Biopharma Transcript

MannKind Corporation MNKD

Nasdaq · Phase 2 · cardio-renal-metabolic · protein/peptide · EDGAR · Updated Oct 24, 2026

MannKind Corporation (Nasdaq: MNKD) is a cardio-renal-metabolic drug developer. Its lead program, Afrezza (insulin human) Inhalation Powder, is in Phase 2 for Diabetes mellitus (adults; label expanded to ages 6 and older May 2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
AfrezzaDiabetes (adult and pediatric ages 6+)protein/peptideApproved
Furoscix (furosemide injection, incl. ReadyFlow autoinjector)Edema in heart failure / chronic kidney diseasedevice-combinationApproved
MNKD-201 (inhaled nintedanib dry powder)Idiopathic pulmonary fibrosissmall moleculePhase 2
MNKD-701 (inhaled bumetanide)Fluid overload (feasibility)small moleculePre-clinical

Recent results and decisions

  1. Aug 5, 2026
    positive Topline Phase 1b INFLO-1 data showed nintedanib DPI was safe and well tolerated in IPF patients, supporting Phase 2 advancement; no efficacy numbers given.Topline data readout of U.S. Phase 1b INFLO-1 demonstrates safety and tolerability in IPF patients Filing
  2. Jul 23, 2026
    approval FDA approved FUROSCIX ReadyFlow on July 23, 2026, an autoinjector delivering IV-equivalent diuretic therapy; commercial availability expected late August.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) Filing
  3. May 29, 2026
    approval FDA approved Afrezza on May 29, 2026 for children and adolescents ages 6 and older with diabetes (pediatric sBLA).Received FDA approval of Afrezza on May 29, 2026 for use in children and adolescents ages 6 and older living with diabetes Filing

5 more on record.

For subscribers

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