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.
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.
As of Dec. 31, 2024, Apellis had cash, cash equivalents and marketable securities worth $411.3 million compared with $396.9 million as of Sept. 30, 2024. APLS expects its cash balance, combined with cash anticipated from sales of marketed products, to be enough to fund its operations to profitability.
In 2024, Apellis recorded total revenues of $781.4 million, representing 97% year-over-year growth.
The company incurred a loss per share of $1.60 in 2024, narrower than the loss of $4.45 incurred in 2023.
In August 2024, Apellis and partner Sobi announced that the phase III VALIANT study evaluating systemic pegcetacoplan in C3 glomerulopathy (C3G) and primary immune complex glomerulonephritis (IC-MPGN) patients met its primary and key secondary endpoints with statistical significance.
Based on the positive data readout, Apellis recently submitted a supplemental new drug application seeking approval for pegcetacoplan in C3G and IC-MPGN. Subject to approval, the company expects the U.S. launch of Empaveli for this additional indication in the second half of 2025. A similar regulatory filing by Sobi is also currently under review by the regulatory body in the EU.
In the earnings release, Apellis stated that it is on track to initiate two phase III studies of Empaveli in focal segmental glomerulosclerosis (FSGS) and delayed graft function (DGF) in the second half of 2025. Both FSGS and DGF are rare kidney diseases in which the complement pathway plays a significant role and there are no approved therapies.
APLS also recently presented 48-month data from the GALE extension study at The Macula Society Annual Meeting in February 2025. Per the data, early monthly treatment with Syfovre in non-subfoveal patients helps preserve retinal tissue — about 1.5 disc areas in size (roughly equivalent to 2 foveal areas).
The company is also looking to initiate a mid-stage multi-dose study of siRNA candidate APL-3007 in combination with Syfovre in the second quarter of 2025, which has the potential to comprehensively block complement activity in the retina and choroid.
Apellis Pharmaceuticals, Inc. price-consensus-eps-surprise-chart | Apellis Pharmaceuticals, Inc. Quote
Apellis currently sports a Zacks Rank #3 (Hold).
Some other top-ranked stocks from the sector are Gilead Sciences GILD, BioMarin Pharmaceutical BMRN and Amicus Therapeutics FOLD, each carrying a Zacks Rank #2 (Buy) at present. You can see the complete list of today’s Zacks #1 (Strong Buy) Rank stocks here.
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BMRN’s earnings beat estimates in each of the trailing four quarters, delivering an average surprise of 32.36%.
In the past 30 days, the estimate for Amicus Therapeutics’ 2025 earnings per share has remained constant at 43 cents. The estimate for 2026 earnings per share has deteriorated from 72 cents to 71 cents. In the past three months, shares of Amicus Therapeutics have lost 3.8%.
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