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Reneo Pharmaceuticals Reports Second Quarter 2022 Financial Results

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Reneo Pharmaceuticals (RPHM) reported its Q2 2022 financial results, highlighting a net loss of $12.3 million, or $0.50 per share, compared to a loss of $9.2 million, or $0.43 per share in Q2 2021. The company achieved significant progress in its mitochondrial disease programs, including positive results from the REN001 long-chain fatty acid oxidation disorders study and advancements in the STRIDE study for primary mitochondrial myopathies, with two-thirds enrollment completed. Cash and equivalents stood at approximately $127 million as of June 30, 2022.

Positive
  • Positive results reported from the REN001 Phase 1b long-chain fatty acid oxidation disorders study.
  • Two-thirds enrollment achieved in the pivotal STRIDE study for primary mitochondrial myopathies.
  • Plans to initiate a third REN001 program for patients with nuclear DNA defects.
  • Strong cash position with approximately $127 million available.
Negative
  • Net loss increased to $12.3 million for Q2 2022 from $9.2 million in Q2 2021.
  • R&D expenses rose to $8.1 million, up from $6.3 million in the previous year.

IRVINE, Calif., Aug. 09, 2022 (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 quarter ended June 30, 2022.

“The second quarter was a very productive period for the company, highlighted by advancements in both of our mitochondrial disease programs,” said Gregory J. Flesher, President and CEO of Reneo Pharmaceuticals. “We recently reported positive results from the REN001 long-chain fatty acid oxidation disorders study, and look forward to meeting with regulators to discuss next steps for this program. In addition, we continued to make good progress with our primary mitochondrial myopathies program, including achievement of two-thirds enrollment in the pivotal STRIDE study, gaining alignment on the planned registration plan in Europe, and announcing plans to begin a third development program in patients with nuclear DNA defects.”

Second Quarter and Recent Highlights

  • Published REN001 Phase 1 leg-immobilization study in the Journal of Clinical Trials (Link)
  • Reported positive results from REN001 Phase 1b long-chain fatty acid oxidation disorders (LC-FAOD) study
  • Announced plans to initiate a third REN001 program in primary mitochondrial myopathies (PMM) patients with nuclear DNA (nDNA) defects
  • Appointed Roshawn Blunt to the Board of Directors

Anticipated Milestones

  • Presentation of LC-FAOD studies at the International Network for Fatty Acid Oxidation Research and Management (INFORM) Conference, Aug 28-29 (Freiburg, Germany)
  • Completion of enrollment in the pivotal STRIDE study, year-end 2022
  • Meetings with regulatory agencies to discuss LC-FAOD and nDNA PMM programs, 4Q22/1Q23

Financial Results for the Three Months Ended June 30, 2022

The Company reported a net loss of $12.3 million, or $0.50 per share, for the three months ended June 30, 2022, compared to a net loss of $9.2 million, or $0.43 per share, for the three months ended June 30, 2021. The Company had approximately $127 million in cash, cash equivalents and short-term investments as of June 30, 2022.

Research and development expenses for the three months ended June 30, 2022 were $8.1 million, compared to $6.3 million for the three months ended June 30, 2021. This increase of $1.8 million was primarily due to a $1.1 million increase in personnel-related costs due to the additional headcount required to support our clinical and manufacturing operations. In addition, there was a $0.4 million increase in clinical trial and manufacturing costs and a $0.4 million increase in non-clinical activities.

General and administrative expenses for the three months ended June 30, 2022 were $4.3 million, compared to $2.9 million during the three months ended June 30, 2021. This increase of $1.4 million was primarily attributable to increased costs to operate as a public company, including increases in outside professional services of $1.1 million and personnel-related expenses of $0.1 million.

Corporate Access Events

  • Baird Global Healthcare Conference, Sep 13-14 (New York)
  • Landenburg Thalmann Annual Healthcare Conference, Sep 29 (New York)
  • Piper Sandler Annual Healthcare Conference, Nov 29 – Dec 1 (New York)

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, REN001, is a potent and selective agonist of the peroxisome proliferator-activated receptor delta (PPARδ). REN001 has been shown to increase transcription of genes involved in mitochondrial function and increase fatty acid oxidation, and may increase production of new mitochondria. For additional information, please see reneopharma.com.

About REN001

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 LC-FAOD. For additional information, please see clinicaltrials.gov.

About PMM

PMM are a group of disorders caused by genetic mutations within the mitochondrial DNA or nDNA that affect the activity of enzymes or other proteins in the mitochondria. In PMM 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 or 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 LC-FAOD

LC-FAOD are a group of rare genetic metabolic disorders caused by mutations or deletions in the nDNA. These genetic alterations prevent the body from breaking down long-chain fatty acids during metabolism. The most severe cases of LC-FAOD are diagnosed within the first few days or weeks of life. Young patients often present with a severe energy deficit that results in lethargy, liver dysfunction, hypoglycemia, encephalopathy, and high risk for sudden death. Older patients usually present with muscle weakness, exercise intolerance, muscle aches, or rhabdomyolysis which can damage the heart and kidneys and cause permanent disability or even death.

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 and commercialization of REN001, results, conduct, progress, plans and timing of Reneo’s clinical studies, including the planned registration plan in Europe, presentation of data from clinical trials, meetings with regulatory agencies and the regulatory approval path for REN001. 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)

  June 30,
2022
  December 31,
2021
 
  (Unaudited)    
Assets      
Current assets:      
Cash and cash equivalents $118,264  $124,660 
Short-term investments  8,588   23,010 
Prepaid expenses and other current assets  5,159   6,064 
Total current assets  132,011   153,734 
Property and equipment, net  236   212 
Right-of-use assets  1,283    
Other non-current assets  78   78 
Total assets $133,608  $154,024 
Liabilities and stockholders’ equity      
Current liabilities:      
Accounts payable $1,560  $2,022 
Accrued expenses  6,367   4,180 
Operating lease liabilities, current portion  408    
Total current liabilities  8,335   6,202 
Operating lease liabilities, less current portion  1,061    
Other long-term liabilities     167 
Performance award  55   444 
Total liabilities  9,451   6,813 
Commitments and contingencies      
Stockholders’ equity:      
Common stock, $0.0001 par value; 200,000,000 shares authorized at June 30, 2022 and
December 31, 2021; 24,479,646 shares issued and outstanding at June 30, 2022; and
24,457,838 and 24,455,390 shares issued and outstanding at December 31, 2021, respectively
  3   3 
Additional paid-in capital  234,062   231,902 
Accumulated deficit  (110,076)  (84,728)
Accumulated other comprehensive income  168   34 
Total stockholders’ equity  124,157   147,211 
Total liabilities and stockholders’ equity $133,608  $154,024 
         

RENEO PHARMACEUTICALS, INC.
Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
(Unaudited)

  Three Months Ended June 30,  Six Months Ended June 30, 
  2022  2021  2022  2021 
Operating expenses:            
Research and development $8,132  $6,279  $17,410  $11,751 
General and administrative  4,299   2,949   8,036   4,691 
Total operating expenses  12,431   9,228   25,446   16,442 
Loss from operations  (12,431)  (9,228)  (25,446)  (16,442)
Other income  119   12   98   14 
Net loss  (12,312)  (9,216)  (25,348)  (16,428)
Unrealized gain on short-term investments  104   5   134   5 
Comprehensive loss $(12,208) $(9,211) $(25,214) $(16,423)
Net loss per share attributable to common stockholders, basic and diluted $(0.50) $(0.43) $(1.04) $(1.40)
Weighted-average shares used in computing net loss per share, basic and diluted  24,463,824   21,364,369   24,461,085   11,770,948 
                 

RENEO PHARMACEUTICALS, INC.
Consolidated Statements of Cash Flows
(In thousands)
(Unaudited)

  Six Months Ended
June 30,
 
  2022  2021 
Cash flows from operating activities      
Net loss $(25,348) $(16,428)
Adjustments to reconcile net loss to net cash used in operating activities:      
Stock-based compensation  2,113   1,325 
Depreciation and amortization  41   20 
Amortization/accretion on short-term investments  (22)  33 
Changes in the fair value of performance award  (389)  363 
Non-cash lease expense  241    
Changes in operating assets and liabilities:      
Prepaid expenses and other assets  905   (2,457)
Accounts payable and accrued expenses  1,726   (1,164)
Operating lease liabilities  (222)   
Other current and long-term liabilities     18 
Net cash used in operating activities  (20,955)  (18,290)
Cash flows from investing activities      
Purchases of property and equipment  (68)  (31)
Purchase of available-for-sale short-term investments  (15,922)  (26,989)
Proceeds from maturities of available-for-sale short-term investments  30,500    
Net cash provided by (used in) investing activities  14,510   (27,020)
Cash flows from financing activities      
Proceeds from issuance of Series B convertible preferred stock, net of issuance costs     47,239 
Proceeds from initial public offering, net of offering costs     84,639 
Proceeds from issuance of common stock in connection with equity plans  49   187 
Net cash provided by financing activities  49   132,065 
Net (decrease) increase in cash and cash equivalents  (6,396)  86,755 
Cash and cash equivalents, beginning of period  124,660   53,613 
Cash and cash equivalents, end of period $118,264  $140,368 
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 $  $10 
Accrued deferred initial public offering costs $  $30 
         

Contacts:

Joyce Allaire
Managing Director
LifeSci Advisors, LLC
jallaire@lifesciadvisors.com

Danielle Spangler
Investor Relations
Reneo Pharmaceuticals, Inc.
dspangler@reneopharma.com


FAQ

What were Reneo Pharmaceuticals' financial results for Q2 2022?

Reneo Pharmaceuticals reported a net loss of $12.3 million, or $0.50 per share, for Q2 2022.

What progress did Reneo Pharmaceuticals make in its clinical programs?

Reneo Pharmaceuticals reported significant advancements in its mitochondrial disease programs, including positive results from the REN001 study and two-thirds enrollment in the STRIDE study.

How much cash does Reneo Pharmaceuticals have as of June 30, 2022?

As of June 30, 2022, Reneo Pharmaceuticals had approximately $127 million in cash, cash equivalents, and short-term investments.

What are the anticipated milestones for Reneo Pharmaceuticals?

Reneo Pharmaceuticals anticipates presenting LC-FAOD studies at the INFORM Conference in August 2022 and completing enrollment in the STRIDE study by the end of 2022.

What were the R&D expenses for Reneo Pharmaceuticals in Q2 2022?

R&D expenses for Q2 2022 were $8.1 million, an increase from $6.3 million in Q2 2021.

Reneo Pharmaceuticals, Inc.

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