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Rocket stock target raised by Canaccord, highlights completed patient enrollments

EditorAhmed Abdulazez Abdulkadir
Published 11/11/2024, 16:22
RCKT
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On Monday (NASDAQ:MNDY), Canaccord Genuity adjusted its price target for Rocket Pharmaceuticals (NASDAQ:RCKT), increasing it to $39.00 from the previous $38.00, while reiterating a Buy rating on the stock. The firm's analyst highlighted Rocket's third-quarter earnings for 2024, noting that the company's pipeline updates are largely on track. The analyst's remarks also included the completion of patient enrollment in the Phase 2 trial of RP-A501 for Danon disease earlier in September.

Rocket Pharmaceuticals also completed patient enrollment in the Phase 1 trial for RP-A601, which addresses PKP2-ACM. The company anticipates preliminary data from this trial to be available in the first half of 2025. Despite a slight delay in the approval of Kresladi, now expected in 2025 rather than the end of 2024, Canaccord Genuity expressed confidence that Rocket Pharmaceuticals will resolve the issues at hand.

The company has also begun a rolling Biologics License Application (BLA) with the U.S. Food and Drug Administration for RP-L102, a treatment for Fanconi Anemia. The regulatory review for this treatment continues with the European Medicines Agency (EMA). Canaccord Genuity has updated its model to reflect the third-quarter results of 2024 and maintains a positive outlook on Rocket Pharmaceuticals' stock.

In other recent news, Rocket Pharmaceuticals has made significant strides in its clinical trials and board appointments. The biotech firm has successfully completed the enrollment phase for its pivotal Phase 2 trial of RP-A501, a drug candidate developed to treat Danon disease, as confirmed by both Canaccord Genuity and Morgan Stanley (NYSE:MS). This major milestone sets a clear timeline for the anticipated study results, expected by the end of 2025.

In addition, Rocket Pharmaceuticals has welcomed Dr. Mikael Dolsten to its Board of Directors, a move that has been positively received by industry analysts. The company has also received a Complete Response Letter from the FDA regarding its Biologics License Application for KRESLADI™, a gene therapy designed to treat severe leukocyte adhesion deficiency-I. Despite this, Canaccord Genuity remains optimistic that the issues will be addressed satisfactorily.

Furthermore, Canaccord Genuity has maintained its Buy rating on Rocket Pharmaceuticals, with a steady price target of $38.00, while Morgan Stanley maintains an Overweight rating and a $45.00 price target. The adjustments to these price targets are influenced by the prospects of the company's Phase 3 clinical trial for its DESCARTES-08 drug candidate.

InvestingPro Insights

To complement Canaccord Genuity's optimistic outlook on Rocket Pharmaceuticals (NASDAQ:RCKT), InvestingPro data provides additional context for investors. Despite the company's promising pipeline and recent enrollment completions, it's important to note that Rocket is not currently profitable. InvestingPro Tips indicate that the company suffers from weak gross profit margins and is not expected to be profitable this year.

However, Rocket's financial position shows some strength. An InvestingPro Tip reveals that the company holds more cash than debt on its balance sheet, which could provide flexibility as it advances its clinical trials and awaits regulatory decisions. This aligns with another tip stating that Rocket's liquid assets exceed short-term obligations, potentially offering a financial cushion during the development phases of its treatments.

The market seems to be pricing in future potential, as evidenced by the price-to-book ratio of 4.82. This suggests investors are willing to pay a premium relative to the company's book value, possibly due to the promising pipeline highlighted in the article.

For investors seeking a more comprehensive analysis, InvestingPro offers 6 additional tips for Rocket Pharmaceuticals, providing a deeper understanding of the company's financial health and market position.

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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