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NTLA's Q4 Loss Narrower Than Estimates, Revenues Increase Y/Y

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Intellia Therapeutics NTLA incurred a fourth-quarter 2024 loss of $1.24 per share (excluding one-time expenses of change in fair value of investments), which was narrower than the Zacks Consensus Estimate of a loss of $1.32. In the year-ago quarter, Intellia had incurred a loss of $1.46 per share. Including one-time expenses, the company reported a loss of $1.27 per share in the fourth quarter of 2024.

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The company’s total revenues currently comprise only collaboration revenues. Intellia reported revenues of $12.9 million for the fourth quarter of 2024 against negative revenues of $1.9 million reported in the year-ago quarter. Revenues beat the Zacks Consensus Estimate of $9 million.

The year-over-year increase in revenues was primarily driven by collaboration revenues received under the agreement with Regeneron Pharmaceuticals REGN.

In the past year, shares of Intellia have plunged 66.9% compared with the industry’s decline of 9.2%.

 

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More on NTLA's Q4 Results

Intellia’s collaboration revenues beat our model estimate of $7.4 million.

Research and development expenses totaled $116.9 million, up 7.2% from the year-ago quarter’s figure. The increase was due to the advancement of lead pipeline programs.

General and administrative expenses increased around 11.7% year over year to $32.4 million, due to an increase in stock-based compensation.

As of Dec. 31, 2024, Intellia had cash, cash equivalents and marketable securities worth $861.7 million compared with $944.7 million as of Sept. 30, 2024. The company expects this cash balance to fund its ongoing operations into the first half of 2027.

NTLA’s Full-Year Results

For 2024, Intellia generated revenues of $57.9 million compared with $36.3 million recorded in the year-ago quarter.

For the same period, the company reported a loss of $5.25 per share, narrower than the loss of $5.42 reported in the year-ago period.

NTLA's Recent Pipeline Updates

Intellia has collaborated with Regeneron for the development of its investigational in vivo genome-editing candidate, Nexiguran ziclumeran (nex-z, also known as NTLA-2001), which is being studied for two indications, ATTR amyloidosis with polyneuropathy (ATTRv-PN) and ATTR amyloidosis with cardiomyopathy (ATTR-CM).

Nex-z is part of the company’s co-development and co-promotion agreement with Regeneron. While NTLA is the lead party in the deal for nex-z, REGN shares 25% of the development costs and commercial profits.