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MannKind Corporation (Nasdaq: MNKD) Q2 2026 revenue rises 43% as costs drive loss

(High)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

MannKind Corporation reported Q2 2026 total revenues of $109,374 (thousands), a 43% increase from Q2 2025, driven by the addition of Furoscix, higher collaborations and services revenue, and royalties tied to Tyvaso DPI. Commercial product sales were $41,982 (thousands), including Furoscix net sales of $22,191 (thousands) and Afrezza net sales of $17,021 (thousands). For the first six months of 2026, total revenues reached $199,544 (thousands), up 29% year over year.

Higher cost of goods, research and development, and selling, general and administrative expenses, largely associated with Furoscix and pipeline advancement, led to a Q2 2026 net loss of $19,032 (thousands), or $0.06 per basic share, compared with net income of $668 (thousands) a year earlier. Non-GAAP adjusted net loss was $2,660 (thousands) versus non-GAAP income of $13,901 (thousands). Cash, cash equivalents and investments totaled $111 million as of June 30, 2026, and a $50 million private placement closed on July 24, 2026 to fund a $45 million contingent value right payment following FDA approval of the Furoscix ReadyFlow autoinjector. During 2026, MannKind also received FDA approval for a pediatric indication for Afrezza and reported positive Phase 1b data for its nintedanib DPI program while preparing an IND for ralinepag DPI.

Positive

  • Total revenues rose 43% year over year in Q2 2026 to $109,374 (thousands), with commercial product sales and collaborations/royalties expanding, helped by the addition of Furoscix and increased Tyvaso DPI-related royalties.
  • Six-month 2026 revenues grew 29% to $199,544 (thousands), reflecting broader contributions from Furoscix, higher collaborations and services revenue, and growing royalty streams.

Negative

  • Profitability deteriorated, with a Q2 2026 net loss of $19,032 (thousands) versus prior-year income, as selling, general and administrative expenses nearly doubled to $58,302 (thousands).
  • Non-GAAP results also weakened, showing an adjusted net loss of $2,660 (thousands) for Q2 2026 compared with non-GAAP income of $13,901 (thousands) in Q2 2025.

Insights

Analyzing...

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Q2 2026 Total Revenues $109,374 (thousands) Three months ended June 30, 2026; 43% increase vs $76,527 (thousands) in Q2 2025
Six-month 2026 Total Revenues $199,544 (thousands) Six months ended June 30, 2026; 29% increase vs $154,881 (thousands) in 2025
Q2 2026 Net (Loss) Income $(19,032) (thousands) Net loss for three months ended June 30, 2026 vs $668 (thousands) income in Q2 2025
Q2 2026 Non-GAAP Adjusted Net (Loss) Income $(2,660) (thousands) Non-GAAP adjusted net loss for Q2 2026 vs $13,901 (thousands) non-GAAP income in Q2 2025
Q2 2026 Selling, General and Administrative Expense $58,302 (thousands) Three months ended June 30, 2026; up from $31,622 (thousands) in Q2 2025
Cash, Cash Equivalents and Investments $111 million Corporate update for balances as of June 30, 2026
Senior Convertible Notes – Current $0 Current portion reduced from $36,280 (thousands) at December 31, 2025 to zero at June 30, 2026
Term Loan Balance $319,085 (thousands) Term loan outstanding as of June 30, 2026
Furoscix ReadyFlow Autoinjector medical
"support the launches associated with the recent approvals of the pediatric indication for Afrezza and the Furoscix ReadyFlow Autoinjector"
contingent consideration financial
"Change in fair value of contingent consideration"
Contingent consideration is an additional payment agreed when one company buys another that will be paid later only if specific future targets are met, such as revenue, profit, or regulatory milestones. It matters to investors because it shifts risk between buyer and seller and affects the acquiring company's future cash flow and reported value — like promising a bonus after results are proven.
liability for sale of future royalties financial
"Interest expense on liability for sale of future royalties"
IPR&D - ReadyFlow Formulation financial
"IPR&D - ReadyFlow Formulation"
non-GAAP adjusted net (loss) income financial
"Non-GAAP adjusted net (loss) income"
Breakthrough T1D grant medical
"Awarded Breakthrough T1D grant supporting advancement of INHALE-1ST"
Q2 2026 Total Revenues $109,374 (thousands) up 43% from $76,527 (thousands) in Q2 2025
Six-month 2026 Total Revenues $199,544 (thousands) up 29% from $154,881 (thousands) in 2025
Q2 2026 Net (Loss) Income $(19,032) (thousands) vs net income of $668 (thousands) in Q2 2025
Q2 2026 Non-GAAP Adjusted Net (Loss) Income $(2,660) (thousands) vs non-GAAP income of $13,901 (thousands) in Q2 2025

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FAQ

What were MannKind (MNKD) Q2 2026 revenues and how did they change year over year?

MannKind (MNKD) generated Q2 2026 total revenues of $109,374 (thousands), a 43% increase from $76,527 (thousands) in Q2 2025. Growth was driven by adding Furoscix to the product portfolio and higher collaborations, services, and royalty revenues, including from Tyvaso DPI.

Did MannKind (MNKD) report a profit or loss for Q2 2026, and what was EPS?

MannKind (MNKD) reported a Q2 2026 net loss of $19,032 (thousands), or basic EPS of $(0.06), compared with net income of $668 (thousands) and basic EPS of $0.00 in Q2 2025, reflecting higher operating expenses and interest costs.

How did Furoscix and Afrezza perform for MannKind (MNKD) in Q2 2026?

In Q2 2026, Furoscix net sales were $22,191 (thousands), while Afrezza net sales were $17,021 (thousands). Furoscix contributed new revenue after the scPharma acquisition, whereas Afrezza revenue declined versus Q2 2025 as shown in the detailed revenue table.

What key FDA approvals and clinical milestones did MannKind (MNKD) achieve in 2026?

MannKind (MNKD) received FDA approval for Afrezza in children 6 and older and FDA approval of the Furoscix ReadyFlow autoinjector. It also reported positive Phase 1b INFLO-1 data for nintedanib DPI and began site activation and enrollment for the global Phase 2 INFLO-2 study.

What is MannKind (MNKD)'s cash position and recent financing activity?

As of June 30, 2026, MannKind (MNKD) held $111 million in cash, cash equivalents and investments. On July 24, 2026 it closed a $50 million private placement, with proceeds intended to fund a $45 million contingent value right payment tied to Furoscix ReadyFlow approval.

How do MannKind (MNKD)'s non-GAAP Q2 2026 results compare with GAAP figures?

For Q2 2026, MannKind (MNKD) reported a GAAP net loss of $19,032 (thousands) and a non-GAAP adjusted net loss of $2,660 (thousands). In Q2 2025, non-GAAP adjusted net income was $13,901 (thousands), highlighting the impact of higher expenses and financing-related items.
0000899460false00008994602026-08-052026-08-05

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 05, 2026

 

 

MannKind Corporation

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

000-50865

13-3607736

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

1 Casper Street

 

Danbury, Connecticut

 

06810

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (818) 661-5000

 

N/A

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.01 per share

 

MNKD

 

The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 


Item 2.02. Results of Operations and Financial Condition.

On August 5, 2026, MannKind Corporation issued a press release, a copy of which is furnished herewith as Exhibit 99.1 and is incorporated herein by reference.

Item 9.01. Financial Statements and Exhibits.

 

Exhibit 99.1

Press release dated August 5, 2026

 

 

Exhibit 104

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 


SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

MannKind Corporation

 

Date: August 5, 2026

By:

/s/ David Thomson, Ph.D., J.D.

David Thomson, Ph.D., J.D.

Corporate Vice President, General Counsel and Secretary

 

 


img208524907_0.gif

MannKind Reports Second Quarter 2026 Financial Results and Provides Business Update

 

Achieved three major catalysts to drive future growth:
o
Launched the pediatric indication of Afrezza® following FDA approval
o
FUROSCIX ReadyFlow™ autoinjector approved for treatment of edema in HF and CKD
o
Positive nintedanib DPI Phase 1b data in IPF patients validates continued Phase 2 advancement
Encouraging early momentum in Afrezza pediatric launch
o
1 in 3 of the top 100 pediatric insulin writers have prescribed
Q2 2026 total revenues of $109.4M, +43% vs. Q2 2025
Conference call and webcast today at 4:30 p.m. ET

 

DANBURY, Conn. and WESTLAKE VILLAGE, Calif., August 5, 2026 (GLOBE NEWSWIRE) -- MannKind Corporation (Nasdaq: MNKD)

a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions for cardiometabolic and orphan lung diseases, today reported financial results for the second quarter of 2026, and provided a business update.

 

“This was a transformative period for MannKind, during which we delivered all three major catalysts we set out to achieve in 2026,” said Michael Castagna, Chief Executive Officer of MannKind. “The two recent FDA approvals are expected to fuel our near-term growth opportunities to help patients living with diabetes, heart failure and CKD. The positive Phase 1b INFLO-1 results for MNKD-201 reduces development risk and strengthens our confidence in the ability of our platform to help people living with IPF and other fibrotic diseases. Together, these milestones validate our diversification strategy and position MannKind for sustainable growth.”

 

Business Update and Upcoming Milestones

Commercial Products

Revenue from marketed products (Afrezza, Furoscix®) grew 27% from Q1 2026 to Q2 2026

Furoscix

Furoscix (furosemide injection) generated $22.2 million in net sales for Q2 2026
Continued growth in Integrated Delivery Networks, increasing doses purchased by 36% over Q1 2026
Record number of nephrology units dispensed, increasing by 67% over Q1 2026
Received FDA approval of Furoscix ReadyFlow™ on July 23, 2026, the first and only autoinjector delivering IV-equivalent diuretic therapy for the treatment of edema in adults with heart failure (HF) or chronic kidney disease (CKD); expected to be commercially available in late August

Afrezza

Afrezza (insulin human) Inhalation Powder generated $17.0 million in net sales for Q2 2026
Received FDA approval of Afrezza on May 29, 2026 for use in children and adolescents ages 6 and older living with diabetes
Awarded Breakthrough T1D grant supporting advancement of INHALE-1ST, a pediatric trial of Afrezza in youth with newly diagnosed type 1 diabetes

 

Development

Nintedanib DPI (MNKD-201)

Topline data readout of U.S. Phase 1b INFLO-1 demonstrates safety and tolerability in IPF patients
Site activation and enrollment underway in the global Phase 2 INFLO-2 study

Ralinepag DPI (MNKD-1501)

On track for IND filing by year end
Received a $5 million payment from United Therapeutics (UT) to support the rapid advancement of ralinepag DPI

 

Corporate Update

Cash, cash equivalents and investments as of June 30, 2026, totaled $111 million
Closed $50 million private placement on July 24, 2026; proceeds will fund the $45 million CVR payment triggered by the FDA approval of Furoscix ReadyFlow

 

 

 

 

 

 

 

 

 


 

 

Second Quarter 2026 Financial Results

 

Revenues

 

 

 

Three Months
Ended June 30,

 

 

 

2026

 

 

2025

 

 

$ Change

 

 

% Change

 

Revenues

 

(Dollars in thousands)

 

Afrezza

 

 

17,021

 

 

 

18,329

 

 

 

(1,308

)

 

 

(7

%)

Furoscix

 

 

22,191

 

 

 

 

 

 

22,191

 

 

N/A

 

V-Go®

 

 

2,770

 

 

 

4,125

 

 

 

(1,355

)

 

 

(33

%)

Collaborations and services

 

 

35,022

 

 

 

22,845

 

 

 

12,177

 

 

 

53

%

Royalties

 

 

32,370

 

 

 

31,228

 

 

 

1,142

 

 

 

4

%

Total revenues

 

$

109,374

 

 

$

76,527

 

 

$

32,847

 

 

 

43

%

 

Total revenues for the second quarter of 2026 increased compared to the same period in the prior year due to the addition of Furoscix to our product portfolio through the October 7, 2025 acquisition of scPharma, as well as increases in collaborations and services revenue, and royalties. The increase in collaborations and services revenue was primarily attributable to increased product sold to UT and revenue earned related to the development of ralinepag DPI. The increase in royalties was due to UT’s increase in net revenue from sales of Tyvaso DPI.

 

Operating Expenses and Other Financial Highlights

 

Cost of goods sold – commercial, excluding amortization of acquired intangible assets, was $14.4 million for the three months ended June 30, 2026, compared to $4.6 million for the same period in 2025.
The increase is primarily attributable to the inclusion of Furoscix into our product portfolio following the acquisition of scPharma in October 2025. Gross margin percentage decreased in the current period due to the inclusion of Furoscix, which has a lower gross margin percentage than Afrezza.

 

Research and development expenses were $18.0 million for the three months ended June 30, 2026, compared to $13.7 million for the same period in 2025, an increase of 32%.
The increase was primarily attributable to the development of the Furoscix ReadyFlow Formulation as well as higher personnel costs following the acquisition of scPharma and increased development costs for MNKD-201, which has begun enrolling subjects. The increase was partially offset by lower clinical development expenses resulting from the discontinuation of the ICoN-1 clinical study for MNKD-101 and the completion of the Afrezza pediatric study (INHALE-1).

 

Selling, general and administrative expenses were $58.3 million for the three months ended June 30, 2026, compared to $31.6 million for the same period in 2025, an increase of 84%.
The increase was primarily related to costs associated with the promotion and support of Furoscix, as well as expanding our field-based teams and activities to support the launches associated with the recent approvals of the pediatric indication for Afrezza and the Furoscix ReadyFlow Autoinjector.

 

Six Months Ended June 30, 2026

 

Revenues

 

 

 

Six Months
Ended June 30,

 

 

 

2026

 

 

2025

 

 

$ Change

 

 

% Change

 

Revenues

 

(Dollars in thousands)

 

Afrezza

 

 

32,294

 

 

 

33,216

 

 

 

(922

)

 

 

(3

%)

Furoscix

 

 

37,684

 

 

 

 

 

 

37,684

 

 

N/A

 

V-Go

 

 

5,911

 

 

 

8,211

 

 

 

(2,300

)

 

 

(28

%)

Collaborations and services

 

 

58,536

 

 

 

52,221

 

 

 

6,315

 

 

 

12

%

Royalties

 

 

65,119

 

 

 

61,233

 

 

 

3,886

 

 

 

6

%

Total revenues

 

$

199,544

 

 

$

154,881

 

 

$

44,663

 

 

 

29

%

 

Total revenues for the six months ended June 30, 2026 increased compared to the same period in the prior year due to the addition of Furoscix to our product portfolio through the October 7, 2025 acquisition of scPharma, as well as increases in collaborations and services revenue, and royalties. The increase in collaborations and services revenue was primarily attributable to an increase in revenue earned related to the development of ralinepag DPI. The increase in royalties was due to UT’s increase in net revenue from sales of Tyvaso DPI.

 

Operating Expenses and Other Financial Highlights

 

Cost of goods sold – commercial, excluding amortization of acquired intangible assets, was $21.9 million for the six months ended

 


 

June 30, 2026, compared to $8.4 million for the same period in 2025.
The increase is primarily attributable to the inclusion of Furoscix into our product portfolio following the acquisition of scPharma in October 2025. Gross margin percentage decreased in the current period due to the inclusion of Furoscix, which has a lower gross margin percentage than Afrezza.

 

Research and development expenses were $35.2 million for the six months ended June 30, 2026, compared to $24.7 million for the same period in 2025, an increase of 43%.
The increase was primarily attributable to the development of the Furoscix ReadyFlow Formulation as well as higher personnel costs following the acquisition of scPharma and increased development costs for MNKD-201, which has begun enrolling subjects. The increase was partially offset by lower clinical development expenses resulting from the discontinuation of the ICoN-1 clinical study for MNKD-101 and the completion of the Afrezza pediatric study (INHALE-1).

 

Selling, general and administrative expenses were $112.4 million for the six months ended June 30, 2026, compared to $56.6 million for the same period in 2025, an increase of 98%.
The increase was primarily related to costs associated with the promotion and support of Furoscix, as well as expanding our field-based teams and activities to support the launches associated with the recent approvals of the pediatric indication for Afrezza and the Furoscix ReadyFlow Autoinjector.

 

Conference Call and Webcast

MannKind will host a conference call and webcast to discuss these results today at 4:30 p.m. Eastern Time. The webcast will be accessible via a link on MannKind’s website at https://investors.mannkindcorp.com/events-and-presentations. 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) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions. Focused on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, and fluid overload in heart failure and chronic kidney disease.

 

With deep expertise in drug-device combinations, MannKind aims to deliver therapies designed to fit seamlessly into daily life.

 

Learn more at mannkindcorp.com.

 

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 the timing for expected commercial availability of Furoscix ReadyFlow and the broadened growth potential for Furoscix; the timing of a planned IND filing of ralinepag DPI; expectations regarding MannKind’s ongoing and planned clinical trials and nonclinical studies; and our being positioned for sustainable growth. Words such as “believes,” “anticipates,” “plans,” “expects,” “intend,” “will,” “goal,” “potential,” “prepare,” “opportunity” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon MannKind’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 safety and other complications of our products and product candidates; risks associated with the regulatory review process; risks associated with competition; manufacturing risks; market adoption risks; and other risks detailed in MannKind’s filings with the Securities and Exchange Commission (“SEC”), including under the “Risk Factors” heading of its Quarterly Report on Form 10-Q for the quarter ended June 30, 2026, 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, FUROSCIX, FUROSCIX READYFLOW, MANNKIND, and V-GO are trademarks of MannKind Corporation.

 

MannKind Contacts:

Investor Relations

Kate Miranda

Email: ir@mnkd.com

 

Media Relations

Christie Iacangelo

Email: media@mnkd.com

 

 


 

 

MANNKIND CORPORATION AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF OPERATIONS

 

 

 

Three Months
Ended June 30,

 

 

Six Months
Ended June 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

 

 

(In thousands except per share data)

 

Revenues:

 

 

 

 

 

 

 

 

 

 

 

 

Commercial product sales

 

$

41,982

 

 

$

22,454

 

 

$

75,889

 

 

$

41,427

 

Collaborations and services

 

 

35,022

 

 

 

22,845

 

 

 

58,536

 

 

 

52,221

 

Royalties

 

 

32,370

 

 

 

31,228

 

 

 

65,119

 

 

 

61,233

 

Total revenues

 

 

109,374

 

 

 

76,527

 

 

 

199,544

 

 

 

154,881

 

Expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Cost of goods sold – commercial, excluding amortization of acquired intangible assets

 

 

14,409

 

 

 

4,607

 

 

 

21,917

 

 

 

8,375

 

Cost of revenue – collaborations and services

 

 

15,131

 

 

 

15,961

 

 

 

25,094

 

 

 

29,709

 

Research and development

 

 

18,001

 

 

 

13,675

 

 

 

35,232

 

 

 

24,697

 

Selling, general and administrative

 

 

58,302

 

 

 

31,622

 

 

 

112,389

 

 

 

56,636

 

Amortization of acquired intangible assets

 

 

4,367

 

 

 

 

 

 

8,734

 

 

 

 

(Gain) loss on foreign currency transaction

 

 

(486

)

 

 

5,363

 

 

 

(1,804

)

 

 

7,872

 

Total expenses

 

 

109,724

 

 

 

71,228

 

 

 

201,562

 

 

 

127,289

 

(Loss) income from operations

 

 

(350

)

 

 

5,299

 

 

 

(2,018

)

 

 

27,592

 

Other income (expense):

 

 

 

 

 

 

 

 

 

 

 

 

Interest income, net

 

 

1,022

 

 

 

1,832

 

 

 

2,452

 

 

 

3,788

 

Interest expense

 

 

(11,894

)

 

 

(285

)

 

 

(19,372

)

 

 

(4,930

)

Interest expense on liability for sale of future royalties

 

 

(510

)

 

 

(3,473

)

 

 

(3,073

)

 

 

(7,050

)

Interest expense on financing liability

 

 

(2,414

)

 

 

(2,433

)

 

 

(4,807

)

 

 

(4,843

)

Loss on settlement of debt

 

 

 

 

 

 

 

 

(917

)

 

 

 

Other expense

 

 

(4,992

)

 

 

 

 

 

(7,769

)

 

 

 

Total other expense

 

 

(18,788

)

 

 

(4,359

)

 

 

(33,486

)

 

 

(13,035

)

(Loss) income before income tax (benefit) expense

 

 

(19,138

)

 

 

940

 

 

 

(35,504

)

 

 

14,557

 

Income tax (benefit) expense

 

 

(106

)

 

 

272

 

 

 

147

 

 

 

731

 

Net (loss) income

 

$

(19,032

)

 

$

668

 

 

$

(35,651

)

 

$

13,826

 

Net (loss) income per share – basic

 

$

(0.06

)

 

$

0.00

 

 

$

(0.12

)

 

$

0.05

 

Weighted average shares used to compute net (loss) income
   per share – basic

 

 

309,191

 

 

 

304,954

 

 

 

308,732

 

 

 

304,222

 

Net (loss) income per share – diluted

 

$

(0.06

)

 

$

0.00

 

 

$

(0.12

)

 

$

0.04

 

Weighted average shares used to compute net (loss) income
   per share – diluted

 

 

309,191

 

 

 

311,484

 

 

 

308,732

 

 

 

312,381

 

 

 

 

 

 

 


 

 

 

MANNKIND CORPORATION AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS

 

 

 

June 30, 2026

 

 

December 31, 2025

 

 

 

(In thousands except share
and per share data)

 

ASSETS

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

52,929

 

 

$

74,882

 

Short-term investments

 

 

58,201

 

 

 

96,464

 

Accounts receivable, net

 

 

43,207

 

 

 

38,367

 

Inventory

 

 

44,419

 

 

 

35,313

 

Prepaid expenses and other current assets

 

 

46,956

 

 

 

46,553

 

Total current assets

 

 

245,712

 

 

 

291,579

 

Restricted cash

 

 

749

 

 

 

745

 

Long-term investments

 

 

 

 

 

5,012

 

Property and equipment, net

 

 

85,160

 

 

 

82,423

 

Goodwill

 

 

67,595

 

 

 

67,595

 

Developed technology - on-body infusor

 

 

181,389

 

 

 

190,027

 

IPR&D - ReadyFlow Formulation

 

 

129,600

 

 

 

129,600

 

Other intangible assets

 

 

4,976

 

 

 

5,072

 

Other assets

 

 

17,123

 

 

 

20,129

 

Total assets

 

$

732,304

 

 

$

792,182

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS' DEFICIT

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

11,042

 

 

$

9,034

 

Accrued expenses and other current liabilities

 

 

60,768

 

 

 

64,628

 

Senior convertible notes – current

 

 

 

 

 

36,280

 

Liability for sale of future royalties – current

 

 

14,292

 

 

 

14,298

 

Contingent consideration – current

 

 

34,015

 

 

 

21,132

 

Financing liability – current

 

 

10,486

 

 

 

10,328

 

Deferred revenue – current

 

 

11,085

 

 

 

15,331

 

Recognized loss on purchase commitments – current

 

 

1,210

 

 

 

 

Total current liabilities

 

 

142,898

 

 

 

171,031

 

Liability for sale of future royalties – long term

 

 

133,552

 

 

 

136,985

 

Financing liability – long term

 

 

92,497

 

 

 

93,092

 

Deferred revenue – long term

 

 

36,857

 

 

 

39,977

 

Recognized loss on purchase commitments – long term

 

 

62,922

 

 

 

65,952

 

Operating lease liability

 

 

9,687

 

 

 

10,689

 

Contingent consideration – long term

 

 

 

 

 

5,114

 

Milestone liabilities

 

 

2,003

 

 

 

2,003

 

Term loan

 

 

319,085

 

 

 

318,361

 

Total liabilities

 

 

799,501

 

 

 

843,204

 

Commitments and contingencies

 

 

 

 

 

 

Stockholders' deficit:

 

 

 

 

 

 

Undesignated preferred stock, $0.01 par value – 10,000,000 shares authorized;
   no shares issued or outstanding as of June 30, 2026 or December 31, 2025

 

 

 

 

 

 

Common stock, $0.01 par value – 800,000,000 shares authorized;
  309,911,682 and 307,832,587 shares issued and outstanding as of
  June 30, 2026 and December 31, 2025, respectively

 

 

3,099

 

 

 

3,078

 

Additional paid-in capital

 

 

3,161,330

 

 

 

3,141,741

 

Accumulated other comprehensive (loss) income

 

 

(19

)

 

 

115

 

Accumulated deficit

 

 

(3,231,607

)

 

 

(3,195,956

)

Total stockholders' deficit

 

 

(67,197

)

 

 

(51,022

)

Total liabilities and stockholders' deficit

 

$

732,304

 

 

$

792,182

 

 

 


 

Non-GAAP Measures

 

To supplement our condensed consolidated financial statements presented under GAAP, we are presenting non-GAAP net (loss) income and non-GAAP net (loss) income per share – basic, which are non-GAAP financial measures. We are providing these non-GAAP financial measures to disclose additional information to facilitate the comparison of past and present operations, and they are among the indicators management uses as a basis for evaluating our financial performance. 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 in the future

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 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 report 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 (loss) income and net (loss) income per share ("EPS") for basic weighted average shares as reported in our condensed consolidated statement of operations to a non-GAAP presentation:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Three Months
Ended June 30,

 

 

Six Months
Ended June 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

 

 

Net Loss

 

 

Basic EPS

 

 

Net Income

 

 

Basic EPS

 

 

Net Loss

 

 

Basic EPS

 

 

Net Income

 

 

Basic EPS

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

GAAP reported net (loss) income

 

$

(19,032

)

 

$

(0.06

)

 

$

668

 

 

$

0.00

 

 

$

(35,651

)

 

$

(0.12

)

 

$

13,826

 

 

$

0.05

 

Non-GAAP adjustments:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Stock compensation

 

 

10,226

 

 

 

0.03

 

 

 

7,520

 

 

 

0.03

 

 

 

16,681

 

 

 

0.05

 

 

 

12,905

 

 

 

0.04

 

Interest expense on liability for sale of future royalties

 

 

510

 

 

 

0.00

 

 

 

3,473

 

 

 

0.01

 

 

 

3,073

 

 

 

0.01

 

 

 

7,050

 

 

 

0.02

 

Sold portion of royalty revenue (1)

 

 

(3,237

)

 

 

(0.01

)

 

 

(3,123

)

 

 

(0.01

)

 

 

(6,512

)

 

 

(0.02

)

 

 

(6,123

)

 

 

(0.02

)

(Gain) loss on foreign currency transaction

 

 

(486

)

 

 

0.00

 

 

 

5,363

 

 

 

0.02

 

 

 

(1,804

)

 

 

(0.01

)

 

 

7,872

 

 

 

0.03

 

Amortization of intangible assets acquired

 

 

4,367

 

 

 

0.01

 

 

 

 

 

 

 

 

 

8,734

 

 

 

0.03

 

 

 

 

 

 

 

Change in fair value of contingent consideration

 

 

4,992

 

 

 

0.02

 

 

 

 

 

 

 

 

 

7,769

 

 

 

0.03

 

 

 

 

 

 

 

Loss on settlement of debt

 

 

 

 

 

 

 

 

 

 

 

 

 

 

917

 

 

 

0.00

 

 

 

 

 

 

 

Non-GAAP adjusted net (loss) income

 

$

(2,660

)

 

$

(0.01

)

 

$

13,901

 

 

$

0.05

 

 

$

(6,793

)

 

$

(0.03

)

 

$

35,530

 

 

$

0.12

 

Weighted average shares used to compute net (loss) income per share – basic

 

 

309,191

 

 

 

 

 

 

304,954

 

 

 

 

 

 

308,732

 

 

 

 

 

 

304,222

 

 

 

 

 

(1)
Represents the non-cash portion of the 1% royalty on net sales of Tyvaso DPI earned during the three and six months ended June 30, 2026 and 2025 which is remitted to the royalty purchaser and recognized as royalties from collaborations in our condensed consolidated statements of operations.

 


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