MannKind Corporation Reports First Quarter 2025 Financial Results and Provides Business Update

Conference call to provide corporate updates today at 9:00 am ET

  • 1Q 2025 revenues of $78M, +18% v. 1Q 2024
  • 1Q 2025 net income of $13M, + 24% v. 1Q 2024
  • 1Q 2025 non-GAAP net income of $22M, +43% v. 1Q 2024
  • Advanced pipeline:
    • Expect to submit sBLA for Afrezzaยฎ in pediatric patients in mid-2025
    • MNKD-101: NTM global Phase 3 trial enrollment on track for interim analysis
    • MNKD-201: Expect to continue to next phase of global development in 2H 2025

DANBURY, Conn. and WESTLAKE VILLAGE, Calif., May 08, 2025 (GLOBE NEWSWIRE) -- MannKind Corporation (Nasdaq: MNKD) today reported financial results for the first quarter 2025 and provided a business update.

โ€œThe first quarter was marked by strong year-over-year NRx growth in Afrezza, substantial Tyvaso DPI-related revenues and continued progress in our Phase 3 trial of MNKD-101 (clofazimine inhalation suspension) in NTM lung disease,โ€ said Michael Castagna, PharmD, Chief Executive Officer of MannKind Corporation. โ€œWe expect to file for approval of Afrezza in the pediatric population this summer and to continue developing our MNKD-201 (nintedanib DPI) program in IPF.โ€

1Q 2025 Business Update and Upcoming Milestones

Afrezza INHALE-1 Pediatric Phase 3 clinical trial

  • Met with the FDA to obtain guidance on a supplemental Biologics License Application (sBLA) for the pediatric population expected to be filed in mid-2025
  • Topline results from the full study pediatric data set with the safety extension expected in 2Q 2025

Clofazimine Inhalation Suspension (MNKD-101) Phase 3 global clinical trial (ICON-1)

  • 85% of anticipated sites have been activated in five countries (U.S., Japan, Australia, South Korea, Taiwan)
  • 55 patients randomized in four countries (U.S., Japan, Australia, South Korea)
  • Expect to meet the interim enrollment target of 100 patients by YE 2025

Nintedanib DPI (MNKD-201)

  • Planning to advance into the next phase of global development in 2H 2025

Endocrine Business Unit

  • Afrezza INHALE-3 Phase 4 30-week data published in two articles in Diabetes Technology & Therapeutics
  • Label application to update initial Afrezza conversion dose submitted to FDA; currently under review
  • Afrezza performance 1Q 2025 compared to 1Q 2024: 20% NRx growth; 14% TRx growth

Corporate and Financial

  • Cash, cash equivalents and investments as of Marchย 31, 2025 totaled $198 million
  • Majority of revenue and future pipeline programs are derived from MannKind's U.S.-based manufacturing facility in Danbury, CT, mitigating potential tariff exposure

First Quarter 2025 Financial Results

Revenues

ย ย Three Months
Ended Marchย 31,
ย 
ย ย 2025ย ย 2024ย ย $ Changeย ย % Changeย 
Revenuesย (Dollars in thousands)ย 
Royaltiesย $30,005ย ย $22,651ย ย $7,354ย ย ย 32%
Collaborations and servicesย ย 29,376ย ย ย 24,848ย ย $4,528ย ย ย 18%
Afrezzaย ย 14,887ย ย ย 14,438ย ย $449ย ย ย 3%
V-Goย ย 4,086ย ย ย 4,326ย ย $(240)ย ย (6%)
Total revenuesย $78,354ย ย $66,263ย ย $12,091ย ย ย 18%
ย 

Total revenues increased $12.0 million, or 18%, in the first quarter of 2025 compared to the same period in the prior year. Revenue increases were driven by higher royalties primarily due to increased patient demand for Tyvaso DPIยฎ and higher revenue from collaborations and services due to increased product sold to United Therapeutics Corporation. Commercial product revenue remained consistent with the prior year period due to an increase in net revenue for Afrezza, mainly due to higher demand and price, partially offset by a decrease in net revenue for V-Goยฎ due to lower demand.

Operating Expenses and Other Financial Highlights

  • Research and development expenses were $11.0 million for the first quarter of 2025 compared to $10.0 million for the same period in 2024, an increase of 10%. The increase was primarily attributable to increased expenditures for development activities, including a Phase 3 clinical study for MNKD-101, clinical production scale up for MNKD-201, and personnel costs primarily due to additional headcount as a result of MannKind's transaction with Pulmatrix, Inc. in the third quarter of 2024, which bolstered our research capabilities and capacity.
  • Selling, general and administrative expenses were $25.0 million for the first quarter of 2025 compared to $22.3 million for the same period in 2024, an increase of 12%. This increase was primarily attributable to increases in headcount, personnel costs and Afrezza promotional costs, partially offset by a loss of $1.2 million in the prior year period for estimated returns associated with sales of V-Go that pre-dated MannKind's acquisition of the product.
  • For the first quarter of 2025, MannKind reported net income of $13.2 million, or $0.04 earnings per share โ€“ basic, compared to net income of $10.6 million, or $0.04 earnings per share โ€“ basic, for the same period in 2024, an increase in net income of $2.5 million, or 24%.
  • For the first quarter of 2025, MannKind reported non-GAAP net income of $21.6 million, or $0.07 earnings per share โ€“ basic, compared to non-GAAP net income of $15.1 million, or $0.06 earnings per shareย  โ€“ basic, for the same period in 2024, an increase in net income of $6.5 million, or 43%. For a reconciliation of GAAP reported net income and net income per share for basic weighted average shares to these non-GAAP measures, please see Non-GAAP Measures below.

Conference Call

MannKind will host a conference call and presentation webcast to discuss these results today at 9:00 a.m. Eastern Time. The webcast will be accessible via a link on MannKindโ€™s website. A replay will also be available in the same location within 24 hours after the call and accessible for approximately 90 days.

About MannKind

MannKind Corporation (Nasdaq: MNKD) focuses on the development and commercialization of innovative inhaled therapeutic products and devices to address serious unmet medical needs for those living with endocrine and orphan lung diseases.

We are committed to using our formulation capabilities and device engineering prowess to lessen the burden of diseases such as diabetes, nontuberculous mycobacterial (NTM) lung disease, pulmonary fibrosis, and pulmonary hypertension.ย Our signature technologies โ€“ dry-powder formulations and inhalation devices โ€“ offer rapid and convenient delivery of medicines to the deep lung where they can exert an effect locally or enter the systemic circulation, depending on the target indication.

With a passionate team of Mannitarians collaborating nationwide, we are on a mission to give people control of their health and the freedom to live life.

Please visit mannkindcorp.com to learn more, and follow us on LinkedIn, Facebook, X or Instagram.

Forward-Looking Statements

Statements in this press release that are not statements of historical fact are forward-looking statements that involve risks and uncertainties. These statements include, without limitation, statements regarding MannKind's expectations about the development of Afrezza for the pediatric population, MNKD-101 and MNKD-201, including the expected timing for regulatory filings and patient enrollment timelines. Words such as โ€œbelieves,โ€ โ€œanticipates,โ€ โ€œplans,โ€ โ€œexpects,โ€ โ€œintend,โ€ โ€œwill,โ€ โ€œgoal,โ€ โ€œpotentialโ€ and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon MannKindโ€™s current expectations. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks associated with developing product candidates; risks and uncertainties related to unforeseen delays that may impact the timing of clinical trials and reporting data; risks associated with the regulatory review process; and other risks detailed in MannKindโ€™s filings with the Securities and Exchange Commission (โ€œSECโ€), including under the โ€œRisk Factorsโ€ heading of its Annual Report on Form 10-K for the year ended Decemberย 31, 2024, filed with the SEC on February 26, 2025, as updated by the "Risk Factors" in its Quarterly Report on Form 10-Q for the quarterly period ended Marchย 31, 2025, being filed with the SEC later today. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. All forward-looking statements are qualified in their entirety by this cautionary statement, and MannKind undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date of this press release.

Tyvaso DPI is a trademark of United Therapeutics Corporation.

AFREZZA, MANNKIND, and V-GO are registered trademarks of MannKind Corporation.


MANNKIND CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS
ย 
ย ย Three Months
Ended Marchย 31,
ย 
ย ย 2025ย ย 2024ย 
ย ย (In thousands except per share data)ย 
Revenues:ย ย ย ย ย ย 
Commercial product salesย $18,973ย ย $18,764ย 
Collaborations and servicesย ย 29,376ย ย ย 24,848ย 
Royaltiesย ย 30,005ย ย ย 22,651ย 
Total revenuesย ย 78,354ย ย ย 66,263ย 
Expenses:ย ย ย ย ย ย 
Cost of goods sold โ€“ commercialย ย 3,768ย ย ย 3,819ย 
Cost of revenue โ€“ collaborations and servicesย ย 13,748ย ย ย 14,779ย 
Research and developmentย ย 11,022ย ย ย 10,013ย 
Selling, general and administrativeย ย 25,014ย ย ย 22,329ย 
Loss (gain) on foreign currency transactionย ย 2,509ย ย ย (1,399)
Total expensesย ย 56,061ย ย ย 49,541ย 
Income from operationsย ย 22,293ย ย ย 16,722ย 
Other income (expense):ย ย ย ย ย ย 
Interest income, netย ย 1,956ย ย ย 3,434ย 
Interest expense on liability for sale of future royaltiesย ย (3,577)ย ย (4,248)
Interest expense on financing liabilityย ย (2,410)ย ย (2,447)
Interest expenseย ย (4,645)ย ย (2,567)
Total other expenseย ย (8,676)ย ย (5,828)
Income before income tax expenseย ย 13,617ย ย ย 10,894ย 
Income tax expenseย ย 459ย ย ย 264ย 
Net incomeย $13,158ย ย $10,630ย 
Net income per share โ€“ basicย $0.04ย ย $0.04ย 
Weighted average shares used to compute net income per share โ€“ basicย ย 303,481ย ย ย 270,356ย 
Net income per share โ€“ dilutedย $0.04ย ย $0.04ย 
Weighted average shares used to compute net income per share โ€“ dilutedย ย 320,897ย ย ย 324,733ย 
ย 


MANNKIND CORPORATION AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
ย 
ย ย Marchย 31, 2025ย ย Decemberย 31, 2024ย 
ย ย (In thousands except share
and per share data)
ย 
ASSETSย ย ย ย ย ย 
Current assets:ย ย ย ย ย ย 
Cash and cash equivalentsย $47,312ย ย $46,339ย 
Short-term investmentsย ย 134,229ย ย ย 150,917ย 
Accounts receivable, netย ย 28,900ย ย ย 11,804ย 
Inventoryย ย 28,892ย ย ย 27,886ย 
Prepaid expenses and other current assetsย ย 34,404ย ย ย 31,360ย 
Total current assetsย ย 273,737ย ย ย 268,306ย 
Restricted cashย ย 739ย ย ย 737ย 
Long-term investmentsย ย 16,681ย ย ย 5,482ย 
Property and equipment, netย ย 83,781ย ย ย 85,365ย 
Goodwillย ย 1,931ย ย ย 1,931ย 
Other intangible assetsย ย 5,217ย ย ย 5,265ย 
Other assetsย ย 28,055ย ย ย 26,757ย 
Total assetsย $410,141ย ย $393,843ย 
ย ย ย ย ย ย ย 
LIABILITIES AND STOCKHOLDERS' DEFICITย ย ย ย ย ย 
Current liabilities:ย ย ย ย ย ย 
Accounts payableย $5,041ย ย $6,792ย 
Accrued expenses and other current liabilitiesย ย 40,103ย ย ย 40,293ย 
Senior convertible notes โ€“ currentย ย 36,109ย ย ย โ€”ย 
Liability for sale of future royalties โ€“ currentย ย 12,802ย ย ย 12,283ย 
Financing liability โ€“ currentย ย 10,125ย ย ย 10,062ย 
Deferred revenue โ€“ currentย ย 11,757ย ย ย 12,407ย 
Total current liabilitiesย ย 115,937ย ย ย 81,837ย 
Liability for sale of future royalties โ€“ long termย ย 137,420ย ย ย 137,362ย 
Financing liability โ€“ long termย ย 93,665ย ย ย 93,877ย 
Deferred revenue โ€“ long termย ย 47,360ย ย ย 51,160ย 
Recognized loss on purchase commitments โ€“ long termย ย 60,713ย ย ย 58,204ย 
Operating lease liabilityย ย 11,141ย ย ย 11,645ย 
Milestone liabilitiesย ย 2,523ย ย ย 2,523ย 
Senior convertible notesย ย โ€”ย ย ย 36,051ย 
Total liabilitiesย ย 468,759ย ย ย 472,659ย 
Stockholders' deficit:ย ย ย ย ย ย 
Undesignated preferred stock, $0.01 par value โ€“ 10,000,000 shares authorized; no shares issued or outstanding as of March 31, 2025 or December 31, 2024ย ย โ€”ย ย ย โ€”ย 
Common stock, $0.01 par value โ€“ 800,000,000 shares authorized; 303,918,969 and 302,959,782 shares issued and outstanding as of March 31, 2025 and December 31, 2024, respectivelyย ย 3,039ย ย ย 3,029ย 
Additional paid-in capitalย ย 3,125,830ย ย ย 3,118,865ย 
Accumulated other comprehensive incomeย ย 1,174ย ย ย 1,109ย 
Accumulated deficitย ย (3,188,661)ย ย (3,201,819)
Total stockholders' deficitย ย (58,618)ย ย (78,816)
Total liabilities and stockholders' deficitย $410,141ย ย $393,843ย 
ย 

Non-GAAP Measures

To supplement MannKind's condensed consolidated financial statements presented under GAAP, we are presenting non-GAAP financial measures for net income and net income per share โ€“ basic. We are providing these non-GAAP financial measures, which are among the indicators management uses as a basis for evaluating our financial performance, to disclose additional information to facilitate the comparison of past and present operations. We believe that these non-GAAP financial measures, when considered together with our GAAP financial results, provide management and investors with an additional understanding of our business operating results, including underlying trends.

These non-GAAP financial measures are not meant to be considered in isolation or as a substitute for comparable GAAP measures; should be read in conjunction with our condensed consolidated financial statements prepared in accordance with GAAP; have no standardized meaning prescribed by GAAP; and are not prepared under any comprehensive set of accounting rules or principles. In addition, from time to time in the future, there may be other items that we may exclude for purposes of our non-GAAP financial measures; and we may cease to exclude items that we have historically excluded for purposes of our non-GAAP financial measures. Likewise, we may determine to modify the nature of its adjustments to arrive at our non-GAAP financial measures. Because of the non-standardized definitions of non-GAAP financial measures, the non-GAAP financial measures as used by us in this Quarterly Report on Form 10-Q have limits in their usefulness to investors and may be calculated differently from, and therefore may not be directly comparable to, similarly titled measures used by other companies.

The following table reconciles our financial measures for net income and net income per share ("EPS") for basic weighted average shares as reported in our condensed consolidated statements of operations to a non-GAAP presentation:

ย Three Months Ended
March 31,
ย 
ย 2025ย ย 2024ย 
ย Net Incomeย ย Basic EPSย ย Net Incomeย ย Basic EPSย 
ย (In thousands except per share data)ย 
GAAP reported net income$13,158ย ย $0.04ย ย $10,630ย ย $0.04ย 
Non-GAAP adjustments:ย ย ย ย ย ย ย ย ย ย ย 
Sold portion of royalty revenue (1)ย (3,000)ย ย (0.01)ย ย (2,265)ย ย (0.01)
Interest expense on liability for sale of future royaltiesย 3,577ย ย ย 0.01ย ย ย 4,248ย ย ย 0.03ย 
Stock compensationย 5,385ย ย ย 0.02ย ย ย 3,885ย ย ย 0.01ย 
Loss (gain) on foreign currency transactionย 2,509ย ย ย 0.01ย ย ย (1,399)ย ย (0.01)
Non-GAAP adjusted net income$21,629ย ย $0.07ย ย $15,099ย ย $0.06ย 
Weighted average shares used to compute net income per share โ€“ basicย 303,481ย ย ย ย ย ย 270,356ย ย ย ย 

_________________

(1)Represents the non-cash portion of the 1% royalty on net sales of Tyvaso DPI which is remitted to the royalty purchaser and recognized as royalties from collaborations in our consolidated statements of operations.

MannKind Contacts:
Investor Relations
Ana Kapor
(818) 661-5000
Email: ir@mnkd.com

Media Relations
Christie Iacangelo
(818) 292-3500
Email: media@mnkd.com

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