Catalyst Pharmaceuticals Reports Strong Third Quarter 2023 Financial Results and Corporate Update

  • Third Quarter 2023 Total Net Revenues of $102.7 Million, a 79.4% Increase YOY
  • Third Quarter 2023 GAAP Net Loss per Share of $(0.29) Diluted, Impacted by an $81.5 Million One Time Non-Recurring IPR&D Expense Related to the Acquisition of AGAMREE® License
  • Third Quarter 2023 Non-GAAP Net Income of $55.9 Million, $0.49 per Share Diluted
  • Reported U.S. FDA Approval of AGAMREE® (vamorolone) for Duchenne Muscular Dystrophy
  • sNDA Seeking to Increase FIRDAPSE® Maximum Daily Dose to 100 mg Accepted for Filing by the FDA
  • Two New FIRDAPSE Patents Have Recently been Allowed; Upon Issuance will be Posted to the FDA's Orange Book, Further Strengthening our Intellectual Property Portfolio
  • Raising Full Year 2023 Total Revenue Guidance to Between $390 Million and $395 Million
  • Conference Call and Webcast to be Held on November 9, 2023, at 8:30 AM ET

CORAL GABLES, Fla., Nov. 08, 2023 (GLOBE NEWSWIRE) -- Catalyst Pharmaceuticals, Inc. ("Catalyst" or "the Company") (Nasdaq: CPRX) today reported financial results for the third quarter of 2023 and provided a corporate update.

"Our strong results in the third quarter reflect our exceptional strategic execution and substantial investment in assisting the physician community to better identify and treat LEMS patients with and without small-cell lung cancer. Our quarterly results were exceptional, having attained several significant milestones that have transformed the long-term growth trajectory of our Company," stated Patrick J. McEnany, Catalyst's Chairman and CEO. "We are working diligently in preparation for the commercial launch of AGAMREE® during the first quarter of 2024. We are pleased to be able to provide AGAMREE to the DMD community, many who have been anxiously awaiting the availability of a steroid with a favorable safety profile. Our highly skilled and experienced neuromuscular commercial and medical affairs teams will be ready to hit the ground running for the commercial launch of AGAMREE. As we look ahead to the coming year, we are confident in our ability to execute our strategic plans, laying the foundation for continued growth and sustained progress."

Financial Highlights (in Millions of U.S. dollars, except per share data, unaudited)

For the Three Months Ended September 30,   2023     2022   % Change
Total Net Product Revenues $ 102,617   $ 57,173   79.5 %
FIRDAPSE Net Product Revenues $ 66,224   $ 57,173   15.8 %
FYCOMPA Net Product Revenues $ 36,393     N/A   N/A  
GAAP Net Income (Loss) $ (30,764 ) $ 22,748   (235.2 )%
Non-GAAP Net Income ** $ 55,870   $ 28,615   95.2 %
GAAP Net Income (Loss) Per Share - Basic $ (0.29 ) $ 0.22   (231.1 )%
Non-GAAP Net Income Per Share – Basic** $ 0.52   $ 0.28   85.7 %
GAAP Net Income (Loss) Per Share – Diluted $ (0.29 ) $ 0.20   (242.1 )%
Non-GAAP Net Income Per Share – Diluted** $ 0.49   $ 0.26   88.5 %
As of September 30, 2023, and December 31, 2022
Cash and Cash Equivalents
$ 120,971   $ 298,395   (59.4 %)

**Statements made in this press release include non-GAAP financial measures. Such information is provided as additional information and not as an alternative to Catalyst's financial statements presented in accordance with U.S. generally accepted accounting principles (GAAP). These non-GAAP financial measures are intended to enhance an overall understanding of Catalyst's current financial performance. Catalyst believes that the non-GAAP financial measures presented in this press release provide investors and prospective investors with an alternative method for assessing Catalyst's operating results in a manner that Catalyst believes is focused on the performance of ongoing operations and provides a more consistent basis for comparison between periods. Non-GAAP financial measures should not be considered in isolation or as a substitute for comparable GAAP accounting. Further, non-GAAP measures of net income used by Catalyst may be different from and not directly comparable to similarly titled measures used by other companies.

The non-GAAP financial measure included in this press release excludes from the calculation of net income (i) the expense associated with non-cash stock-based compensation, (ii) non-cash depreciation expense, (iii) non-cash amortization of intangible assets expense, (iv) the provision (benefit) for income taxes and (v) acquired in-process research & development costs. Non-GAAP income per share is calculated by dividing non-GAAP income by the weighted average shares outstanding. See the "Reconciliation of Non-GAAP Metrics" table below.

Recent Business Highlights

  • Achieved record total net revenues of $102.7 million, reflecting a YoY increase of 79.4%
  • Reached new all-time high FIRDAPSE® net product revenue of $66.2 million, reflecting an exceptional 15.8% year-over-year growth increase and 23.1% growth increase YTD.
  • Achieved FYCOMPA® net product revenue of $36.4 million, establishing a 5.2% full-quarter increase compared to Q2 2023.
  • Raised 2023 full-year total revenue guidance to between $390 million and $395 million.
  • Announced FDA approval of AGAMREE® (vamorolone), a novel corticosteroid for the treatment of Duchenne muscular dystrophy.
  • Anticipate AGAMREE commercial launch by our neuromuscular franchise teams in the first quarter of 2024.
  • sNDA seeking to increase FIRDAPSE (amifampridine) maximum daily dose to 100mg for the treatment of Lambert-Eaton myasthenic syndrome was accepted for filing with a PDUFA action date of June 4, 2024.
  • Two new patents for FIRDAPSE have recently been allowed and upon issuance will be added to the FDA's Orange Book further strengthening our intellectual property portfolio for FIRDAPSE.
  • Expect submission of NDA for FIRDAPSE (amifampridine) by DyDo Pharma to PMDA in Japan by the end of 2023. Plans are being developed to expand the global footprint for FIRDAPSE into other Asian and South American markets through strategic partnerships upon acceptance of the NDA in Japan.
  • Active due diligence is underway on several epilepsy and other neuroscience related opportunities, which hold further strategic potential for 2024 if a transaction is successfully completed.
  • Appointed Richard J. Daly as the Company's new CEO, effective on January 1, 2024.
  • Announced that Patrick J. McEnany, who will retire as the Company's CEO at the end of the year, was honored with the 2023 Lifetime Achievement Award by BioFlorida.

Financial Results for the Third Quarter 2023

Product Revenues, Net: Product revenues, net in the third quarter of 2023, were $102.6 million, compared to $57.2 million for the third quarter of 2022, representing an increase of 79.5% year-over-year.

Research and Development Expenses: Research and development expenses were $83.7 million in the third quarter of 2023 compared to $8.3 million for the third quarter of 2022. The increase in R&D for the third quarter 2023 is driven by a one-time charge of $81.5 million for in-process research and development (IPR&D) in connection with the asset acquisition of AGAMREE (vamorolone) during July 2023.

Selling, General, and Administrative Expenses: Selling, general, and administrative expenses for the third quarter of 2023 were $33.6 million, compared to $13.6 million in the third quarter of 2022.

Amortization of Intangible Assets: Amortization of intangible assets was $8.5 million in the third quarter of 2023, compared to $518 thousand in the third quarter of 2022. Intangible assets acquired after the third quarter of 2022 relate to the FYCOMPA rights acquired in the first quarter of 2023.

GAAP Net Income (Loss): GAAP net loss for the third quarter of 2023 was ($30.8) million (($0.29) per basic and diluted share), compared to net income of $22.7 million ($0.22 per basic share and $0.20 per diluted share) for the third quarter of 2022, representing a 235.2% decrease YoY.

Non-GAAP Net Income: Non-GAAP net income for the third quarter of 2023 was $55.9 million ($0.52 per basic share and $0.49 per diluted share), compared to $28.6 million ($0.28 per basic share and $0.26 per diluted share) for the third quarter of 2022, representing an 87.5% increase YoY for each basic share and an 88.5% increase YoY for each diluted share.

Cash and Cash Equivalents: Cash and cash equivalents were $121.0 million as of September 30, 2023.

2023 Financial Guidance: The Company forecasts full-year 2023 total revenues, including FYCOMPA, to be between $390 million and $395 million, representing an 82% to 84% increase in total revenues compared to 2022. Key guidance assumptions in this forecast reflect a continued recovery in macroeconomic and healthcare activity throughout 2023 related to the current COVID-19 environment.

More detailed financial information and analysis regarding the Company's financial position on September 30, 2023, and its results of operations for the three and nine-month periods ended on that date, can be found in the Company's Quarterly Report on Form 10-Q filed with the U.S. Securities and Exchange Commission ("SEC") on November 8, 2023.

Conference Call & Webcast Details
The Company will host a conference call and webcast on Thursday, November 9, 2023, at 8:30 AM ET to discuss the financial results and provide a business update.

U.S./Canada Dial-in Number:   (877) 407-8912
International Dial-in Number:   (201) 689-8059

A webcast will be accessible under the investor section on the Company's website at A webcast replay will be available on the Catalyst website for 30 days after the event.

About Catalyst Pharmaceuticals

With exceptional patient focus, Catalyst is committed to developing and commercializing innovative first-in-class medicines that address rare neurological and epileptic diseases. Catalyst's flagship U.S. commercial product is FIRDAPSE® (amifampridine) Tablets 10 mg, approved for the treatment of Lambert-Eaton myasthenic syndrome ("LEMS") for adults and for children ages six to seventeen. In January 2023, Catalyst acquired the U.S. commercial rights to FYCOMPA® (perampanel) CIII, a prescription medicine approved in people with epilepsy aged four and older alone or with other medicines to treat partial-onset seizures with or without secondarily generalized seizures and with other medicines to treat primary generalized tonic-clonic seizures for people with epilepsy aged 12 and older. Further, Canada's national healthcare regulatory agency, Health Canada, has approved the use of FIRDAPSE for the treatment of adult patients in Canada with LEMS. Finally, on July 18, 2023, Catalyst acquired an exclusive license for North America for AGAMREE® (vamorolone) oral suspension 40 mg/mL, a novel corticosteroid treatment for Duchenne Muscular Dystrophy. AGAMREE previously received FDA Orphan Drug and Fast Track designations and was approved by the FDA for commercialization in the U.S. on October 26, 2023.

For more information about Catalyst Pharmaceuticals, Inc., visit the Company's website at For Full Prescribing and Safety Information for FIRDAPSE®, visit For Full Prescribing Information, including Boxed WARNING for FYCOMPA®, please visit For Full Prescribing Information for AGAMREE, please visit

Forward-Looking Statements

This press release contains forward-looking statements. Forward-looking statements involve known and unknown risks and uncertainties, which may cause Catalyst's actual results in future periods to differ materially from forecasted results. A number of factors, including (i) whether AGAMREE can be successfully launched and whether that launch will occur in the first quarter of 2024, (ii) whether AGAMREE's commercialization will be successful and accretive to Catalyst (iii) Catalyst's ability to continue to sell its current products, (iv) whether Catalyst will continue to be profitable and cash flow positive, (v) whether Catalyst's total revenue forecast for 2023 will prove to be accurate, (vi) whether Catalyst will complete an acquisition of an epilepsy or other neuroscience related opportunity, and the timing of such acquisition; and (vii) those factors described in Catalyst's Annual Report on Form 10-K for the 2022 fiscal year, Catalyst's Quarterly Report on Form 10-Q for the second quarter of 2023, and Catalyst's other filings with the SEC, could adversely affect Catalyst. Copies of Catalyst's filings with the SEC are available from the SEC, may be found on Catalyst's website, or may be obtained upon request from Catalyst. Catalyst does not undertake any obligation to update the information contained herein, which speaks only as of this date.

Source: Catalyst Pharmaceuticals, Inc.



(in thousands, except share data)
  For the Three Months
Ended September 30,
  For the Nine Months
Ended September 30,
    2023       2022       2023       2022
Product revenue, net $ 102,617     $ 57,173     $ 287,398     $ 153,255
License and other revenue   71       71       238       191
Total revenues   102,688       57,244       287,636       153,446
Operating costs and expenses:              
Cost of sales (a)   14,167       9,665       36,158       23,198
Research and development   83,662       8,310       91,178       15,696
Selling, general and administrative (a)   33,560       13,649       91,674       42,997
Amortization of intangible assets   8,487       518       23,506       518
Total operating costs and expenses   139,876       32,142       242,516       82,409
Operating income (loss)   (37,188 )     25,102       45,120       71,037
Other income (expense), net   (833 )     905       2,684       674
Net income (loss) before income taxes   (38,021 )     26,007       47,804       71,711
Income tax provision (benefit)   (7,257 )     3,259       11,238       14,103
Net income (loss) $ (30,764 )   $ 22,748     $ 36,566     $ 57,608
Net income (loss) per share:              
Basic $ (0.29 )   $ 0.22     $ 0.34     $ 0.56
Diluted $ (0.29 )   $ 0.20     $ 0.32     $ 0.52
Weighted average shares outstanding:              
Basic   106,568,137       103,318,572       106,133,077       102,967,280
Diluted   106,568,137       111,986,025       113,751,370       110,352,214
(a) exclusive of amortization of intangible assets


(in thousands, except share data)
    For the Three Months
Ended September 30,
    For the Nine Months
Ended September 30,
    2023       2022       2023       2022
GAAP net income (loss): $ (30,764 )   $ 22,748     $ 36,566     $ 57,608
Non-GAAP adjustments:              
Stock-based compensation expense   3,810       2,055       10,000       5,981
Depreciation   81       35       232       106
Amortization of intangible assets   8,487       518       23,506       518
Income tax provision (benefit)   (7,257 )     3,259       11,238       14,103
In-process R&D   81,513       --       81,513       --
Non-GAAP net income (loss) $ 55,870     $ 28,615     $ 163,055     $ 78,316
Non-GAAP net income per share:                            
Basic $ 0.52     $ 0.28     $ 1.54     $ 0.76
Diluted $ 0.49     $ 0.26     $ 1.43     $ 0.71
Weighted average shares outstanding:                            
Basic   106,568,137       103,318,572       106,133,077       102,967,280
Diluted   113,551,919       111,986,025       113,751,370       110,352,214
(in thousands)
  September 30,
  December 31,
Current Assets:      
Cash and cash equivalents $ 120,971   $ 298,395
Accounts receivable, net   48,049     10,439
Inventory   9,035     6,805
Prepaid expenses and other current assets   13,962     5,167
Total current assets   192,017     320,806
Operating lease right-of-use asset   2,575     2,770
Property and equipment, net   1,186     847
License and acquired intangibles, net   167,108     32,471
Deferred tax assets, net   37,428     18,736
Investment in equity securities   12,897     --
Total assets $ 413,211   $ 375,630
Liabilities and Stockholders' Equity      
Current Liabilities:      
Accounts payable $ 4,598   $ 3,975
Accrued expenses and other liabilities   53,208     53,613
Total current liabilities   57,806     57,588
Operating lease liability, net of current portion   3,282     3,557
Other non-current liabilities   3,575     14,064
Total liabilities   64,663     75,209
Total stockholders' equity   348,548     300,421
Total liabilities and stockholders' equity $ 413,211   $ 375,630

Contact information: Investor Contact Mary Coleman Catalyst Pharmaceuticals, Inc. (305) 420-3200 Media Contact David Schull Russo Partners (858) 717-2310

Primary Logo

Back to news