Blueprint Medicines Stock Up Despite Lower-Than-Expected Q1 Earnings

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Blueprint Medicines Corporation BPMC reported first-quarter 2025 adjusted loss of 74 cents per share, which was wider than the Zacks Consensus Estimate of a loss of 42 cents. The adjusted figure excludes the one-time equity investment gain of $50 million recorded in the reported quarter, following the closing of GSK's acquisition of IDRx. The company incurred a loss of $1.32 per share in the year-ago quarter.

Quarterly revenues of $149.4 million, generated entirely from the net product sales of Ayvakit, missed the Zacks Consensus Estimate of $171.4 million. Nonetheless, total revenues jumped 55% year over year.

Despite the earnings and revenues miss, shares of Blueprint rallied 10.9% yesterday, likely because the investors were encouraged by its guidance raise for Ayvakit’s global net product revenues in 2025. (Find the latest EPS estimates and surprises on Zacks Earnings Calendar.)

BPMC’s Q1 Results in Detail

The company’s total revenues comprise net product revenues from Ayvakit/Ayvakyt and collaboration revenues.

Ayvakit (avapritinib), an inhibitor of KIT and PDGFRA proteins, is approved for treating PDGFRA Exon 18 mutant gastrointestinal stromal tumors and advanced and indolent systemic mastocytosis (“ISM”).

Product revenues from Ayvakit sales were $149.4 million. Out of the total revenues generated from Ayvakit sales in the first quarter, $129.4 million came from the U.S. sales of the drug and $20 million in ex-U.S. sales.

Ayvakit sales have increased 61% year over year, driven by new patient starts, low discontinuation rates and a high compliance rate.

The label expansion of Ayvakit/Ayvakyt in 2023 to treat ISM in adults in the United States and European Union increased the drug's eligible patient population, which has been driving robust growth in sales. Since ISM is chronic, patients stay on therapy for longer durations.

The company did not recognize any collaboration and license revenues in the first quarter. In the year-ago quarter, the metric was $3.6 million.

Blueprint Medicines’ shares have gained 13.8% year to date against the industry’s 3.3% decline.

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Another BPMC drug, Gavreto (pralsetinib), is approved for metastatic rearranged during transfection (“RET”) fusion-positive non-small cell lung cancer and RET-mutant and RET fusion-positive thyroid cancer.

Following the severance of ties with Roche for Gavreto, Blueprint Medicines signed a deal with Rigel Pharmaceuticals in February 2024, whereby the latter purchased the U.S. rights to research, develop, manufacture and commercialize the drug. The transaction was closed in June 2024.