Agios Reports Business Highlights and First Quarter 2024 Financial Results
Agios Pharmaceuticals, Inc. reported positive results from the Phase 3 ENERGIZE study of mitapivat in thalassemia. Mitapivat has potential as the first approved therapy for all thalassemia subtypes. The company posted $8.2 million in net revenue for PYRUKYND® in Q1 2024. Agios also disclosed upcoming milestones in sickle cell disease, pediatric PK deficiency, and lower-risk Myelodysplastic Syndromes. Financially, the company had $714.3 million in cash, cash equivalents, and marketable securities as of March 31, 2024. Agios aims to fund operations until at least 2026.
Positive data from Phase 3 ENERGIZE study of mitapivat in thalassemia.
Successful net revenue of $8.2 million for PYRUKYND® in Q1 2024.
Potential for mitapivat to be the first approved therapy for all thalassemia subtypes.
Upcoming milestones in sickle cell disease, pediatric PK deficiency, and lower-risk Myelodysplastic Syndromes.
Strong financial position with $714.3 million in cash, cash equivalents, and marketable securities as of March 31, 2024.
Increased R&D expenses of $68.6 million in Q1 2024 compared to $67.3 million in Q1 2023.
Net loss of $81.5 million in Q1 2024 compared to $81.0 million in Q1 2023.
Cash, cash equivalents, and marketable securities decreased to $714.3 million as of March 31, 2024, from $806.4 million as of December 31, 2023.
Insights
The 15 percent sequential increase in PYRUKYND® net revenue to
Agios’ cash and securities position of
Agios Pharmaceuticals' focus on mitapivat as a potential first-in-class therapy for thalassemia could signify a significant milestone for the company and patients. Positive results from the Phase 3 ENERGIZE study and anticipated topline data from the ENERGIZE-T study in transfusion-dependent thalassemia could pave the way for FDA approval. These developments may not only broaden the drug's market but could also be a strong catalyst for the company's valuation.
Looking further ahead, the initiation of the Phase 1 study of AG-181 for phenylketonuria (PKU) showcases Agios' commitment to expanding its pipeline within the rare disease space. The evolution from a single-product company to one with multiple assets in development or on the market is a critical driver of growth and investor confidence in the biotech sector.
Agios’ strategic retention of economic rights to vorasidenib, with a potential
– Topline Data Readout from the Phase 3 ENERGIZE-T Study of Mitapivat in Adults with Transfusion-Dependent Alpha- or Beta-Thalassemia now expected in Q2 2024 –
– Announced Positive Results from the Phase 3 ENERGIZE Study of Mitapivat in Adults with Non-Transfusion-Dependent Alpha- or Beta-Thalassemia in January –
– Phase 3 Readouts from Mitapivat RISE UP Study in Sickle Cell Disease, ACTIVATE-KIDS and ACTIVATE KIDS-T in Pediatric PK Deficiency, All Expected by End of 2025 –
– PYRUKYND® (Mitapivat) Net Revenue of
CAMBRIDGE, Mass., May 02, 2024 (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a leader in cellular metabolism and PK activation pioneering therapies for rare diseases, today reported business highlights and financial results for the first quarter ended March 31, 2024.
“We were delighted to report positive data from the Phase 3 ENERGIZE study of mitapivat in non-transfusion-dependent thalassemia and look forward to announcing topline data from the Phase 3 ENERGIZE-T study in transfusion-dependent thalassemia in the second quarter of this year,” said Brian Goff, chief executive officer at Agios. “Mitapivat has the potential to become the first therapy approved for all thalassemia subtypes, and our commercial organization is actively preparing for a potential launch next year. Beyond thalassemia, we look forward to the RISE UP Phase 3 readout in sickle cell disease next year, with potential for approval in 2026, as we progress toward our vision of becoming a leading rare disease company with a potential multi-billion-dollar franchise in PK activation.”
First Quarter 2024 and Recent Highlights
- PYRUKYND® Revenues: Generated
$8.2 million in net revenue for the first quarter of 2024, a 15 percent sequential increase from the fourth quarter of 2023, primarily driven by increased patient demand. A total of 188 unique patients have completed prescription enrollment forms, representing an increase of 6 percent over the fourth quarter of 2023. A total of 120 patients are on PYRUKYND® therapy, a 10 percent increase from the fourth quarter of 2023. - Thalassemia: Announced positive results from the Phase 3 ENERGIZE study of mitapivat in adults with non-transfusion-dependent alpha- or beta-thalassemia.
- Earlier-Stage Pipeline: Dosed the first participants in the Phase 1 study of AG-181 for the treatment of phenylketonuria (PKU).
- Environment, Social, and Governance (ESG): Published 2024 ESG Report, which provides corporate sustainability disclosures for the period Jan. 1, 2023 to Dec. 31, 2023.
- Other: Servier announced FDA filing acceptance and priority review for a new drug application (NDA) for vorasidenib for the treatment of IDH-mutant diffuse glioma. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) action date of August 20, 2024. As part of the divestiture of Agios’ oncology business to Servier, Agios retains rights to a potential
$200 million milestone upon FDA approval of vorasidenib and15% royalties on potential U.S. net sales.
Key Upcoming Milestones & Priorities
Agios expects to execute on the following additional key milestones and priorities by the end of 2024:
- Thalassemia: Two key milestones for the year, including reporting topline data from the Phase 3 ENERGIZE-T study of mitapivat in transfusion-dependent thalassemia (Q2) and filing for FDA approval of mitapivat in thalassemia (year-end).
- Sickle Cell Disease: Complete enrollment in the Phase 3 portion of the RISE UP study of mitapivat (year-end).
- Pediatric PK Deficiency: Complete enrollment in the Phase 3 ACTIVATE-kids study of mitapivat (mid-year). Report topline data from Phase 3 ACTIVATE kids-T study (now mid-year).
- Lower-risk Myelodysplastic Syndromes: Dose first patient in Phase 2b study of AG-946 (mid-year).
- Other: Potential approval of Servier’s vorasidenib for the treatment of IDH-mutant diffuse glioma. The FDA has assigned a PDUFA action date of August 20, 2024. Agios retains certain economic rights, as described above.
First Quarter 2024 Financial Results
Revenue: Net product revenue from sales of PYRUKYND® for the first quarter of 2024 was
Cost of Sales: Cost of sales for the first quarter of 2024 was
Research and Development (R&D) Expenses: R&D expenses were
Selling, General and Administrative (SG&A) Expenses: SG&A expenses were
Net Loss: Net loss was
Cash Position and Guidance: Cash, cash equivalents and marketable securities as of March 31, 2024, were
Conference Call Information
Agios will host a conference call and live webcast with slides today at 8:00 a.m. ET to discuss first quarter 2024 financial results and recent business highlights. The live webcast can be accessed under “Events & Presentations” in the Investors section of the company’s website at www.agios.com. The archived webcast will be available on the company's website beginning approximately two hours after the event.
About Agios
Agios is the pioneering leader in PK activation and is dedicated to developing and delivering transformative therapies for patients living with rare diseases. In the U.S., Agios markets a first-in-class pyruvate kinase (PK) activator for adults with PK deficiency, the first disease-modifying therapy for this rare, lifelong, debilitating hemolytic anemia. Building on the company's deep scientific expertise in classical hematology and leadership in the field of cellular metabolism and rare hematologic diseases, Agios is advancing a robust clinical pipeline of investigational medicines with programs in alpha- and beta-thalassemia, sickle cell disease, pediatric PK deficiency, MDS-associated anemia and phenylketonuria (PKU). In addition to its clinical pipeline, Agios is advancing a preclinical TMPRSS6 siRNA as a potential treatment for polycythemia vera. For more information, please visit the company’s website at www.agios.com.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Such forward-looking statements include those regarding the potential benefits of PYRUKYND® (mitapivat), AG-946, TMPRSS6 siRNA and AG-181, Agios’ PAH stabilizer; Agios’ plans, strategies and expectations for its preclinical, clinical and commercial advancement of its drug development, including PYRUKYND®, AG-946 and AG-181, its PAH stabilizer; Agios’ strategic vision and goals, including its key milestones for 2024; and the potential benefits of Agios’ strategic plans and focus. The words “anticipate,” “expect,” “goal,” “hope,” “milestone,” “plan,” “potential,” “possible,” “strategy,” “will,” “vision,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Such statements are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from Agios’ current expectations and beliefs. For example, there can be no guarantee that any product candidate Agios is developing will successfully commence or complete necessary preclinical and clinical development phases, or that development of any of Agios’ product candidates will successfully continue. There can be no guarantee that any positive developments in Agios’ business will result in stock price appreciation. Management's expectations and, therefore, any forward-looking statements in this press release could also be affected by risks and uncertainties relating to a number of other important factors, including, without limitation: risks and uncertainties related to the impact of pandemics or other public health emergencies to Agios’ business, operations, strategy, goals and anticipated milestones, including its ongoing and planned research activities, ability to conduct ongoing and planned clinical trials, clinical supply of current or future drug candidates, commercial supply of current or future approved products, and launching, marketing and selling current or future approved products; Agios’ results of clinical trials and preclinical studies, including subsequent analysis of existing data and new data received from ongoing and future studies; the content and timing of decisions made by the U.S. FDA, the EMA or other regulatory authorities, investigational review boards at clinical trial sites and publication review bodies; Agios’ ability to obtain and maintain requisite regulatory approvals and to enroll patients in its planned clinical trials; unplanned cash requirements and expenditures; competitive factors; Agios' ability to obtain, maintain and enforce patent and other intellectual property protection for any product candidates it is developing; Agios’ ability to establish and maintain key collaborations; uncertainty regarding any milestone or royalty payments related to the sale of its oncology business or its in-licensing of TMPRSS6 siRNA, and the uncertainty of the timing of any such payments; uncertainty of the results and effectiveness of the use of Agios’ cash and cash equivalents; and general economic and market conditions. These and other risks are described in greater detail under the caption "Risk Factors" included in Agios’ public filings with the Securities and Exchange Commission. Any forward-looking statements contained in this press release speak only as of the date hereof, and Agios expressly disclaims any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.
| Consolidated Balance Sheet Data | |||||||
| (in thousands) | |||||||
| (Unaudited) | |||||||
| March 31, 2024 | December 31, 2023 | ||||||
| Cash, cash equivalents, and marketable securities | $ | 714,292 | $ | 806,363 | |||
| Accounts receivable, net | 3,453 | 2,810 | |||||
| Inventory | 23,070 | 19,076 | |||||
| Total assets | 849,709 | 937,118 | |||||
| Stockholders' equity | 743,922 | 811,019 | |||||
| Consolidated Statements of Operations Data | |||||||
| (in thousands, except share and per share data) | |||||||
| (Unaudited) | |||||||
| Three Months Ended March 31, | |||||||
| 2024 | 2023 | ||||||
| Revenues: | |||||||
| Product revenue, net | $ | 8,189 | $ | 5,609 | |||
| Total revenue | 8,189 | 5,609 | |||||
| Operating expenses: | |||||||
| Cost of sales | $ | 627 | $ | 554 | |||
| Research and development | 68,620 | 67,301 | |||||
| Selling, general and administrative | 31,014 | 28,367 | |||||
| Total operating expenses | 100,261 | 96,222 | |||||
| Loss from operations | (92,072 | ) | (90,613 | ) | |||
| Interest income, net | 8,889 | 8,091 | |||||
| Other income, net | 1,634 | 1,504 | |||||
| Net loss | $ | (81,549 | ) | $ | (81,018 | ) | |
| Net loss per share - basic and diluted | $ | (1.45 | ) | $ | (1.47 | ) | |
| Weighted-average number of common shares used in computing net loss per share – basic and diluted | 56,383,475 | 55,265,390 | |||||
Contacts:
Investor Contact
Chris Taylor, VP Investor Relations and Corporate Communications
Agios Pharmaceuticals
IR@agios.com
Media Contact
Dan Budwick
1AB
dan@1abmedia.com
FAQ
What were the net revenues reported for PYRUKYND® in Q1 2024?
What Phase 3 study did Agios announce positive results for in adults with non-transfusion-dependent thalassemia?
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What are some upcoming milestones for Agios by the end of 2024?
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