Adverum shares hold strong price target, outperform rating on early study data

Published 03/10/2024, 13:10
Adverum shares hold strong price target, outperform rating on early study data

On Wednesday, Mizuho maintained its Outperform rating and $20.00 stock price target for Adverum Biotechnologies (NASDAQ:ADVM), traded on NASDAQ:ADVM. Adverum announced a promising update, stating that the top-line results from its 52-week Phase 2 LUNA study for ixo-vec, a gene therapy for wet Age-related Macular Degeneration (wAMD), will be available sooner than anticipated, now expected in the fourth quarter of 2024 instead of the first quarter of 2025.

The study's data will include all available safety information. This advancement follows positive 26-week LUNA data presented in July, which supported the potential of ixo-vec as a leading gene therapy in the wAMD market, valued at approximately $15 billion.

The accelerated timeline for ixo-vec's study results is seen as an incremental positive for Adverum. This news comes in the wake of evaluating competing wAMD gene therapy data from 4D Molecular Therapies, which did not meet the same level of efficacy as Adverum's candidate. The anticipation for ixo-vec is high, as it is believed to have best-in-class potential within its market.

Adverum is also expected to provide updates on its Phase 3 pivotal program in the fourth quarter of 2024. As the company approaches these critical updates, Mizuho's Outperform rating reflects confidence in Adverum's progress and the potential of its lead asset, ixo-vec.

Investors and industry observers are now looking forward to the fourth quarter of 2024, when more comprehensive data from the LUNA study will be revealed, potentially confirming ixo-vec's status as a frontrunner in the treatment of wAMD.

In other recent news, Adverum Biotechnologies reported robust second-quarter financial results for 2024, with earnings per share of ($0.89) surpassing both firm and consensus estimates. Truist Securities revised its price target from $60.00 to $40.00 due to concerns about safety and funding for the company's Phase 3 clinical trials.

In addition, Adverum's gene therapy candidate, Ixo-vec, has been awarded the Regenerative Medicine Advanced Therapy (RMAT) designation by the U.S. Food and Drug Administration. Analyst firms TD Cowen and H.C. Wainwright also maintained their Buy ratings on Adverum, indicating confidence in the company's promising clinical trial results and upcoming milestones.

Oppenheimer maintained its Outperform rating and $28.00 price target, reflecting confidence in Adverum's ongoing clinical developments. These recent developments highlight the firm's advancements in gene therapy treatments for ocular diseases and the significant interest from stakeholders in the company's progress.

InvestingPro Insights

As Adverum Biotechnologies (NASDAQ:ADVM) approaches its critical data readout for ixo-vec, InvestingPro data provides additional context for investors. The company's market capitalization stands at $141.86 million, reflecting the market's current valuation of its potential in the $15 billion wAMD market.

InvestingPro Tips highlight that Adverum holds more cash than debt on its balance sheet, which could be crucial for funding its ongoing clinical trials and potential commercialization efforts. Additionally, analysts anticipate sales growth in the current year, aligning with the company's progress in its clinical pipeline.

However, it is important to note that Adverum is currently trading near its 52-week low, with a significant 48.91% price decline over the past six months. This volatility underscores the high-stakes nature of biotechnology investments, especially as the company approaches key clinical milestones.

For investors seeking a deeper dive into Adverum's financials and prospects, InvestingPro offers 11 additional tips, providing a more comprehensive analysis of the company's position in the competitive gene therapy landscape.

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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