JMP maintains Acrivon stock with $17 target following update

Published 26/03/2025, 09:52
JMP maintains Acrivon stock with $17 target following update

On Wednesday, JMP Securities reiterated its Market Outperform rating and $17.00 price target for Acrivon Therapeutics Inc (NASDAQ:ACRV) shares, which currently has a market capitalization of $168 million. According to InvestingPro data, analysts maintain a strong buy consensus with price targets ranging from $17 to $30. The firm’s analyst, Silvan Tuerkcan, provided insights following the company’s recent update on ACR-368, a treatment for metastatic endometrial cancer (mEC). The analyst noted the therapy’s promising profile in mEC, despite a drop in the objective response rate (ORR) to 35%. Tuerkcan highlighted that the results, including the median duration of response (mDoR), remain competitive in the mEC treatment landscape, particularly given the characteristics of the patient population enrolled in the study.

Tuerkcan expressed approval for Acrivon’s strategic focus on mEC while deprioritizing efforts in breast cancer (BC) and prostate cancer (PROC). The anticipation of regulatory feedback and a strategy for targeting specific patient populations was also mentioned as a positive development. The JMP analyst is looking forward to the first-in-human (FiH) data for ACR-2316, expected in the second half of 2025, and mentioned being encouraged by initial activity comments made by the company today.

Acrivon Therapeutics’ approach to drug development involves a focus on precision oncology, aiming to deliver targeted treatments to patient populations identified through proprietary diagnostics. The company’s pipeline includes candidates for various cancer indications, and the recent update on ACR-368’s performance in mEC has been a critical area of interest for analysts and investors alike.

The continuation of the Market Outperform rating and the $17.00 price target reflects JMP Securities’ confidence in Acrivon’s potential, despite the adjustments in clinical trial outcomes. InvestingPro analysis shows the company maintains a strong financial position with more cash than debt and a healthy current ratio of 12.75, though it is currently burning through cash rapidly. Investors and stakeholders in the biopharmaceutical sector will be closely monitoring Acrivon Therapeutics as it progresses through regulatory milestones and further clinical developments. Based on InvestingPro’s Fair Value analysis, the stock appears slightly undervalued at current levels.For deeper insights into ACRV’s financial health and growth prospects, including 8 additional ProTips and comprehensive valuation metrics, check out the full research report available on InvestingPro.

In other recent news, Acrivon Therapeutics announced that its ACR-368 OncoSignature assay has received Breakthrough Device designation from the U.S. Food and Drug Administration. This designation is significant as it may expedite the development and review process for this device, which aims to identify endometrial cancer patients likely to respond to ACR-368 treatment. Additionally, Acrivon Therapeutics recently appointed Adam Levy, Ph.D., M.B.A., as its new Chief Financial Officer, effective April 1, 2025, following the departure of Rasmus Holm-Jorgensen. In analyst coverage, Citizens JMP reaffirmed a Market Outperform rating on Acrivon with a $17 price target, emphasizing the company’s upcoming R&D event and its clinical-stage assets. Cantor Fitzgerald also initiated coverage with an Overweight rating, highlighting the potential of Acrivon’s AP3 platform in precision medicine. Acrivon’s AP3 platform, noted for its innovative approach to biomarker selection, has been a key factor in these positive analyst evaluations. The company’s efforts in advancing its oncology treatments and proteomics data infrastructure are being closely watched by investors and industry analysts. These developments reflect the company’s ongoing progress in its clinical trials and strategic appointments.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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