MannKind Corporation, a biopharmaceutical company, focuses on the development and commercialization of therapeutic products and services for endocrine and orphan lung diseases in the United States. It offers Afrezza Inhalation Powder, an inhaled insulin used to improve glycemic control in adults with diabetes; the V-Go wearable insulin delivery device, which provides continuous subcutaneous infusion of insulin in adults; and Tyvaso DPI for the treatment of pulmonary arterial hypertension and pulmonary hypertension. The company's product pipeline includes MNKD-101, a nebulized formulation of clofazimine, which is in Phase 3 study, for the treatment of severe chronic and recurrent pulmonary infections, including nontuberculous mycobacterial lung disease; MNKD-201, a dry-powder formulation of nintedanib, which is in phase 1 clinical study, for the treatment of idiopathic pulmonary fibrosis (IPF); MNKD-301, which is in preclinical stage, for cystic fibrosis; and Pediatric Afrezza, which is in phase 3 clinical trial for the treatment of diabetes mellitus. It has collaboration and license agreement with United Therapeutics Corporation for development, regulatory, and commercial activities of Tyvaso DPI; and collaboration agreement with Thirona to evaluate the therapeutic for the treatment of pulmonary fibrosis. Further, the company has supply and distribution agreement with Biomm S.A. for the commercialization of Afrezza in Brazil; license and distribution agreement with Cipla Ltd. for the marketing and distribution of Afrezza in India; and co-promotion agreement with Amphastar for marketing of Baqsimi (glucagon) nasal powder. MannKind Corporation was incorporated in 1991 and is headquartered in Danbury, Connecticut. Show more
Location: 1 Casper Street, Danbury, CT, 06810, United States | Website: https://www.mannkindcorp.com | Industry: Biotechnology | Sector: Healthcare
Market Cap
1.667B
52 Wk Range
$3.38 - $7.07
Previous Close
$5.43
Open
$5.45
Volume
4,130,201
Day Range
$5.42 - $5.68
Enterprise Value
1.529B
Cash
260M
Avg Qtr Burn
N/A
Insider Ownership
1.74%
Institutional Own.
57.00%
Qtr Updated
09/30/25
Drug Pipeline
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
FUROSCIX (furosemide) Details Chronic kidney disease, Kidney disease | Approved Quarterly sales | |
FUROSCIX (furosemide) Details Heart failure | Approved Quarterly sales | |
FUROSCIX (furosemide) Details Heart failure, Chronic kidney disease | Approved Quarterly sales | |
Afrezza® (insulin human) Inhalation Powder Details Diabetes, Type 1 diabetes, Type 2 diabetes | Approved Quarterly sales | |
Tyvaso DPI (Treprostinil Technosphere®) (inhaled treprostinil) Details Pulmonary arterial hypertension, Heart disease | Approved Quarterly sales | |
FUROSCIX ReadyFlow™ Auto-Injector Injection (furosemide) Details Edema in Adults with Chronic Heart Failure (CHF) or Chronic Kidney Disease (CKD) | PDUFA Approval decision | |
Afrezza® (insulin human) Inhalation Powder Details Type 1 diabetes, Diabetes, Type 2 diabetes | PDUFA Approval decision | |
MNKD 201 (nintedanib DPI) Details Lung disease, Idiopathic pulmonary fibrosis | Phase 2 Initiation | |
Clofazimine inhalation suspension (MNKD 101) Details Nontuberculous mycobacterial lung disease, Lung disease | Failed Discontinued |
