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Intellia retains outperform stock rating amid trial results

EditorNatashya Angelica
Published 24/10/2024, 16:24
NTLA
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On Thursday, BMO Capital maintained its Outperform rating and $70.00 price target for Intellia Therapeutics (NASDAQ:NTLA) shares. The firm's stance comes after observing the Phase II trial results of NTLA-2002, a therapy developed by Intellia for hereditary angioedema (HAE). The trial indicated an 81% reduction in attack rate compared to placebo over a period between 5 to 16 weeks, with 73% of patients remaining attack-free.

The analyst from BMO Capital noted that despite 8 out of 11 patients remaining attack-free for 42 weeks, there has been over a 15% decline in Intellia's stock. This reflects investor concerns regarding several issues.

Firstly, NTLA-2002 did not meet the expectations of having over 80% of patients attack-free. Secondly, there is a noticeable decline in the attack-free rate as the trial progressed from Phase II to Phase III, a trend seen in other HAE trials. Lastly, there is a worry that patients with severe conditions, who would benefit most from gene editing, might exhibit a lower response rate to NTLA-2002.

The analyst highlighted these concerns ahead of a key opinion leader (KOL) call scheduled for 11 am ET, which aims to provide further insights into the HAE trials and the potential of NTLA-2002. The discussion is expected to delve deeper into the data and address the investor apprehensions surrounding the efficacy and progression of the treatment.

Intellia Therapeutics is at the forefront of developing gene-editing therapies for treating genetic diseases. The outcome of the KOL call and subsequent investor sentiment will be critical for the company as it continues to advance its clinical programs and strives to meet the therapeutic needs of patients with HAE.

In other recent news, Intellia Therapeutics has seen significant developments in its clinical programs. The biotechnology company recently reported positive Phase 2 data for its investigational therapy, NTLA-2002, aimed at treating hereditary angioedema (HAE). These promising results have led to the initiation of a global pivotal Phase 3 HAELO study, which is currently recruiting patients.

In addition, Baird, a financial services firm, adjusted its outlook on Intellia shares, reducing the price target but maintaining a Neutral rating. The firm's decision followed the presentation of data from the Phase 2 study of Intellia's NTLA-2002. However, the analyst noted potential challenges for Intellia's shares, particularly in relation to the inherent risks associated with in vivo gene editing technologies.

These recent developments reflect Intellia's commitment to advancing its gene editing therapies and its robust financial position, with $939.9 million in cash reserves, expected to fund operations into late 2026.

InvestingPro Insights

Recent financial data from InvestingPro sheds additional light on Intellia Therapeutics' current position. The company's market capitalization stands at $1.66 billion, reflecting investor sentiment amidst the recent clinical trial results. Intellia's revenue for the last twelve months as of Q2 2023 was $45.97 million, with a concerning revenue decline of 13.33% over the same period.

Two key InvestingPro Tips are particularly relevant in the context of the recent trial results and market reaction. Firstly, Intellia is "quickly burning through cash," which is not uncommon for biotech companies in the development stage but could be a concern given the mixed reception of the NTLA-2002 trial results. Secondly, the tip that "11 analysts have revised their earnings downwards for the upcoming period" suggests that the market may be adjusting expectations in light of the recent data.

These insights align with the article's discussion of investor concerns and the stock's decline following the trial results. For investors seeking a more comprehensive analysis, InvestingPro offers 8 additional tips that could provide further context to Intellia'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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