Arcutis Biotherapeutics to Report Q4 2025 Earnings on February 25
Arcutis Biotherapeutics is scheduled to report fourth-quarter and full-year 2025 results on Feb. 25, after market close. Investors will focus on sales performance of Zoryve and pipeline updates.
Arcutis Biotherapeutics is scheduled to report fourth-quarter and full-year 2025 results on Feb. 25, after market close. Investors are expected to focus on the sales performance of the company's marketed drug and other pipeline updates when the company reports quarterly results.
The consensus estimate for fourth-quarter revenues is pegged at $115.7 million, while the same for earnings is pinned at 3 cents. Over the past year, shares of Arcutis Biotherapeutics have rallied 106.6% compared with the industry's growth of 18.8%.
Arcutis Biotherapeutics primarily derives product revenues from the sale of its flagship product, Zoryve (topical roflumilast), a highly potent and selective phosphodiesterase-4 (PDE4) inhibitor marketed in the United States in both cream and foam formulations. The company has been witnessing consistent growth in product sales from Zoryve, driven by sustained increases in prescription volumes across all approved indications, including plaque psoriasis, atopic dermatitis and seborrheic dermatitis, along with improved gross-to-net pricing.
The launch of Zoryve foam 0.3% for plaque psoriasis of the scalp and body boosted sales in the third quarter. In October, the FDA approved Zoryve cream 0.05% for mild to moderate atopic dermatitis in children aged two to five years. This launch is also likely to have boosted fourth-quarter sales.
The FDA accepted Arcutis's supplemental new drug application seeking approval for Zoryve cream 0.3% for treating plaque psoriasis in children aged two to five years in November. The authority has set a target action date of June 29, 2026.
Arcutis Biotherapeutics completed enrollment in an ongoing mid-stage study evaluating Zoryve cream 0.05% in infants aged three months to under 24 months with mild to moderate atopic dermatitis in November, with top-line data expected in the first quarter of 2026. Beyond its currently approved indications, Arcutis is advancing clinical programs to broaden Zoryve's label into additional indications. The company has initiated patient enrollment in mid-stage studies with Zoryve foam 0.3% for vitiligo, as well as hidradenitis suppurativa.
Fourth-quarter 2025 selling, general, and administrative expenses are expected to have increased, reflecting continued investments to support the ongoing commercial rollout of Zoryve.
Arcutis has maintained an impeccable earnings surprise track record so far. The bottom line surpassed estimates in each of the trailing four quarters, delivering an average surprise of 64.80%. In the last reported quarter, the company delivered an earnings surprise of 160%.