endometrial adenocarcinoma showed a combined overall confirmed response rate of 50%, surpassing the clinical bar necessary to improve over standard care [1] Stock Performance - Acrivon Therapeutics' stock has increased by 61.6% year to date, contrasting with a 9.3% decline in the industry [2] - The company currently holds a Zacks Rank 2 (Buy), with the consensus estimate for 2024 loss narrowing from $2.98 per share to $2.47 per share over the past 60 days [3] Other Candidates - Another candidate, ACR-2316, a WEE1/PKMYT1 inhibitor, is designed for superior single-agent activity, with clinical studies expected to commence in Q4 2024 [3] Earnings Estimates - Acrivon has beaten earnings estimates in three of the last four quarters, with an average earnings surprise of 3.56% [3]

Core Viewpoint - The Zacks Medical-Drugs industry has shown signs of recovery in early 2024 after a downturn in 2023, driven by M&A activity and innovation in key therapeutic areas, despite facing macroeconomic pressures and pipeline setbacks [1] Industry Overview - The Zacks Medical-Drugs industry consists of small to medium-sized drug companies producing medicines for human and veterinary use, often relying on collaboration payments for revenue [2] Factors Influencing the Industry - Pipeline success is crucial, as the outcomes of clinical studies can significantly impact stock prices, with successful innovations acting as catalysts [3] - Strong collaboration with larger drugmakers is essential for small pharma companies, indicating growth potential [3] - Investment in technology and personalized medicine is necessary for adapting to the evolving healthcare landscape [4] Challenges Facing the Industry - Smaller companies face risks from unstable cash flows and potential failures in key pipeline candidates, which can adversely affect share prices [5] Industry Performance Metrics - The Zacks Medical-Drugs industry currently holds a Zacks Industry Rank of 90, placing it in the top 36% of 250 Zacks industries, indicating positive prospects [6] - Over the past year, the industry has underperformed, with a collective decline of 5.4% compared to the S&P 500's increase of 27.9% [7] Valuation Insights - The industry is trading at a trailing 12-month price-to-sales ratio of 2.05, lower than the S&P 500's 4.07 and the Zacks Medical sector's 3.50 [8] Notable Companies and Their Performance - **Bioventus**: Experiencing double-digit revenue growth, with stock up 20.1% year-to-date and a consensus estimate for 2024 earnings rising from 16 cents to 27 cents per share [9][10] - **Aquestive Therapeutics**: Key pipeline candidate Anaphylm shows promise, with stock up 51.5% year-to-date and a consensus estimate for 2024 loss increasing from 38 cents to 42 cents per share [11][12] - **Cardiol Therapeutics**: Developing CardiolRx for heart disease, with stock up 163.3% year-to-date and a narrowed consensus estimate for 2024 loss from 32 cents to 26 cents per share [14][15] - **Heron Therapeutics**: Key drug Zynrelef has expanded its label, with stock up 103.5% year-to-date and a narrowed consensus estimate for 2024 loss from 22 cents to 10 cents per share [16][17] - **Acrivon Therapeutics**: Progressing in precision oncology with stock up 65% year-to-date and a narrowed consensus estimate for 2024 loss from $2.98 to $2.47 per share [19][20]

Investors interested in Medical stocks should always be looking to find the best-performing companies in the group. Acrivon Therapeutics, Inc. (ACRV) is a stock that can certainly grab the attention of many investors, but do its recent returns compare favorably to the sector as a whole? A quick glance at the company's year-to-date performance in comparison to the rest of the Medical sector should help us answer this question.Acrivon Therapeutics, Inc. is a member of our Medical group, which includes 1047 di ...

[Business Highlights](index=1&type=section&id=Business%20Highlights) Acrivon reported significant progress in Q1 2024, highlighted by the prospective validation of its AP3 patient selection platform for the ACR-368 trial, which showed a **50%** confirmed overall response rate (ORR) in OncoSignature-positive patients with ovarian and endometrial cancer, and strengthened its financial position with a **$130 million** oversubscribed private placement - Achieved statistically significant prospective validation of the AP3 patient selection platform with the ACR-368 OncoSignature assay, which effectively identifies cancer patients likely to respond to ACR-368 monotherapy[1](index=1&type=chunk) - In the ongoing Phase 2b trial of ACR-368 for platinum-resistant ovarian or endometrial cancer, a confirmed Overall Response Rate (ORR) of **50%** was observed in the prospectively-defined, OncoSignature-positive patient cohort, clearly segregating responders from the OncoSignature-negative arm (0% ORR), with a p-value of 0.0038[2](index=2&type=chunk)[3](index=3&type=chunk) - Successfully executed an oversubscribed **$130 million** private placement financing at a premium, with support from new and existing healthcare investors[1](index=1&type=chunk)[3](index=3&type=chunk) [Pipeline and Future Outlook](index=2&type=section&id=Pipeline%20and%20Future%20Outlook) The company has accelerated the development of ACR-2316, a dual WEE1/PKMYT1 inhibitor, with an IND submission planned for Q3 2024 and a Phase 1 study initiation in Q4 2024, with further pipeline updates expected in the second half of 2024 and plans to advance a new cell cycle program in 2025 - The timeline for ACR-2316, a potential first-in-class WEE1/PKMYT1 inhibitor, has been accelerated based on compelling preclinical data showing superior activity[1](index=1&type=chunk)[3](index=3&type=chunk) - Key upcoming milestones for 2024 include: - IND submission for ACR-2316 in Q3 2024 - Initiation of a Phase 1 clinical study of ACR-2316 in Q4 2024 - General pipeline and corporate updates in the second half of 2024[4](index=4&type=chunk) - The company plans to advance a new, potential first-in-class cell cycle program for an undisclosed target towards development candidate nomination in 2025[4](index=4&type=chunk) [First Quarter 2024 Financial Results](index=2&type=section&id=First%20Quarter%202024%20Financial%20Results) For the first quarter of 2024, Acrivon reported a net loss of **$16.5 million**, an increase from **$12.8 million** in the prior year's quarter, driven by higher R&D and G&A expenses, and as of March 31, 2024, the company held **$110 million** in cash and equivalents, which, combined with a subsequent **$130 million** financing, is expected to fund operations into the second half of 2026 Q1 2024 Statement of Operations Highlights (vs. Q1 2023) | Financial Metric | Q1 2024 (in thousands) | Q1 2023 (in thousands) | Change | | :--- | :--- | :--- | :--- | | Research and Development | $11,473 | $9,758 | +17.6% | | General and Administrative | $6,195 | $4,635 | +33.7% | | **Net Loss** | **$(16,486)** | **$(12,756)** | **+29.2%** | | Net Loss Per Share | $(0.73) | $(0.58) | +25.9% | - The increase in R&D expenses was primarily due to the continued development of ACR-368 and increased personnel costs, while the rise in G&A expenses was mainly due to higher personnel costs, including non-cash stock compensation[5](index=5&type=chunk) Balance Sheet and Cash Position | Metric | As of March 31, 2024 | Note | | :--- | :--- | :--- | | Cash, Cash Equivalents & Marketable Securities (in millions) | $110 | Prior to April 2024 financing | | April 2024 Private Placement (gross proceeds, in millions) | $130 | Not included in March 31 balance | | **Cash Runway** | **Into 2H 2026** | Includes proceeds from financing | [Company Overview](index=2&type=section&id=About%20Acrivon%20Therapeutics) Acrivon is a clinical-stage biopharmaceutical company focused on precision oncology, utilizing its proprietary proteomics platform, AP3, to match patients with targeted therapies, with its lead candidate, ACR-368, in a Phase 2 trial for ovarian and endometrial cancer and having received FDA Fast Track designation, while its preclinical pipeline includes ACR-2316 and another undisclosed cell cycle program - Acrivon's core technology is its proprietary Acrivon Predictive Precision Proteomics (AP3) platform, used to identify patients most likely to benefit from its drug candidates by creating drug-specific OncoSignature companion diagnostics[7](index=7&type=chunk) - The lead candidate, ACR-368 (prexasertib), is a selective CHK1/CHK2 inhibitor in a potentially registrational Phase 2 trial, having received FDA Fast Track designation for use in patients with platinum-resistant ovarian or endometrial cancer identified via its OncoSignature test[7](index=7&type=chunk) - The preclinical pipeline includes ACR-2316, a potent and selective WEE1/PKMYT1 inhibitor, and an undisclosed cell cycle program, both developed using the AP3 platform[7](index=7&type=chunk)