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MNKD

MANNKIND CORP

Pharmaceutical preparations·Commercial·Danbury, CT, United States·CEO: Dr. Michael E. Castagna Pharm.D.
CardiovascularMetabolicRespiratory

MNKD evidence brief

What we can confirm

BioSniper Score:
4.0 / 10
Market Cap:
$1.21B
Lead Asset:
afrezza (Phase 4)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $1.21B · Lead Asset: afrezza (Phase 4)
BioSniper AIPage evidence connected

Prepared research question

What matters most for MNKD—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · MNKD

MANNKIND CORP (MNKD) is a biopharmaceutical company focused on cardiometabolic and orphan lung diseases, with commercial products including Afrezza (inhaled insulin) and FUROSCIX, and a pipeline of inhaled therapies for pulmonary fibrosis and nontuberculous mycobacterial infection.

Key risk: High debt burden

4.0/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$1.21B

Cash Runway

—

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 6 clinical trials · 1 catalyst · 1 FDA decision for MANNKIND CORP.

AI OverviewAI overview is shown in English only.

MANNKIND CORP (MNKD) is a biopharmaceutical company focused on cardiometabolic and orphan lung diseases, with commercial products including Afrezza (inhaled insulin) and FUROSCIX, and a pipeline of inhaled therapies for pulmonary fibrosis and nontuberculous mycobacterial infection.

  • Cash & equivalents of $52.9M as of 2026-06-30 [sec].
  • Total revenue of $109.4M and net income of -$19.0M as of 2026-06-30 [sec].
  • Shareholders' equity of -$67.2M and total debt of $325.0M as of 2026-06-30 [sec].
  • Commercial products include Afrezza (inhaled insulin) and FUROSCIX (for fluid overload) [sec · filed 2026-04-07].
  • Pipeline includes MNKD-201 (nintedanib DPI for IPF) in Phase 1b/2 and MNKD-1501 (ralinepag DPI) in collaboration with UT [sec · filed 2026-04-07].

What works

  • Revenue growth trajectory: Q1 2026 total revenues of $90.2M, +15% vs. Q1 2025 [news · published 2026-05-06].
  • Multiple near-term regulatory catalysts: Afrezza pediatric PDUFA date May 29, 2026 and FUROSCIX ReadyFlow Autoinjector PDUFA date July 26, 2026 [news · published 2026-05-06].
  • Pipeline expansion through collaboration: In August 2025, announced expansion to formulate MNKD-1501 with UT conducting preclinical and clinical development [sec · filed 2026-04-07].
  • Phase 3 trial (ICoN-1) for MNKD-101 (clofazimine inhalation suspension for NTM) achieved interim enrollment target ahead of schedule [news · published 2025-11-05].

What to weigh

  • Negative net income of -$19.0M as of 2026-06-30 [sec].
  • Negative shareholders' equity of -$67.2M as of 2026-06-30 [sec].
  • High total debt of $325.0M as of 2026-06-30 [sec].
  • Afrezza faces competition from rapid-acting insulin analogs marketed by Eli Lilly, Sanofi, and Novo Nordisk, as well as GLP-1 analog injection products [pipeline].

From the filings

Quoted directly from source documents.

  • Afrezza pediatric PDUFA date

    “Afrezza® pediatric indication PDUFA date May 29, 2026”

    News · May 6, 2026

Catalyst timeline

  • 2042-02-03 · Patent_Expiry · TREPROSTINIL — Patent expiry for NDA214324; may affect market exclusivity for treprostinil products.
Risks & what to watch (4)›

Key risks

  • High debt burden — Total debt of $325.0M as of 2026-06-30 [sec].
  • Negative equity — Shareholders' equity of -$67.2M as of 2026-06-30 [sec].
  • Competitive pressure on Afrezza — Afrezza competes with rapid-acting insulin analogs from Eli Lilly, Sanofi, Novo Nordisk, and GLP-1 analogs [pipeline].
  • Patent expiry risk — Patent expiry for TREPROSTINIL on 2042-02-03 [catalyst].

What to watch

  • Afrezza pediatric PDUFA date May 29, 2026 [news · published 2026-05-06].
  • FUROSCIX ReadyFlow Autoinjector PDUFA date July 26, 2026 [news · published 2026-05-06].
  • MNKD-201 Phase 2 INFLO-2 trial first patient enrollment expected Q2 2026 [news · published 2026-05-06].
  • Patent expiry for TREPROSTINIL on 2042-02-03 [catalyst].

Sources: Catalysts · News · Pipeline · SEC filings · SEC MD&A · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health2.0

Net income -$19M

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth4.6

2 candidates

Catalyst Momentum2.0

1 upcoming, next in ~5591d

Insider Signal1.5

0 buys · 5 sells (180d)

Catalysts

Pipeline

Regulatory

Financials

Short Interest

as of May 1, 2026
% of float
9.7%
Days to cover
5.4
Shares short
29,576,907
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

MNKD short interest

Governance

Frequently asked questions

What is the AI investment thesis for MANNKIND CORP?

MANNKIND CORP (MNKD) is a biopharmaceutical company focused on cardiometabolic and orphan lung diseases, with commercial products including Afrezza (inhaled insulin) and FUROSCIX, and a pipeline of inhaled therapies for pulmonary fibrosis and nontuberculous mycobacterial infection.

What is MANNKIND CORP's lead drug candidate?

MANNKIND CORP's most advanced tracked candidate is afrezza (Phase 4) for Diabetes Mellitus, Type 1; Type 1 Diabetes.

What is MANNKIND CORP's next catalyst?

MANNKIND CORP's next tracked catalyst is a Patent_Expiry event — "Patent_Expiry: NDA214324" — expected February 3, 2042.

Who is the CEO of MANNKIND CORP?

Dr. Michael E. Castagna Pharm.D. is the chief executive officer of MANNKIND CORP (MNKD).

Where is MANNKIND CORP headquartered?

MANNKIND CORP (MNKD) is headquartered in Danbury, CT, United States.

923 companies304,844 SEC filings22,644 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.