Ardelyx Reports Second Quarter 2025 Financial Results and Provides Business Update
Rhea-AI Summary
Ardelyx (NASDAQ:ARDX) reported strong Q2 2025 financial results, with total revenue of $97.7 million, representing a 33% year-over-year growth. The company's flagship products showed significant performance: IBSRELA generated $65.0 million in net sales (84% YoY growth) and XPHOZAH contributed $25.0 million.
Key financial highlights include a strong cash position of $238.5 million as of June 30, 2025. The company raised its 2025 IBSRELA revenue guidance to $250-$260 million. Despite revenue growth, Ardelyx reported a net loss of $19.1 million ($0.08 per share) for Q2 2025.
Notable developments include securing an option to draw additional debt of $100 million through SLR Investment Corp. and key executive appointments including Mike Kelliher as Chief Business Officer and James P. Brady as Chief Human Resources Officer.
Positive
- Total revenue increased 33% year-over-year to $97.7 million
- IBSRELA sales grew 84% YoY to $65.0 million with increased guidance
- Strong cash position of $238.5 million
- Secured option for additional $100 million in debt financing
- XPHOZAH showed 27% quarter-over-quarter growth excluding one-time items
Negative
- Net loss increased to $19.1 million from $16.5 million YoY
- XPHOZAH revenue declined year-over-year due to Medicare coverage loss
- SG&A expenses increased 30% to $84.0 million
- R&D expenses increased 23% to $15.7 million
News Market Reaction 18 Alerts
On the day this news was published, ARDX gained 16.86%, reflecting a significant positive market reaction. Argus tracked a peak move of +10.0% during that session. Our momentum scanner triggered 18 alerts that day, indicating notable trading interest and price volatility. This price movement added approximately $189M to the company's valuation, bringing the market cap to $1.31B at that time.
Data tracked by StockTitan Argus on the day of publication.
Company reports strong commercial performance in the second quarter, recording
IBSRELA generated net sales revenue of
Company ends Q2 with
Company raises 2025 IBSRELA net sales revenue expectations to
Conference call scheduled for 4:30 PM Eastern Time
WALTHAM, Mass., Aug. 04, 2025 (GLOBE NEWSWIRE) -- Ardelyx, Inc. (Nasdaq: ARDX), a biopharmaceutical company founded with a mission to discover, develop and commercialize innovative, first-in-class medicines that meet significant unmet medical needs, today reported financial results for the second quarter ended June 30, 2025 and provided a business update.
“Ardelyx delivered an outstanding second quarter of 2025, generating nearly
Raab continued, “In addition to driving significant revenue growth, we carefully managed investments and closed on an option to draw additional debt at a reasonable cost. Ardelyx is gaining momentum as we head into the second half of 2025, and we remain focused on commercial execution and bringing our medicines to patients who need more options.”
IBSRELA® (tenapanor) records
IBSRELA reported
XPHOZAH® (tenapanor) records
U.S. net sales revenue for XPHOZAH during the second quarter of 2025 was
Other Corporate Developments
- In July, the company announced an amendment to its February 2022 loan agreement with investment affiliates managed by SLR Investment Corp. (SLR). The company drew the remaining
$50 million tranche at SOFR plus4% , subject to a SOFR floor of4.7% . The amendment also provides the Company with the option to draw an additional$100.0 million of debt, consisting of two tranches of$50.0 million . - In June, the company announced the appointment of Mike Kelliher as Chief Business Officer and James P. Brady as Chief Human Resources Officer.
- The company presented three posters, including results from the IBS in America 2024 supplemental survey demonstrating that the severity of IBS-C correlates with financial hardship and distress, at the 2025 Digestive Disease Week Conference, held May 3-6, 2025.
- The company presented a post-hoc analysis of the OPTIMIZE Study, an open-label clinical trial of XPHOZAH as a poster at the National Kidney Foundation 2025 Spring Clinical Meetings, held April 10-13, 2025.
Second Quarter 2025 Financial Results
• Cash Position: As of June 30, 2025, the company had total cash, cash equivalents and short-term investments of
• Revenues: Total revenue for the quarter ended June 30, 2025 was
- IBSRELA U.S. net product sales revenue was
$65.0 million , compared to$35.4 million during the same period of 2024. - XPHOZAH U.S. net product sales revenue was
$25.0 million , compared to$37.1 million during the same period of 2024. The year-over-year decline in revenue is due to the loss of Medicare coverage following the transition of oral only therapies into the Medicare End-Stage Renal Disease Prospective Payment System on January 1, 2025. - Product supply revenue was
$6.2 million , compared to$13 thousand during the same period of 2024. - Licensing revenue was
$20 thousand , compared to$19 thousand during the same period of 2024. - Non-cash royalty revenue related to the sale of future royalties was
$1.4 million , compared to$0.6 million during the same period of 2024.
• R&D Expenses: Research and development expenses were
• SG&A Expenses: Selling, general and administrative expenses were
• Net Loss: Net loss for the quarter ended June 30, 2025 was
Conference Call Details
The company will host a conference call today, August 4, 2025, at 4:30 PM ET to discuss today’s announcement. To participate in the conference call, please dial (877) 346-6112 (domestic) or (848) 280-6350 (international) and ask to be joined into the Ardelyx call. A webcast of the call can also be accessed by visiting the Investor page of the company's website, https://ir.ardelyx.com/, and will be available on the website for 30 days following the call.
IMPORTANT SAFETY INFORMATION (IBSRELA)
| WARNING: RISK OF SERIOUS DEHYDRATION IN PEDIATRIC PATIENTS IBSRELA is contraindicated in patients less than 6 years of age; in nonclinical studies in young juvenile rats administration of tenapanor caused deaths presumed to be due to dehydration. Avoid use of IBSRELA in patients 6 years to less than 12 years of age. The safety and effectiveness of IBSRELA have not been established in patients less than 18 years of age. |
CONTRAINDICATIONS
- IBSRELA is contraindicated in patients less than 6 years of age due to the risk of serious dehydration.
- IBSRELA is contraindicated in patients with known or suspected mechanical gastrointestinal obstruction.
WARNINGS AND PRECAUTIONS
Risk of Serious Dehydration in Pediatric Patients
- IBSRELA is contraindicated in patients below 6 years of age. The safety and effectiveness of IBSRELA in patients less than 18 years of age have not been established. In young juvenile rats (less than 1 week old; approximate human age equivalent of less than 2 years of age), decreased body weight and deaths occurred, presumed to be due to dehydration, following oral administration of tenapanor. There are no data available in older juvenile rats (human age equivalent 2 years to less than 12 years).
- Avoid the use of IBSRELA in patients 6 years to less than 12 years of age. Although there are no data in older juvenile rats, given the deaths in younger rats and the lack of clinical safety and efficacy data in pediatric patients, avoid the use of IBSRELA in patients 6 years to less than 12 years of age.
Diarrhea
Diarrhea was the most common adverse reaction in two randomized, double-blind, placebo-controlled trials of IBS-C. Severe diarrhea was reported in
MOST COMMON ADVERSE REACTIONS
The most common adverse reactions in IBSRELA-treated patients (incidence ≥
INDICATION
IBSRELA (tenapanor) is indicated for the treatment of Irritable Bowel Syndrome with Constipation (IBS-C) in adults.
Please see full Prescribing Information, including Boxed Warning, for additional risk information.
IMPORTANT SAFETY INFORMATION (XPHOZAH)
CONTRAINDICATIONS
XPHOZAH is contraindicated in:
- Pediatric patients under 6 years of age
- Patients with known or suspected mechanical gastrointestinal obstruction
WARNINGS AND PRECAUTIONS
Diarrhea
Patients may experience severe diarrhea. Treatment with XPHOZAH should be discontinued in patients who develop severe diarrhea.
MOST COMMON ADVERSE REACTIONS
Diarrhea, which occurred in 43
INDICATION
XPHOZAH (tenapanor), 30 mg BID, is indicated to reduce serum phosphorus in adults with chronic kidney disease (CKD) on dialysis as add-on therapy in patients who have an inadequate response to phosphate binders or who are intolerant of any dose of phosphate binder therapy.
For additional safety information, please see full Prescribing Information.
About Ardelyx
Ardelyx was founded with a mission to discover, develop and commercialize innovative, first-in-class medicines that meet significant unmet medical needs. Ardelyx has two commercial products approved in the United States, IBSRELA® (tenapanor) and XPHOZAH® (tenapanor) as well as early-stage pipeline candidates. Ardelyx has agreements for the development and commercialization of tenapanor outside of the U.S. Kyowa Kirin commercializes PHOZEVEL® (tenapanor) for hyperphosphatemia in Japan. A New Drug Application for tenapanor for hyperphosphatemia has been approved in China with Fosun Pharma. Knight Therapeutics commercializes IBSRELA in Canada. For more information, please visit https://ardelyx.com/ and connect with us on X (formerly known as Twitter), LinkedIn and Facebook.
Forward Looking Statements
To the extent that statements contained in this press release are not descriptions of historical facts regarding Ardelyx, they are forward-looking statements reflecting the current beliefs and expectations of management made pursuant to the safe harbor of the Private Securities Reform Act of 1995, including Ardelyx’s current expectations regarding the long term potential for Ardelyx’s existing commercial products; opportunities for continued IBSRELA and XPHOZAH net sales revenue growth during the remainder of 2025; and the projected U.S. net product sales revenue for IBSRELA for full year 2025. Such forward-looking statements involve known and unknown risks, uncertainties and other factors that are in some cases beyond our control, that could cause actual outcomes or results to differ materially from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, uncertainties associated with the development of, regulatory process for, and commercialization of drugs in the U.S. and internationally. Ardelyx undertakes no obligation to update or revise any forward-looking statements. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Ardelyx's business in general, please refer to Ardelyx's Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on August 4, 2025, and its future current and periodic reports to be filed with the Securities and Exchange Commission.
Investor and Media Contacts:
Caitlin Lowie
clowie@ardelyx.com
| Ardelyx, Inc. Condensed Balance Sheets (in thousands) | |||||||
| June 30, 2025 | December 31, 2024 | ||||||
| (Unaudited) | (1) | ||||||
| Assets | |||||||
| Cash and cash equivalents | $ | 90,045 | $ | 64,932 | |||
| Short-term investments | 148,407 | 185,168 | |||||
| Accounts receivable | 62,553 | 57,705 | |||||
| Prepaid commercial manufacturing | 12,740 | 16,378 | |||||
| Inventory | 123,259 | 91,184 | |||||
| Property and equipment, net | 2,143 | 1,495 | |||||
| Right-of-use assets | 5,006 | 2,380 | |||||
| Prepaid and other assets | 22,617 | 16,512 | |||||
| Total assets | $ | 466,770 | $ | 435,754 | |||
| Liabilities and stockholders’ equity | |||||||
| Accounts payable | $ | 21,685 | $ | 16,000 | |||
| Accrued compensation and benefits | 11,814 | 14,940 | |||||
| Current portion of operating lease liability | 1,182 | 1,562 | |||||
| Deferred revenue | 18,575 | 17,918 | |||||
| Accrued expenses and other liabilities | 44,776 | 35,665 | |||||
| Long-term debt | 201,446 | 150,853 | |||||
| Deferred royalty obligation related to the sale of future royalties | 27,761 | 25,527 | |||||
| Total stockholders’ equity | 139,531 | 173,289 | |||||
| Total liabilities and stockholders’ equity | $ | 466,770 | $ | 435,754 | |||
| (1) Derived from the audited financial statements included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2024. | |||||||
| Ardelyx, Inc. Condensed Statements of Operations (Unaudited) (in thousands, except share and per share amounts) | |||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| Revenues | |||||||||||||||
| Product sales, net | |||||||||||||||
| IBSRELA | $ | 65,045 | $ | 35,445 | $ | 109,448 | $ | 63,806 | |||||||
| XPHOZAH | 25,032 | 37,146 | 48,443 | 52,297 | |||||||||||
| Total product sales, net | 90,077 | 72,591 | 157,891 | 116,103 | |||||||||||
| Product supply revenue | 6,185 | 13 | 6,439 | 2,139 | |||||||||||
| Licensing revenue | 20 | 19 | 5,040 | 36 | |||||||||||
| Non-cash royalty revenue related to the sale of future royalties | 1,380 | 599 | 2,406 | 967 | |||||||||||
| Total revenues | 97,662 | 73,222 | 171,776 | 119,245 | |||||||||||
| Cost of goods sold | |||||||||||||||
| Cost of product sales | 3,245 | 1,405 | 5,585 | 2,418 | |||||||||||
| Other cost of revenue | 9,158 | 8,031 | 19,121 | 14,146 | |||||||||||
| Total cost of goods sold | 12,403 | 9,436 | 24,706 | 16,564 | |||||||||||
| Operating expenses | |||||||||||||||
| Research and development | 15,666 | 12,762 | 30,604 | 23,341 | |||||||||||
| Selling, general and administrative | 83,988 | 64,654 | 167,210 | 117,648 | |||||||||||
| Total operating expenses | 99,654 | 77,416 | 197,814 | 140,989 | |||||||||||
| Loss from operations | (14,395 | ) | (13,630 | ) | (50,744 | ) | (38,308 | ) | |||||||
| Interest expense | (4,356 | ) | (3,326 | ) | (8,547 | ) | (5,682 | ) | |||||||
| Non-cash interest expense related to the sale of future royalties | (2,219 | ) | (1,576 | ) | (4,290 | ) | (3,278 | ) | |||||||
| Other income, net | 1,892 | 2,145 | 4,218 | 4,484 | |||||||||||
| Loss before provision for income taxes | (19,078 | ) | (16,387 | ) | (59,363 | ) | (42,784 | ) | |||||||
| Provision for income taxes | 1 | 67 | 860 | 188 | |||||||||||
| Net loss | $ | (19,079 | ) | $ | (16,454 | ) | $ | (60,223 | ) | $ | (42,972 | ) | |||
| Net loss per share of common stock - basic and diluted | $ | (0.08 | ) | $ | (0.07 | ) | $ | (0.25 | ) | $ | (0.18 | ) | |||
| Shares used in computing net loss per share - basic and diluted | 239,928,570 | 234,571,192 | 239,279,962 | 233,818,576 | |||||||||||