STOCK TITAN

MannKind swings to $23.2M net loss in Q3 2026

Furoscix ReadyFlow shipments started in mid-September, while Afrezza's pediatric launch coincided with higher new-to-brand prescriptions.

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(High)

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

Form Type
8-K

Rhea-AI Filing Summary

MannKind Corporation reported third-quarter 2026 revenue of $101.9 million, up 24% from $82.1 million a year earlier; commercial product sales were $45.0 million, up 102%. GAAP results were a net loss of $23.2 million, versus $8.0 million net income in Q3 2025. Selling, general and administrative expense rose 111% to $61.4 million, mainly reflecting Furoscix promotion, expanded field teams and launch costs.

Furoscix ReadyFlow was approved and shipments began in mid-September; it represented approximately 75% of Furoscix shipments by late October. Afrezza’s pediatric launch coincided with an approximately 80% increase in average monthly new-to-brand prescriptions in Q3 versus Q2 2026. MannKind reported positive Phase 1b INFLO-1 results for nintedanib DPI, and its global Phase 2 trial is underway.

Cash, cash equivalents and investments totaled $96.6 million as of September 30, 2026. For ralinepag DPI, formulation work was complete, United Therapeutics plans to pursue clinical development, and MannKind anticipates earning $15 million in milestone payments in 2027.

2 points · 0 major

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Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 2 points

How the balance works

Positive

  • Moderate pointThird-quarter revenue rose 24% to $101.9 million year over year.
  • Minor pointCommercial product sales rose 102% to $45.0 million year over year.

Negative

  • Moderate pointThird-quarter net loss: $23.2 million, versus $8.0 million net income.
  • Moderate pointSelling, general and administrative expense rose 111% to $61.4 million.

Filing Explained

MannKind reports it closed a $50 million private placement on July 24, 2026—a sale of securities to selected investors outside a public offering—and says the proceeds funded the $45 million CVR payment triggered by ReadyFlow FDA approval. The release does not give the placement’s share or conversion terms, so its specific ownership effect cannot be sized from this disclosure.

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, or exhibit attachments filed with this report.
Total revenue $101.9 million Third quarter 2026; up 24% from Q3 2025
Commercial product sales $45.0 million Third quarter 2026; up 102% from Q3 2025
GAAP net loss $23.2 million Third quarter 2026; compared with $8.0 million net income in Q3 2025
Selling, general and administrative expense $61.4 million Third quarter 2026; up 111% from Q3 2025
Cash, cash equivalents and investments $96.6 million As of September 30, 2026
Private placement $50 million Closed July 24, 2026
CVR payment $45 million Payment funded by private placement proceeds following FDA approval of Furoscix ReadyFlow
Anticipated ralinepag DPI milestone payments $15 million Anticipated in 2027
Technosphere® DPI platform technical
"validating the Technosphere® DPI platform in IPF"
IPF medical
"clinical validation of Technosphere DPI technology in IPF"
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease where scar tissue builds up in the lungs for reasons doctors don't fully understand, making it harder to breathe over time. For investors, IPF matters because it represents a clear medical need and a regulated market for treatments, so progress in clinical trials, regulatory approvals, or new therapies can materially affect the value of companies working on drugs or devices for this condition—much like a new road that could open access to a previously hard-to-reach town.
CVR payment financial
"proceeds funded the $45 million CVR payment"
non-GAAP adjusted net (loss) income financial
"Non-GAAP adjusted net (loss) income"
available-for-sale investment financial
"Impairment of available-for-sale investment"
Total revenue $101.9 million +24% vs. Q3 2025
Commercial product sales $45.0 million +102% vs. Q3 2025
GAAP net loss $23.2 million Compared with $8.0 million net income in Q3 2025
Selling, general and administrative expense $61.4 million +111% vs. Q3 2025
Guidance

MannKind anticipates earning $15 million in milestone payments in 2027.

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

How much revenue did MNKD report for Q3 2026?

MannKind reported total revenue of $101.9 million for Q3 2026, up 24% from $82.1 million in Q3 2025. Commercial product sales were $45.0 million, up 102% from $22.3 million.

Did MNKD make a profit in Q3 2026?

MannKind reported a GAAP net loss of $23.2 million for Q3 2026, compared with net income of $8.0 million in Q3 2025.

What did MNKD say about its $50 million private placement?

MannKind closed the $50 million private placement on July 24, 2026. The proceeds funded the $45 million CVR payment triggered by FDA approval of Furoscix ReadyFlow.

How many pediatric patients had received Afrezza since launch?

Approximately 2,000 pediatric patients had been treated since launch, and all 60 priority pediatric institutions had prescribed Afrezza.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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false000089946000008994602026-11-052026-11-05

 

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): November 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 November 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 November 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: November 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 Third Quarter 2026 Financial Results and Provides Business Update

 

•
Q3 2026 total revenues of $101.9 million, +24% vs. Q3 2025
•
Q3 2026 commercial product revenue of $45.0 million, +102% vs. Q3 2025
o
Furoscix ReadyFlow™ was approved and shipments commenced mid-September
o
Rapid adoption of Furoscix ReadyFlow, making up approximately 75% of the current weekly Furoscix shipments
o
Afrezza® pediatric launch accounts for an approximately 80% increase in average monthly new-to-brand prescriptions in Q3 vs. Q2 2026
•
Pipeline Advancements
o
Reported positive Phase 1b INFLO-1 results, demonstrating tolerability of nintedanib DPI and clinical validation of Technosphere DPI technology in IPF; global Phase 2 trial underway
•
Conference call and webcast today at 4:30 p.m. ET

 

DANBURY, Conn. and WESTLAKE VILLAGE, Calif., November 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 third quarter of 2026, and provided a business update.

 

“The third quarter marked an important transition for MannKind as we shifted from delivering on three major catalysts to executing against them,” said Michael Castagna, Chief Executive Officer of MannKind. “We are focused on scaling two commercial launches while supporting three programs in IPF. Furoscix ReadyFlow is off to an exceptionally strong start, and we believe Furoscix will generate more revenue in the fourth quarter than it did in the first half of 2026. ReadyFlow significantly expands the opportunity ahead and reinforces our conviction that Furoscix can be transformational for MannKind and the patients we serve.”

 

Business Update

Commercial Products

Furoscix

•
Furoscix® generated $22.4 million in net revenue for the third quarter of 2026, with Furoscix ReadyFlow shipments commencing in mid-September
•
Approximately 75% of Furoscix shipments transitioned to ReadyFlow by late October, demonstrating rapid adoption following launch
•
Achieved record monthly prescribers and prescriptions in September, reflecting continued growth in Furoscix utilization

 

Afrezza

•
Afrezza® generated $19.3 million in net sales for the third quarter of 2026
•
Total prescriptions increased approximately 17% compared with Q2 2026, driven by strong early uptake following the pediatric launch
•
All 60 priority pediatric institutions have prescribed Afrezza, with approximately 2,000 pediatric patients treated since launch

 

Development

Nintedanib DPI (MNKD-201)

•
Positive Phase 1b INFLO-1 results demonstrated tolerability of nintedanib DPI, validating the Technosphere® DPI platform in IPF
•
Advancing MNKD-201 into global Phase 2 trial

 

Ralinepag DPI (MNKD-1501)

•
Formulation work completed; United Therapeutics plans to pursue clinical development
•
Anticipate earning $15 million in milestone payments in 2027

 

Inhaled GLP-1 Program

•
Entered into a licensing and collaboration agreement with Rose Pharma to develop an inhaled rapid-acting, short-duration GLP-1 for weight management

 

Corporate Update

•
Cash, cash equivalents and investments as of September 30, 2026, totaled $96.6 million
•
Closed $50 million private placement on July 24, 2026; proceeds funded the $45 million CVR payment triggered by the FDA approval of Furoscix ReadyFlow

 

 

 

 

 


 

 

Third Quarter 2026 Financial Results

 

Revenues

 

 

 

Three Months
Ended September 30,

 

 

 

2026

 

 

2025

 

 

$ Change

 

 

% Change

 

Revenues

 

(Dollars in thousands)

 

Afrezza

 

 

19,349

 

 

 

18,493

 

 

 

856

 

 

 

5

%

Furoscix

 

 

22,376

 

 

 

—

 

 

 

22,376

 

 

N/A

 

V-Go

 

 

3,277

 

 

 

3,812

 

 

 

(535

)

 

 

(14

%)

Collaborations and services

 

 

19,405

 

 

 

26,506

 

 

 

(7,101

)

 

 

(27

%)

Royalties

 

 

37,463

 

 

 

33,319

 

 

 

4,144

 

 

 

12

%

Total revenues

 

$

101,870

 

 

$

82,130

 

 

$

19,740

 

 

 

24

%

 

Total revenues for the third quarter of 2026 increased compared to the same period in the prior year primarily due to the addition of Furoscix to our product portfolio following the October 2025 acquisition of scPharma, as well as an increase in revenue from royalties. The increase in royalties was due to UT’s increase in net revenue from sales of Tyvaso DPI. The increase in total revenue was partially offset by a decrease in revenue from collaborations and services which was primarily attributable to decreased product sold to UT. UT provides notice of their subsequent year purchase quantity on or prior to October 15th of each year and quarterly revenue fluctuations reflect delivery timing rather than changes in annual order volume.

 

Operating Expenses and Other Financial Highlights

 

Cost of goods sold – commercial, excluding amortization of acquired intangible assets, was $11.2 million for the three months ended September 30, 2026, compared to $4.5 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. The Furoscix on-body infusor has a lower gross margin percentage than Afrezza which resulted in a decrease in gross margin in the current period.

 

Research and development expenses were $14.4 million for the three months ended September 30, 2026, compared to $14.1 million for the same period in 2025, an increase of 2%.
The increase was primarily attributable to the development of Furoscix ReadyFlow, higher personnel costs following the acquisition of scPharma, and increased clinical development costs for MNKD-201. These increases were 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.

 

Selling, general and administrative expenses were $61.4 million for the three months ended September 30, 2026, compared to $29.1 million for the same period in 2025, an increase of 111%.
The increase was primarily attributable to costs associated with the promotion and support of Furoscix, which was acquired from scPharma in October 2025, expansion of our field-based teams, and launch activities related to Furoscix ReadyFlow and the pediatric indication for Afrezza.

 

Nine Months Ended September 30, 2026

 

Revenues

 

 

 

Nine Months
Ended September 30,

 

 

 

2026

 

 

2025

 

 

$ Change

 

 

% Change

 

Revenues

 

(Dollars in thousands)

 

Afrezza

 

 

51,643

 

 

 

51,709

 

 

 

(66

)

 

 

(0

%)

Furoscix

 

 

60,061

 

 

 

—

 

 

 

60,061

 

 

N/A

 

V-Go

 

 

9,188

 

 

 

12,023

 

 

 

(2,835

)

 

 

(24

%)

Collaborations and services

 

 

77,941

 

 

 

78,727

 

 

 

(786

)

 

 

(1

%)

Royalties

 

 

102,583

 

 

$

94,552

 

 

$

8,031

 

 

 

8

%

Total revenues

 

$

301,416

 

 

$

237,011

 

 

$

64,405

 

 

 

27

%

 

Total revenues for the nine months ended September 30, 2026 increased compared to the same period in the prior year due to the addition of Furoscix to our product portfolio following the October 2025 acquisition of scPharma, as well as an increase in royalties. 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 $33.1 million for the nine months ended

 


 

September 30, 2026, compared to $12.9 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. The Furoscix on-body infusor has a lower gross margin percentage than Afrezza which resulted in a decrease in gross margin in the current period.

 

Research and development expenses were $49.6 million for the nine months ended September 30, 2026, compared to $38.8 million for the same period in 2025, an increase of 28%.
The increase was primarily attributable to the development of Furoscix ReadyFlow, higher personnel costs following the acquisition of scPharma, and increased clinical development costs for MNKD-201. These increases were 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.

 

Selling, general and administrative expenses were $173.8 million for the nine months ended September 30, 2026, compared to $85.7 million for the same period in 2025, an increase of 103%.
The increase was primarily attributable to costs associated with the promotion and support of Furoscix, expansion of our field-based teams, and launch activities related to Furoscix ReadyFlow and the pediatric indication for Afrezza.

 

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 can be accessed live via the Events & Presentations section of MannKind’s Investor Relations website. A replay will remain available in the same location for approximately 90 days following the conference call.

 

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 anticipated growth potential for Furoscix, including as a major commercial brand; the development plans for ralinepag DPI and the expected timing for milestone payments related thereto; the potential benefits of and opportunities for MannKind’s products and product candidates; and expectations regarding MannKind’s ongoing and planned clinical trials and nonclinical studies, including the ongoing Phase 2 INFLO-2 trial. 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 September 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, MANNKIND, and V-GO are registered trademarks, and Furoscix ReadyFlow is a trademark 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 September 30,

 

 

Nine Months
Ended September 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

 

 

(In thousands except per share data)

 

Revenues:

 

 

 

 

 

 

 

 

 

 

 

 

Commercial product sales

 

$

45,002

 

 

$

22,305

 

 

$

120,892

 

 

$

63,732

 

Collaborations and services

 

 

19,405

 

 

 

26,506

 

 

 

77,941

 

 

 

78,727

 

Royalties

 

 

37,463

 

 

 

33,319

 

 

 

102,583

 

 

 

94,552

 

Total revenues

 

 

101,870

 

 

 

82,130

 

 

 

301,416

 

 

 

237,011

 

Expenses:

 

 

 

 

 

 

 

 

 

 

 

 

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

 

 

11,213

 

 

 

4,498

 

 

 

33,130

 

 

 

12,873

 

Cost of revenue – collaborations and services

 

 

12,299

 

 

 

15,705

 

 

 

37,393

 

 

 

45,414

 

Research and development

 

 

14,360

 

 

 

14,063

 

 

 

49,592

 

 

 

38,760

 

Selling, general and administrative

 

 

61,412

 

 

 

29,088

 

 

 

173,801

 

 

 

85,724

 

Amortization of acquired intangible assets

 

 

5,160

 

 

 

—

 

 

 

13,895

 

 

 

—

 

(Gain) loss on foreign currency transaction

 

 

(391

)

 

 

(120

)

 

 

(2,195

)

 

 

7,752

 

Total expenses

 

 

104,053

 

 

 

63,234

 

 

 

305,616

 

 

 

190,523

 

(Loss) income from operations

 

 

(2,183

)

 

 

18,896

 

 

 

(4,200

)

 

 

46,488

 

Other income (expense):

 

 

 

 

 

 

 

 

 

 

 

 

Interest income

 

 

1,090

 

 

 

2,628

 

 

 

3,541

 

 

 

6,416

 

Interest expense

 

 

(7,642

)

 

 

(1,364

)

 

 

(27,015

)

 

 

(6,294

)

Interest expense on liability for sale of future royalties

 

 

(501

)

 

 

(3,514

)

 

 

(3,573

)

 

 

(10,564

)

Interest expense on financing liability

 

 

(2,434

)

 

 

(2,456

)

 

 

(7,241

)

 

 

(7,299

)

Impairment of available-for-sale investment

 

 

—

 

 

 

(6,409

)

 

 

—

 

 

 

(6,409

)

Loss on settlement of debt

 

 

—

 

 

 

—

 

 

 

(917

)

 

 

—

 

Other expense, net

 

 

(11,503

)

 

 

—

 

 

 

(19,271

)

 

 

—

 

Total other expense, net

 

 

(20,990

)

 

 

(11,115

)

 

 

(54,476

)

 

 

(24,150

)

(Loss) income before income tax expense (benefit)

 

 

(23,173

)

 

 

7,781

 

 

 

(58,676

)

 

 

22,338

 

Income tax expense (benefit)

 

 

51

 

 

 

(204

)

 

 

198

 

 

 

527

 

Net (loss) income

 

$

(23,224

)

 

$

7,985

 

 

$

(58,874

)

 

$

21,811

 

Net (loss) income per share – basic

 

$

(0.07

)

 

$

0.03

 

 

$

(0.19

)

 

$

0.07

 

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

 

 

320,182

 

 

 

306,806

 

 

 

312,722

 

 

 

305,093

 

Net (loss) income per share – diluted

 

$

(0.07

)

 

$

0.03

 

 

$

(0.19

)

 

$

0.07

 

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

 

 

320,182

 

 

 

311,638

 

 

 

312,722

 

 

 

313,339

 

 

 


 

 

 

MANNKIND CORPORATION AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS

 

 

 

September 30, 2026

 

 

December 31, 2025

 

 

 

(In thousands except share
and per share data)

 

ASSETS

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

41,276

 

 

$

74,882

 

Short-term investments

 

 

55,333

 

 

 

96,464

 

Accounts receivable, net

 

 

41,034

 

 

 

38,367

 

Inventory

 

 

48,469

 

 

 

35,313

 

Prepaid expenses and other current assets

 

 

54,364

 

 

 

46,553

 

Total current assets

 

 

240,476

 

 

 

291,579

 

Restricted cash

 

 

749

 

 

 

745

 

Property and equipment, net

 

 

86,371

 

 

 

82,423

 

Goodwill

 

 

67,595

 

 

 

67,595

 

Developed technology - Furoscix

 

 

305,877

 

 

 

190,027

 

IPR&D - ReadyFlow Formulation

 

 

—

 

 

 

129,600

 

Other intangible assets

 

 

4,927

 

 

 

5,072

 

Other assets

 

 

16,621

 

 

 

20,129

 

Long-term investments

 

 

—

 

 

 

5,012

 

Total assets

 

$

722,616

 

 

$

792,182

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS' DEFICIT

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

14,383

 

 

$

9,034

 

Accrued expenses and other current liabilities

 

 

59,593

 

 

 

64,628

 

Liability for sale of future royalties – current

 

 

14,573

 

 

 

14,298

 

Financing liability – current

 

 

10,565

 

 

 

10,328

 

Deferred revenue – current

 

 

9,410

 

 

 

15,331

 

Contingent consideration – current

 

 

—

 

 

 

21,132

 

Senior convertible notes – current

 

 

—

 

 

 

36,280

 

Total current liabilities

 

 

108,524

 

 

 

171,031

 

Liability for sale of future royalties – long term

 

 

130,026

 

 

 

136,985

 

Financing liability – long term

 

 

92,231

 

 

 

93,092

 

Deferred revenue – long term

 

 

34,809

 

 

 

39,977

 

Recognized loss on purchase commitments – long term

 

 

63,720

 

 

 

65,952

 

Operating lease liability

 

 

9,177

 

 

 

10,689

 

Milestone liabilities

 

 

1,580

 

 

 

2,003

 

Term loan

 

 

319,447

 

 

 

318,361

 

Other long term liabilities

 

 

368

 

 

 

—

 

Contingent consideration – long term

 

 

—

 

 

 

5,114

 

Total liabilities

 

 

759,882

 

 

 

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 September 30, 2026 or December 31, 2025

 

 

—

 

 

 

—

 

Common stock, $0.01 par value – 800,000,000 shares authorized;
  321,633,894 and 307,832,587 shares issued and outstanding as of
  September 30, 2026 and December 31, 2025, respectively

 

 

3,216

 

 

 

3,078

 

Additional paid-in capital

 

 

3,214,437

 

 

 

3,141,741

 

Accumulated other comprehensive (loss) income

 

 

(88

)

 

 

115

 

Accumulated deficit

 

 

(3,254,831

)

 

 

(3,195,956

)

Total stockholders' deficit

 

 

(37,266

)

 

 

(51,022

)

Total liabilities and stockholders' deficit

 

$

722,616

 

 

$

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 September 30,

 

 

Nine Months
Ended September 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

 

$

(23,224

)

 

$

(0.07

)

 

$

7,985

 

 

 

0.03

 

 

$

(58,874

)

 

$

(0.19

)

 

$

21,811

 

 

$

0.07

 

Non-GAAP adjustments:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Stock compensation

 

 

6,444

 

 

 

0.02

 

 

 

4,318

 

 

 

0.01

 

 

 

23,125

 

 

 

0.07

 

 

 

17,223

 

 

 

0.06

 

Interest expense on liability for sale of future royalties

 

 

501

 

 

 

0.00

 

 

 

3,514

 

 

 

0.01

 

 

 

3,573

 

 

 

0.01

 

 

 

10,564

 

 

 

0.03

 

Sold portion of royalty revenue (1)

 

 

(3,746

)

 

 

(0.01

)

 

 

(3,332

)

 

 

(0.01

)

 

 

(10,258

)

 

 

(0.03

)

 

 

(9,455

)

 

 

(0.03

)

(Gain) loss on foreign currency transaction

 

 

(391

)

 

 

0.00

 

 

 

(120

)

 

 

0.00

 

 

 

(2,195

)

 

 

(0.01

)

 

 

7,752

 

 

 

0.03

 

Amortization of intangible assets acquired

 

 

5,160

 

 

 

0.01

 

 

 

—

 

 

 

—

 

 

 

13,895

 

 

 

0.05

 

 

 

—

 

 

 

—

 

Expense related to contingent consideration

 

 

11,641

 

 

 

0.04

 

 

 

—

 

 

 

—

 

 

 

19,409

 

 

 

0.07

 

 

 

—

 

 

 

—

 

Loss on settlement of debt

 

 

—

 

 

 

—

 

 

 

—

 

 

 

—

 

 

 

917

 

 

 

0.00

 

 

 

—

 

 

 

—

 

Acquisition related expenses(2)

 

 

—

 

 

 

—

 

 

 

3,673

 

 

 

0.01

 

 

 

—

 

 

 

—

 

 

 

3,673

 

 

 

0.01

 

Impairment loss on available-for-sale investment

 

 

—

 

 

 

—

 

 

 

6,409

 

 

 

0.02

 

 

 

—

 

 

 

—

 

 

 

6,409

 

 

 

0.02

 

Non-GAAP adjusted net (loss) income

 

$

(3,615

)

 

$

(0.01

)

 

$

22,447

 

 

$

0.07

 

 

$

(10,408

)

 

$

(0.03

)

 

$

57,977

 

 

$

0.19

 

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

 

 

320,182

 

 

 

 

 

 

306,806

 

 

 

 

 

 

312,722

 

 

 

 

 

 

305,093

 

 

 

 

 

(1)
Represents the non-cash portion of the 1% royalty on net sales of Tyvaso DPI earned during the three and nine months ended September 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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