CRISPR stock steady with JMP’s $86 target on positive data

Published 07/05/2025, 10:00
CRISPR stock steady with JMP’s $86 target on positive data

On Wednesday, JMP analysts reaffirmed their Market Outperform rating and $86.00 price target for CRISPR Therapeutics (NASDAQ:CRSP), following the company’s announcement of promising data from its in-vivo programs. The data showcased a single dose of CTX310 leading to dose-dependent reductions in ANGPTL3 levels, as well as significant decreases in triglycerides (TG) and low-density lipoprotein (LDL) cholesterol, positioning it as a potential best-in-class option. Currently trading at $33.16, the stock has experienced significant volatility, with a beta of 1.87 and a recent one-week decline of 14.25%. InvestingPro analysis suggests the stock is currently undervalued, with 8 additional exclusive ProTips available for subscribers.

CRISPR Therapeutics has revealed that the year 2025 will be marked by several important updates across its extensive pipeline. These updates are expected to cover a range of large indications, including immuno-oncology (IO), inflammation and immunology (I&I), in-vivo editing, and diabetes treatments. JMP analysts underscored the anticipation that these developments will drive the company’s stock performance, in addition to the continued adoption of its Casgevy therapy.

The first quarter financial update of 2025 for CRISPR Therapeutics reported a robust cash position of $1.86 billion. The analysts at JMP have maintained their Market Outperform rating based on a risk-adjusted, discounted cash flow (DCF) analysis, which supports their $86 price target for the company’s stock. InvestingPro data confirms the company’s strong financial position with a current ratio of 22.07 and more cash than debt on its balance sheet. Discover detailed financial health metrics and comprehensive analysis in the exclusive Pro Research Report, available to subscribers.

The endorsement of CRISPR Therapeutics by JMP analysts comes at a time when the company is showing a strong commitment to advancing its therapeutic programs. With multiple key updates on the horizon, the company is poised for potential growth in various therapeutic areas. The financial stability indicated by the reported cash reserves adds a layer of investor confidence in the company’s ability to sustain its developmental momentum.

CRISPR Therapeutics’ focus on leveraging its CRISPR/Cas9 technology to develop gene-based medicines for serious diseases has positioned it as a leader in the field of genetic medicine. With the company’s pipeline poised to deliver updates on its diverse range of therapeutic programs, stakeholders are watching closely for the impact these developments may have on the company’s valuation and the broader biotechnology sector. While the company faces near-term profitability challenges, InvestingPro analysis reveals a market capitalization of $2.86 billion and analyst price targets ranging from $32 to $268, reflecting the market’s varied expectations for this innovative biotech player.

In other recent news, CRISPR Therapeutics has been granted orphan drug designation by the FDA for its genetically modified CAR T cell treatment targeting follicular lymphoma. This development is significant as it encourages the creation of therapies for rare diseases. In terms of financial performance, Citi analysts have adjusted their outlook on CRISPR Therapeutics, lowering the price target to $82 while maintaining a Buy rating, highlighting the progress of Casgevy with over 50 treatment centers activated globally. However, since its launch, only about five patients have been treated with Casgevy, which is used for sickle cell disease and beta-thalassemia.

Goldman Sachs reiterated a Neutral rating on CRISPR Therapeutics, noting the company’s robust cash position and its strategic direction, including its collaboration with Vertex Pharmaceuticals (NASDAQ:VRTX). The firm is monitoring the launch progress of Casgevy and expects it to become profitable by 2026. Furthermore, CRISPR Therapeutics plans to release initial Phase 1 data for its cardiovascular assets and longer-term follow-up data for its next-generation CD19 CAR T therapy by mid-2025. Additionally, the company’s Chief Operating Officer, Julianne Bruno, will step down in April after a six-year tenure.

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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