BioCryst Reports Third Quarter 2024 Financial Results and Provides Business Update
BioCryst Pharmaceuticals reported strong Q3 2024 financial results, with ORLADEYO net revenue reaching $116.3 million, a 35.7% year-over-year increase. The company achieved a GAAP operating profit of $7.7 million and adjusted its full-year 2024 ORLADEYO revenue guidance to $430-435 million. Total product revenue guidance for 2024 is set at $443-448 million. The company reported progress with BCX17725 for Netherton syndrome entering clinical trials and expects to be approaching quarterly positive EPS by second half of 2025.
BioCryst Pharmaceuticals ha riportato risultati finanziari solidi per il terzo trimestre del 2024, con un fatturato netto di ORLADEYO che ha raggiunto i 116,3 milioni di dollari, un incremento del 35,7% rispetto all'anno precedente. L'azienda ha ottenuto un utile operativo GAAP di 7,7 milioni di dollari e ha aggiornato le previsioni di fatturato per ORLADEYO per l'intero anno 2024 a 430-435 milioni di dollari. La guida per il fatturato totale dei prodotti per il 2024 è fissata tra 443 e 448 milioni di dollari. L'azienda ha segnalato progressi con BCX17725 per la sindrome di Netherton, che sta entrando in sperimentazione clinica e prevede di raggiungere un utile per azione trimestrale positivo nella seconda metà del 2025.
BioCryst Pharmaceuticals informó sobre resultados financieros sólidos para el tercer trimestre de 2024, con ingresos netos de ORLADEYO alcanzando los 116.3 millones de dólares, un incremento del 35.7% en comparación con el año anterior. La compañía logró un beneficio operativo GAAP de 7.7 millones de dólares y ajustó su guía de ingresos para ORLADEYO para todo el año 2024 a 430-435 millones de dólares. La previsión de ingresos totales por productos para 2024 se establece entre 443 y 448 millones de dólares. La empresa reportó avances con BCX17725 para el síndrome de Netherton, ingresando a ensayos clínicos y espera acercarse a un EPS positivo trimestral en la segunda mitad de 2025.
BioCryst Pharmaceuticals는 2024년 3분기 강력한 재무 결과를 보고했습니다. ORLADEYO의 순수익은 1억 1630만 달러에 달하며, 이는 전년 대비 35.7% 증가한 수치입니다. 회사는 GAAP 운영 이익 770만 달러를 달성했으며, 2024년 전체 ORLADEYO 수익 가이드를 4억 3000만~4억 3500만 달러로 조정했습니다. 2024년 총 제품 수익 가이드는 4억 4300만~4억 4800만 달러로 설정되었습니다. 이 회사는 Netherton 증후군에 대한 BCX17725의 진행 상황을 보고하며, 임상 시험에 진입했으며 2025년 하반기에는 분기별로 긍정적인 EPS에 도달할 것으로 예상하고 있습니다.
BioCryst Pharmaceuticals a annoncé des résultats financiers solides pour le troisième trimestre 2024, avec des revenus nets de ORLADEYO atteignant 116,3 millions de dollars, soit une augmentation de 35,7 % par rapport à l'année précédente. L'entreprise a réalisé un bénéfice opérationnel GAAP de 7,7 millions de dollars et a ajusté ses prévisions de revenus pour ORLADEYO pour l'ensemble de l'année 2024 à 430-435 millions de dollars. Les prévisions de revenus totaux pour les produits pour 2024 sont fixées entre 443 et 448 millions de dollars. L'entreprise a signalé des progrès avec BCX17725 pour le syndrome de Netherton, qui entre dans les essais cliniques, et s'attend à atteindre un bénéfice par action positif trimestriel au cours de la seconde moitié de 2025.
BioCryst Pharmaceuticals berichtete über starke Finanzzahlen im dritten Quartal 2024, mit einem Nettoumsatz von ORLADEYO, der 116,3 Millionen Dollar erreicht, was einem Anstieg von 35,7% im Vergleich zum Vorjahr entspricht. Das Unternehmen erzielte einen GAAP-Betriebsgewinn von 7,7 Millionen Dollar und passte seine Umsatzprognose für ORLADEYO für das Gesamtjahr 2024 auf 430-435 Millionen Dollar an. Die Gesamteinnahmenprognose für Produkte für 2024 beträgt zwischen 443 und 448 Millionen Dollar. Das Unternehmen berichtete von Fortschritten bei BCX17725 für das Netherton-Syndrom, das in die klinische Erprobung eingetreten ist, und erwartet, in der zweiten Hälfte von 2025 einen positiven EPS pro Quartal zu erreichen.
- ORLADEYO Q3 revenue grew 35.7% y-o-y to $116.3 million
- Achieved GAAP operating profit of $7.7 million ($24.9 million non-GAAP)
- Increased reimbursed product rate in U.S. to 74.8%
- Operating cash increased by $13.1 million in Q3
- Raised full-year ORLADEYO revenue guidance to $430-435 million
- Net loss of $14.0 million in Q3 2024
- Interest expense of $24.8 million in Q3
- SG&A expenses increased 28.7% y-o-y to $65.1 million
- Cash position decreased to $351.7M from $399.2M year-over-year
Insights
The Q3 results demonstrate remarkable commercial success with
Key financial improvements include reduced R&D expenses (
The pipeline developments show strategic diversification beyond ORLADEYO. BCX17725 entering clinical trials for Netherton syndrome addresses an unmet need in a rare genetic disorder with no approved treatments. The avoralstat program for DME represents a novel approach targeting the kallikrein-bradykinin pathway, potentially offering advantages over current VEGF inhibitors in terms of treatment frequency and efficacy.
ORLADEYO's commercial success is supported by real-world efficacy data, with approximately half of patients switching from other prophylactic therapies. The initiation of the APeX-T observational study will provide valuable insights into optimal transition strategies, potentially further strengthening market position and supporting the
— Q3 2024 ORLADEYO net revenue of
— Full-year 2024 ORLADEYO revenue guidance adjusted to
— Company introduces full-year 2024 total product revenue guidance of
— BCX17725 for Netherton syndrome advances into the clinic —
— Company generates GAAP operating profit of
RESEARCH TRIANGLE PARK, N.C., Nov. 04, 2024 (GLOBE NEWSWIRE) -- BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today reported financial results for the third quarter ended September 30, 2024, and provided a corporate update.
“Our third quarter performance continues to build on the outstanding year we are having, with significant revenue growth, strong patient demand, pipeline advancement and operating profitability in the quarter. As we look ahead, we see robust and durable revenue growth, new opportunities for younger children to benefit from ORLADEYO, and data readouts from BCX17725 in Netherton syndrome and avoralstat in DME, all while moving closer to sustainable profitability,” said Jon Stonehouse, president and chief executive officer of BioCryst.
Program Updates
ORLADEYO® (berotralstat): Oral, Once-daily Treatment for Prevention of Hereditary Angioedema (HAE) Attacks
“The real-world efficacy and convenience patients and physicians are experiencing with ORLADEYO are driving accelerated commercial momentum that translates to nearly 36 percent revenue growth in our fourth year on the market. Based on this established sales trajectory, and the continued, durable strength of patient demand we see for ORLADEYO, we are more confident than ever of achieving peak sales of
- ORLADEYO net revenue in the third quarter of 2024 was
$116.3 million (+35.7 percent year-over-year (y-o-y)). - Start forms in the U.S. are up 14.2 percent over the past 12 months compared to the prior 12 months; and 67 new U.S. prescribers were added during the third quarter, one of the highest totals over the most recent eight quarters.
- The reimbursed product rate in the U.S. increased 0.4 percent in the third quarter to 74.8 percent.
- Sales from outside the U.S. contributed 11.4 percent of global ORLADEYO net revenues in the third quarter.
- Since launch, approximately half of patients who have started ORLADEYO have switched from another prophylactic therapy. The company has begun the observational Phase 4 APeX-T study, designed to generate real-world data to inform physicians on the best individual approaches to support transition to ORLADEYO.
Rare Disease Pipeline
“The goal with our pipeline is to build on our success with ORLADEYO by bringing the next highly differentiated product to patients living with rare disease. We are making excellent progress, with BCX17725 now in the clinic, avoralstat nearing the clinic and initial patient data from both programs expected next year. These programs would address significant unmet needs for patients with Netherton syndrome and DME, respectively,” said Dr. Helen Thackray, chief research and development officer at BioCryst.
- The company has advanced BCX17725, its KLK5 inhibitor for the treatment of Netherton syndrome, into clinical trials and expects initial data from the program in 2025.
- Netherton syndrome is a serious, rare, lifelong genetic disorder affecting the skin, hair, and immune system, caused by lack of normal function of a natural inhibitor of KLK5. People with Netherton syndrome often have red, scaly, inflamed skin, fragile hair, and are more likely to develop skin infections, allergies, asthma and eczema. Netherton syndrome can be life threatening, especially during infancy when patients are vulnerable to dehydration and recurrent infections. Currently, there are no approved treatments for Netherton syndrome.
- Netherton syndrome is a serious, rare, lifelong genetic disorder affecting the skin, hair, and immune system, caused by lack of normal function of a natural inhibitor of KLK5. People with Netherton syndrome often have red, scaly, inflamed skin, fragile hair, and are more likely to develop skin infections, allergies, asthma and eczema. Netherton syndrome can be life threatening, especially during infancy when patients are vulnerable to dehydration and recurrent infections. Currently, there are no approved treatments for Netherton syndrome.
- In 2025, the company plans to advance avoralstat, a plasma kallikrein inhibitor, into a clinical trial of patients with diabetic macular edema (DME).
- DME is an important cause of vision loss in diabetes and is due to leakage from the blood vessels in the retina. While current treatments focus on VEGF inhibition, DME can develop from other mechanisms, such as the kallikrein-bradykinin pathway. This is supported by observations that many DME patients have an incomplete response to intravitreal anti-VEGF therapies that are administered every four to eight weeks. Avoralstat targets the kallikrein-bradykinin system on the retinal vascular endothelial cells and may result in less vascular leakage and less edema. Avoralstat, delivered to the suprachoroidal space as a depot formulation, is designed to provide high dose levels to the retinal vessels with long-lasting exposure, which could result in less frequent injections and a reduced burden on patients and the healthcare system.
- DME is an important cause of vision loss in diabetes and is due to leakage from the blood vessels in the retina. While current treatments focus on VEGF inhibition, DME can develop from other mechanisms, such as the kallikrein-bradykinin pathway. This is supported by observations that many DME patients have an incomplete response to intravitreal anti-VEGF therapies that are administered every four to eight weeks. Avoralstat targets the kallikrein-bradykinin system on the retinal vascular endothelial cells and may result in less vascular leakage and less edema. Avoralstat, delivered to the suprachoroidal space as a depot formulation, is designed to provide high dose levels to the retinal vessels with long-lasting exposure, which could result in less frequent injections and a reduced burden on patients and the healthcare system.
Third Quarter 2024 Financial Results
“It is exciting to see continued ORLADEYO growth alongside the significant progress advancing our pipeline, and another quarter of operating profit. BioCryst is in the strongest financial position in its history,” said Anthony Doyle, chief financial officer at BioCryst.
For the three months ended September 30, 2024, total revenues were
Research and development expenses for the third quarter of 2024 decreased to
Selling, general and administrative expenses for the third quarter of 2024 increased to
Interest expense was
GAAP operating profit for the third quarter of 2024 was
Net loss for the third quarter of 2024 was
Cash, cash equivalents, restricted cash and investments totaled
Financial Outlook for 2024
Based on the strength of patient demand for ORLADEYO seen in the third quarter, and expected continued strength in the fourth quarter, the company is adjusting its outlook for full year 2024 global net ORLADEYO revenue to be between
Directly related to the revenue strength for both ORLADEYO and RAPIVAB, the company is revising its guidance for operating expenses, and now expects full year 2024 operating expenses to be between
Based on the company’s disciplined approach to capital allocation, and the strong performance of ORLADEYO, the company is confident that it will achieve a full-year operating profit in 2024 (not including non-cash stock compensation), be approaching quarterly positive earnings per share (EPS) and positive cash flow in the second half of 2025 (not including non-cash stock compensation) and be profitable on an EPS basis, with positive cash flow, for full year 2026. The company expects it can achieve these financial milestones without raising additional funds.
Conference Call and Webcast
BioCryst management will host a conference call and webcast at 8:30 a.m. ET today to discuss the financial results and provide a corporate update. The live call may be accessed by dialing 1-844-481-2942 for domestic callers and 1-412-317-1866 for international callers. A live webcast and replay of the call will be available online in the investors section of the company website at www.biocryst.com.
About BioCryst Pharmaceuticals
BioCryst Pharmaceuticals is a global biotechnology company with a deep commitment to improving the lives of people living with hereditary angioedema and other rare diseases. BioCryst leverages its expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and protein therapeutics to target difficult-to-treat diseases. BioCryst has commercialized ORLADEYO® (berotralstat), the first oral, once-daily plasma kallikrein inhibitor, and is advancing a pipeline of small-molecule and protein therapies. For more information, please visit www.biocryst.com or follow us on LinkedIn.
Non-GAAP Financial Measures
The information furnished in this release includes non-GAAP financial measures that differ from measures calculated in accordance with generally accepted accounting principles in the United States of America (GAAP), including financial measures labeled as “non-GAAP” or “adjusted.”
We believe providing these non-GAAP measures, which show our results with these items adjusted, is valuable and useful since they allow management and investors to better understand the company’s financial performance in the absence of certain one-time events and non-cash items such as stock-based compensation and allow investors to more accurately understand our third quarter 2023 and 2024 and first nine months 2023 and 2024 results and more easily compare them to future results. These non-GAAP measures also correspond with the way we expected Wall Street analysts to compare our results. Our non-GAAP measures should be considered only as supplements to, and not as substitutes for or in isolation from, our other measures of financial information prepared in accordance with GAAP, such as GAAP revenue, operating income, net income, and earnings per share.
Our references to our first nine months 2023 “non-GAAP” financial measures of adjusted net loss and adjusted earnings per share constitute non-GAAP financial measures. They refer to our GAAP results, adjusted to show the results without the one-time loss on the extinguishment of the Athyrium term loans. Our references to our first nine months 2024 “non-GAAP” financial measures of adjusted net loss and adjusted earnings per share constitute non-GAAP financial measures. They refer to our GAAP results, adjusted to show the results without the one-time R&D restructuring expense. Our reference to our third quarter 2023 and 2024 and first nine months 2023 and 2024 “non-GAAP” financial measure of non-GAAP operating profit constitutes a non-GAAP financial measure. It refers to our GAAP results, adjusted to show the results without including non-cash stock compensation expense.
Forward-Looking Statements
This press release contains forward-looking statements, including statements regarding future results, performance or achievements. These statements involve known and unknown risks, uncertainties and other factors which may cause BioCryst’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These statements reflect our current views with respect to future events and are based on assumptions and are subject to risks and uncertainties. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Some of the factors that could affect the forward-looking statements contained herein include: BioCryst’s ability to successfully implement or maintain its commercialization plans for ORLADEYO; risks related to the planned discontinuation of the development of BCX10013; BioCryst’s ability to successfully progress its pipeline development plans as described herein; risks related to the reduction in size of BioCryst’s R&D organization; the results of BioCryst’s partnerships with third parties may not meet BioCryst’s current expectations; risks related to government actions, including that decisions and other actions, including as they relate to pricing, may not be taken when expected or at all, or that the outcomes of such decisions and other actions may not be in line with BioCryst’s current expectations; the commercial viability of ORLADEYO, including its ability to achieve sustained market acceptance and demand; ongoing and future preclinical and clinical development of product candidates may take longer than expected and may not have positive results; BioCryst may not be able to enroll the required number of subjects in planned clinical trials of product candidates; BioCryst may not advance human clinical trials with product candidates as expected; the FDA or other applicable regulatory agency may require additional studies beyond the studies planned for products and product candidates, may not provide regulatory clearances which may result in delay of planned clinical trials, may impose certain restrictions, warnings, or other requirements on products and product candidates, may impose a clinical hold with respect to product candidates, or may withhold, delay or withdraw market approval for products and product candidates; product candidates, if approved, may not achieve market acceptance; BioCryst’s ability to successfully commercialize its products and product candidates; BioCryst’s ability to successfully manage its growth and compete effectively; risks related to the international expansion of BioCryst’s business; timing for achieving and sustainability of profitability and positive cash flow may not meet management’s expectations; statements and projections regarding financial guidance and goals and the attainment of such goals may differ from actual results based on market factors and BioCryst’s ability to execute its operational and budget plans; and actual financial results may not be consistent with expectations, including that revenue, operating expenses and cash usage may not be within management’s expected ranges. Please refer to the documents BioCryst files periodically with the Securities and Exchange Commission, specifically BioCryst’s most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, and Current Reports on Form 8-K, which identify important factors that could cause actual results to differ materially from those contained in BioCryst’s projections and forward-looking statements.
BCRXW
Contact:
John Bluth
+1 919 859 7910
jbluth@biocryst.com
BIOCRYST PHARMACEUTICALS, INC. | |||||||||||||||
CONSOLIDATED FINANCIAL SUMMARY | |||||||||||||||
(In thousands, except per share) | |||||||||||||||
Statements of Operations (unaudited) | |||||||||||||||
Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
2024 | 2023 | 2024 | 2023 | ||||||||||||
Revenues: | |||||||||||||||
ORLADEYO | $ | 116,319 | $ | 85,684 | $ | 313,474 | $ | 235,107 | |||||||
Other | 766 | 1,058 | 5,704 | 2,904 | |||||||||||
Total revenues | 117,085 | 86,742 | 319,178 | 238,011 | |||||||||||
Expenses: | |||||||||||||||
Cost of product sales | 3,211 | 1,099 | 6,175 | 2,924 | |||||||||||
Research and development | 41,081 | 46,879 | 125,197 | 146,514 | |||||||||||
Selling, general and administrative | 65,084 | 50,648 | 185,662 | 149,512 | |||||||||||
Royalty | 17 | 37 | 179 | 100 | |||||||||||
Total operating expenses | 109,393 | 98,663 | 317,213 | 299,050 | |||||||||||
Income (loss) from operations | 7,692 | (11,921 | ) | 1,965 | (61,039 | ) | |||||||||
Interest income | 3,591 | 4,184 | 11,176 | 11,312 | |||||||||||
Interest expense | (24,828 | ) | (27,345 | ) | (74,067 | ) | (83,656 | ) | |||||||
Foreign currency gains (losses), net | 98 | (737 | ) | (37 | ) | (665 | ) | ||||||||
Loss on extinguishment of debt | — | — | — | (29,019 | ) | ||||||||||
Loss before income taxes | $ | (13,447 | ) | $ | (35,819 | ) | $ | (60,963 | ) | $ | (163,067 | ) | |||
Income tax expense | 586 | 330 | 1,123 | 1,741 | |||||||||||
Net loss | $ | (14,033 | ) | $ | (36,149 | ) | $ | (62,086 | ) | $ | (164,808 | ) | |||
Basic and diluted net loss per common share | $ | (0.07 | ) | $ | (0.19 | ) | $ | (0.30 | ) | $ | (0.87 | ) | |||
Weighted average shares outstanding | 206,905 | 189,644 | 206,466 | 189,095 |
Balance Sheet Data (in thousands) | |||||||
September 30, 2024 | December 31, 2023 | ||||||
(unaudited) | (Note 1) | ||||||
Cash, cash equivalents and investments | $ | 349,439 | $ | 388,987 | |||
Restricted cash | 2,223 | 1,804 | |||||
Receivables | 72,456 | 56,950 | |||||
Total assets | 491,254 | 516,960 | |||||
Secured term loan | 314,333 | 303,231 | |||||
Royalty financing obligation | 514,775 | 531,599 | |||||
Accumulated deficit | (1,743,245 | ) | (1,681,159 | ) | |||
Stockholders’ deficit | (468,563 | ) | (455,528 | ) | |||
Shares of common stock outstanding | 207,119 | 205,771 |
Note 1: Derived from audited financial statements.
Reconciliation of Adjusted Net Loss and Adjusted Diluted Earnings Per Share (in thousands) | |||||||||||||||
Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
2024 | 2023 | 2024 | 2023 | ||||||||||||
GAAP net loss | $ | (14,033 | ) | $ | (36,149 | ) | $ | (62,086 | ) | $ | (164,808 | ) | |||
Less: One-time R&D restructuring expense | — | — | (1,264 | ) | — | ||||||||||
Less: One-time loss on extinguishment of Athyrium term loans | — | — | — | (29,019 | ) | ||||||||||
Adjusted net loss | $ | (14,033 | ) | $ | (36,149 | ) | $ | (60,822 | ) | $ | (135,789 | ) | |||
GAAP basic and diluted net loss per common share | $ | (0.07 | ) | $ | (0.19 | ) | $ | (0.30 | ) | $ | (0.87 | ) | |||
Adjusted basic and diluted net loss per common share | $ | (0.07 | ) | $ | (0.19 | ) | $ | (0.29 | ) | $ | (0.72 | ) |
Reconciliation of Adjusted Income (Loss) from Operations (in thousands) | |||||||||||||||
Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
2024 | 2023 | 2024 | 2023 | ||||||||||||
GAAP income (loss) from operations | $ | 7,692 | $ | (11,921 | ) | $ | 1,965 | $ | (61,039 | ) | |||||
Less: Stock-based compensation expense | (17,249 | ) | (12,279 | ) | (44,074 | ) | (39,127 | ) | |||||||
Adjusted income (loss) from operations | $ | 24,941 | $ | 358 | $ | 46,039 | $ | (21,912 | ) |
FAQ
What was BCRX's ORLADEYO revenue in Q3 2024?
What is BioCryst's (BCRX) revenue guidance for ORLADEYO in 2024?
Did BCRX achieve profitability in Q3 2024?