Rocket Pharmaceuticals' Q3 Earnings Beat, Pipeline in Focus

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Rocket Pharmaceuticals, Inc. RCKT incurred a loss of 71 cents per share in the third quarter of 2024, narrower than the Zacks Consensus Estimate of a loss of 78 cents. In the year-ago quarter, the company had reported a loss of 75 cents per share.

In the absence of any marketed product in its portfolio, Rocket Pharmaceuticals did not record any revenues during the third quarter.

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More on RCKT's Q3 Results

In the reported quarter, general and administrative (G&A) expenses rose 45.7% year over year to $27.1 million. The increase was due to a rise in the company’s commercial preparation expenses, which included commercial strategy, medical affairs, legal and other expenses.

Research and development (R&D) expenses were $42.3 million, down 9.6% from the year-ago quarter’s figure. The downside was due to reduced manufacturing and development costs.

As of Sept. 30, 2024, Rocket Pharmaceuticals had cash, cash equivalents and investments of $235.7 million compared with $278.8 million on June 30, 2024. Management expects this cash balance to fund operations and meet capital expenditure requirements into 2026.

Shares of RCKT have plunged 41.8% so far this year compared with the industry’s 0.9% fall.

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RCKT's Recent Pipeline Updates

Kresladi is being developed to treat patients with severe leukocyte adhesion deficiency-I (LAD-I), a rare genetic disorder. The FDA issued a complete response letter (CRL) to the biologics license application (BLA) seeking approval for Kresladi to treat LAD-I in June 2024.

Per the CRL, the FDA sought "limited" additional information on the Chemistry Manufacturing and Controls (CMC), which is part of the BLA submission. The regulatory body is currently reviewing the limited additional CMC information for Kresladi.

RCKT expects approval for Kresladi in 2025.

Rocket Pharmaceuticals is evaluating two other gene therapies, namely RP-L102 and RP-L301, for the treatment of Fanconi anemia (“FA”) and pyruvate kinase deficiency (“PKD”), respectively.

Along with the earnings release, the company announced that it has initiated a rolling BLA for RP-L102 for treating FA. The candidate is also currently under review in the European Union for the same indication.

RP-L301 is currently being evaluated in a pivotal phase II study for treating PKD.

Rocket Pharmaceuticals is developing adeno-associated virus (AAV) gene therapies to target genetic CV indications caused by mutations or defects in different genes.