Apellis Q4 Loss Narrower Than Expected, Syfovre Sales Drive Revenues

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Apellis Pharmaceuticals APLS reported fourth-quarter 2024 loss of 29 cents per share, narrower than the Zacks Consensus Estimate of a loss of 39 cents. The company had incurred a loss of 73 cents in the year-ago quarter.

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Total revenues in the fourth quarter amounted to $212.5 million and surpassed the Zacks Consensus Estimate of $196 million. In the year-ago quarter, the company had reported revenues of $146.4 million.

The top line jumped 45% year over year, owing to higher sales of Syfovre (pegcetacoplan injection) in the fourth quarter. Syfovre was approved for treating geographic atrophy (GA) secondary to age-related macular degeneration by the FDA in February 2023.

More on APLS' Q4 Results

Revenues in the reported quarter included product sales of the marketed drugs — Empaveli (pegcetacoplan) and Syfovre — and licensing and other revenues under the collaboration agreement with Sobi.

Syfovre recorded sales of $167.8 million in the fourth quarter, which rose 47% year over year, owing to continued strong demand. Syfovre's sales beat the Zacks Consensus Estimate of $161.6 million as well as our model estimate of $155.5 million.

Apellis delivered more than 89,000 commercial vials and nearly 4,600 samples of Syfovre to doctors in the reported quarter. As of Dec. 31, 2024, the total number of doses of the drug delivered since its launch was 510,000. The potential approval and successful launch of Syfovre in additional geographies will add an incremental stream of revenues to APLS in the future.

In the past three months, shares of Apellis have plunged 19.7% compared with the industry’s decline of 0.6%.

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Empaveli recorded sales of $23.4 million, down 4% from the year-ago quarter’s figure, despite continued high patient compliance rates of 97%. Empaveli sales missed the Zacks Consensus Estimate of $24.2 million and our model estimate of $26 million.

Empaveli is approved in the United States for the treatment of paroxysmal nocturnal hemoglobinuria. The drug is also approved in Europe under the brand name Aspaveli for the same indication.

Licensing and other revenues came in at $21.4 million, up significantly year over year.

Research and development expenses increased 10% from the prior-year quarter’s level to $76.4 million. This was due to an increase in program-specific external costs.

Selling, general and administrative expenses totaled $121.5 million, down 14% year over year. This was due to decreases in personnel-related costs and professional and consulting fees.