IRVINE, Calif., Nov. 13, 2023 (GLOBE NEWSWIRE) -- Reneo Pharmaceuticals, Inc. (Nasdaq: RPHM), a clinical-stage pharmaceutical company focused on the development and commercialization of therapies for patients with rare genetic mitochondrial diseases, today reported financial results for the third quarter ended September 30, 2023 and provided a business update.
“We are looking forward to sharing topline results of our pivotal STRIDE study in December,” said Gregory J. Flesher, President and CEO of Reneo Pharmaceuticals. “In addition, we continue to be encouraged by the high participation rate in our STRIDE AHEAD open-label extension study, and are happy to announce enrollment of our first patient with PMM due to nuclear DNA defect in this ongoing trial. This is a very exciting time for the Reneo team and we want to thank our clinicians, patients, and stakeholders for supporting the mavodelpar development program.”
Third Quarter and Recent Highlights
Financial Results for the Three Months Ended September 30, 2023
We reported a net loss of $19.2 million, or $0.57 per share, during the third quarter of 2023, compared to a net loss of $13.0 million, or $0.53 per share, for the same period in 2022. We had $125.6 million in cash, cash equivalents, and short-term investments as of September 30, 2023.
Research and development (R&D) expenses were $13.6 million during the third quarter of 2023, compared to $9.9 million for the same period in 2022. This increase in R&D expenses was primarily due to an increase of $2.2 million related to clinical development and contract manufacturing costs to support the marketing registration for mavodelpar, an increase of $1.0 million in medical affairs costs, and an increase of $0.9 million in personnel-related costs due to additional headcount, offset by a decrease of $0.5 million of other R&D activities.
General and administrative (G&A) expenses were $7.3 million during the third quarter of 2023, compared to $3.9 million for the same period in 2022. This increase in G&A expenses was primarily due to an increase of $2.1 million in commercial development activities and an increase of $1.2 million in facility and personnel-related costs due to additional headcount.
About STRIDE
The STRIDE study is a global, randomized, double-blind, placebo-controlled pivotal Phase 2b trial of mavodelpar in adult patients with PMM due to mtDNA defects. The study is designed to investigate the efficacy and safety of 100 mg mavodelpar administered once-daily over a 24-week period. The primary efficacy endpoint of the trial is the change from baseline in the distance walked during the 12-minute walk test (12MWT) at week 24. Secondary and exploratory endpoints include changes from baseline in PROMIS® Short Form Fatigue 13a, Modified Fatigue Impact Scale (MFIS), Patient Global Impression of Change (PGIC), Patient Global Impression of Severity (PGIS), 30 Second Sit-To-Stand (30STS) Test, Brief Pain Inventory (BPI), 36-Item Health Survey (SF-36), Work Productivity and Activity Impairment Questionnaire: Specific Health Problem (WPAI:SHP), and Pedometer Step Count.
About STRIDE AHEAD
The STRIDE AHEAD study is an open-label extension (OLE) trial being conducted outside of the United States in patients with PMM due to mtDNA defects who participated in the STRIDE study or the mavodelpar Phase 1b study. The study is designed to evaluate the long-term safety and tolerability of 100 mg mavodelpar administered once-daily over a 24-month period. STRIDE AHEAD was amended to allow enrollment of treatment naïve patients with PMM due to nDNA defects.
About PMM
PMM are a group of rare, genetic metabolic disorders caused by mutations or deletions in the mtDNA or nDNA. These genetic alterations hamper the ability of mitochondria to generate energy from nutrient sources, resulting in energy deficits that are most pronounced in tissues with high energy demand such as muscle, brain, and heart. The symptoms of PMM include muscle weakness, exercise intolerance, movement disorder, deafness, blindness, and droopy eyelids among others. The prognosis for these disorders ranges in severity from progressive weakness to death.
About Mavodelpar
Mavodelpar (REN001) is a potent and selective peroxisome proliferator-activated receptor delta (PPARδ) agonist currently in clinical development for two rare genetic mitochondrial diseases that typically present with myopathy and have high unmet medical needs: PMM and long-chain fatty acid oxidation disorder. For additional information, please see clinicaltrials.gov.
About Reneo Pharmaceuticals
Reneo is a clinical-stage pharmaceutical company focused on the development and commercialization of therapies for patients with rare genetic mitochondrial diseases, which are often associated with the inability of mitochondria to produce adenosine triphosphate (ATP). Our lead product candidate, mavodelpar (REN001), is a potent and selective agonist of the peroxisome proliferator-activated receptor delta (PPARδ). Mavodelpar has been shown to increase transcription of genes involved in mitochondrial function, increase fatty acid oxidation, and may increase production of new mitochondria. For additional information, please see reneopharma.com.
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the potential development, registration and commercialization of mavodelpar, the timing of topline results from the STRIDE study and the anticipated expiration for patent applications. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as “plans,” “will,” “believes,” “anticipates,” “expects,” “intends,” “goal,” “potential” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Reneo’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Reneo’s business in general, and the other risks described in Reneo’s filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made. Reneo undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.
| RENEO PHARMACEUTICALS, INC. Consolidated Balance Sheets (In thousands, except share and par value data) | ||||||||
| September 30, 2023 | December 31, 2022 | |||||||
| (Unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 11,737 | $ | 19,927 | ||||
| Short-term investments | 113,877 | 81,246 | ||||||
| Prepaid expenses and other current assets | 3,158 | 5,180 | ||||||
| Total current assets | 128,772 | 106,353 | ||||||
| Property and equipment, net | 529 | 453 | ||||||
| Right-of-use assets | 1,006 | 1,292 | ||||||
| Other non-current assets | 81 | 84 | ||||||
| Total assets | $ | 130,388 | $ | 108,182 | ||||
| Liabilities and stockholders’ equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 2,473 | $ | 1,893 | ||||
| Accrued expenses | 10,765 | 4,827 | ||||||
| Operating lease liabilities, current portion | 325 | 404 | ||||||
| Total current liabilities | 13,563 | 7,124 | ||||||
| Operating lease liabilities, less current portion | 812 | 1,059 | ||||||
| Performance award | 1,069 | 29 | ||||||
| Total liabilities | 15,444 | 8,212 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders’ equity: | ||||||||
| Common stock, $0.0001 par value; 200,000,000 shares authorized at September 30, 2023 and December 31, 2022; 33,872,166 and 24,699,553 shares issued and outstanding at September 30, 2023 and December 31, 2022, respectively | 3 | 3 | ||||||
| Additional paid-in capital | 305,479 | 236,693 | ||||||
| Accumulated deficit | (190,517 | ) | (136,683 | ) | ||||
| Accumulated other comprehensive loss | (21 | ) | (43 | ) | ||||
| Total stockholders’ equity | 114,944 | 99,970 | ||||||
| Total liabilities and stockholders’ equity | $ | 130,388 | $ | 108,182 | ||||
| RENEO PHARMACEUTICALS, INC. Consolidated Statements of Operations and Comprehensive Loss (In thousands, except share and per share data) (Unaudited) | ||||||||||||||||
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | $ | 13,622 | $ | 9,938 | $ | 39,009 | $ | 27,348 | ||||||||
| General and administrative | 7,266 | 3,902 | 19,038 | 11,938 | ||||||||||||
| Total operating expenses | 20,888 | 13,840 | 58,047 | 39,286 | ||||||||||||
| Loss from operations | (20,888 | ) | (13,840 | ) | (58,047 | ) | (39,286 | ) | ||||||||
| Other income | 1,692 | 833 | 4,213 | 931 | ||||||||||||
| Net loss | (19,196 | ) | (13,007 | ) | (53,834 | ) | (38,355 | ) | ||||||||
| Unrealized gain (loss) on short-term investments | 10 | (194 | ) | 22 | (60 | ) | ||||||||||
| Comprehensive loss | $ | (19,186 | ) | $ | (13,201 | ) | $ | (53,812 | ) | $ | (38,415 | ) | ||||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.57 | ) | $ | (0.53 | ) | $ | (1.81 | ) | $ | (1.57 | ) | ||||
| Weighted-average shares used in computing net loss per share, basic and diluted | 33,807,945 | 24,496,313 | 29,718,689 | 24,472,974 | ||||||||||||
| RENEO PHARMACEUTICALS, INC. Consolidated Statements of Cash Flows (In thousands) (Unaudited) | ||||||||
| Nine Months Ended September 30, | ||||||||
| 2023 | 2022 | |||||||
| Cash flows from operating activities | ||||||||
| Net loss | $ | (53,834 | ) | $ | (38,355 | ) | ||
| Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
| Stock-based compensation | 3,793 | 3,103 | ||||||
| Depreciation and amortization | 126 | 63 | ||||||
| Amortization/accretion on short-term investments | (3,551 | ) | (169 | ) | ||||
| Changes in the fair value of performance award | 1,040 | (378 | ) | |||||
| Non-cash lease expense | 354 | 338 | ||||||
| Loss on disposal of fixed asset | 5 | 3 | ||||||
| Changes in operating assets and liabilities: | ||||||||
| Prepaid expenses and other assets | 2,025 | 1,146 | ||||||
| Accounts payable and accrued expenses | 6,507 | 2,838 | ||||||
| Operating lease liabilities | (394 | ) | (338 | ) | ||||
| Net cash used in operating activities | (43,929 | ) | (31,749 | ) | ||||
| Cash flows from investing activities | ||||||||
| Purchases of property and equipment | (196 | ) | (96 | ) | ||||
| Purchase of available-for-sale short-term investments | (190,058 | ) | (67,329 | ) | ||||
| Proceeds from maturities of available-for-sale short-term investments | 161,000 | 36,500 | ||||||
| Net cash used in by investing activities | (29,254 | ) | (30,925 | ) | ||||
| Cash flows from financing activities | ||||||||
| Proceeds from public offering of common stock, net of offering costs | 58,862 | — | ||||||
| Proceeds from private placement of common stock, net of offering costs | 4,667 | — | ||||||
| Proceeds from issuance of common stock under the at-the-market facility, net of offering costs | 1,009 | — | ||||||
| Proceeds from issuance of common stock in connection with equity plans | 455 | 146 | ||||||
| Net cash provided by financing activities | 64,993 | 146 | ||||||
| Net decrease in cash and cash equivalents | (8,190 | ) | (62,528 | ) | ||||
| Cash and cash equivalents, beginning of period | 19,927 | 124,660 | ||||||
| Cash and cash equivalents, end of period | $ | 11,737 | $ | 62,132 | ||||
| Noncash operating activities: | ||||||||
| Right-of-use assets obtained in exchange for lease obligations | $ | — | $ | 1,524 | ||||
| Noncash investing and financing activities: | ||||||||
| Property and equipment in accounts payable | $ | 11 | $ | — | ||||
Contacts:
Danielle Spangler
Investor Relations
Reneo Pharmaceuticals, Inc.
This email address is being protected from spambots. You need JavaScript enabled to view it.
Matthew Purcell
Media Inquiries
Russo Partners, LLC
This email address is being protected from spambots. You need JavaScript enabled to view it.
| Last Trade: | US$1.82 |
| Daily Volume: | 0 |
| Market Cap: | US$60.840M |
October 04, 2024 March 28, 2024 | |
Northstar Clean Technologies is a cleantech company focused on the sustainable recovery and reprocessing of asphalt shingles. Northstar’s mission is to be the leader in the recovery and reprocessing of asphalt shingles in North America...
CLICK TO LEARN MORE
Surf Air Mobility is a regional air mobility platform expanding the category of regional air travel to reinvent flying through the power of electrification. In an effort to substantially reduce the cost and environmental impact of...
CLICK TO LEARN MORE
