A Study to Evaluate Safety, Tolerability and Pharmacokinetics of MNKD-201 in Patients With Idiopathic Pulmonary Fibrosis

Completed · Phase 1 · Has a placebo group

Conditions studied: Idiopathic Pulmonary Fibrosis (IPF)

In brief

MKC-NI-002 is a Phase 1b, randomized, double-blind, placebo-controlled study of nintedanib inhalation powder (MNKD-201) in patients with Idiopathic Pulmonary Fibrosis (IPF). The trial consists of Multiple Ascending Doses (MAD) with the primary objective to evaluate safety, tolerability and pharmacokinetics (PK) of MNKD-201 compared to placebo in patients with IPF.

Key facts

Study ID: NCT07344558
Run by: Mannkind Corporation
People needed: 27
Starts: 2025-12-22
Expected to finish: 2026-06-17
Last updated by the study team: 2026-07-22

Who can join

Age: 40 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Is ≥40 to ≤85 years of age at the time of signing the informed consent form.
Diagnosis of IPF
Either treatment-naive or is currently on background pirfenidone or nerandomilast on a stable dose for at least 3 months prior to Screening.
Has FVC >45% of predicted of normal, as determined by the central spirometry reader, during Screening.
DLCO corrected for hemoglobin [Visit 1] ≥40% of predicted of normal, within 12 months of Screening. If no historical DLCO is available prior to Screening, this is to be done during Screening and read locally.
Has a body weight >40 kg (>88 lbs.) at Screening.
For female participants of childbearing potential, agreement to use acceptable birth control
For male participants who can father a child and are having intercourse with females of childbearing potential, agreement to use a protocol-recommended method of contraception
Is capable of performing spirometry, as required by the study procedures and ATS guidelines.
CT chest within 2 years of Screening, consistent with an IPF diagnosis, per investigator assessment.

You may not qualify if…

Known explanation for interstitial lung disease, including but not limited to radiation, sarcoidosis, hypersensitivity pneumonitis, and bronchiolitis obliterans organizing pneumonia.
Diagnosis of any connective tissue disease, including but not limited to scleroderma/systemic sclerosis, polymyositis/dermatomyositis, systemic lupus erythematosus, and rheumatoid arthritis, regardless of whether or not it is presumed to be related to their pulmonary fibrosis diagnosis.
Major extrapulmonary physiological restriction (e.g., chest wall abnormality, large pleural effusion), as determined by the investigator.
Significant Cardiovascular diseases
Recent systemic infection within 4 weeks before the Screening visit or symptomatic viral or bacterial infection at time of Screening.
Prior hospitalization for confirmed coronavirus disease 2019 (COVID-19), acute exacerbation of IPF or any lower respiratory tract infection within 3 months of Screening.
Has a history of asthma, with the exception of resolved childhood asthma.
Has known obstructive lung disease
Alanine aminotransferase (ALT), aspartate aminotransferase (AST), or total bilirubin >1.5 times the upper limit of normal (ULN) during Screening.
Advanced liver and kidney function.
Current or recent (within 30 days of Screening) use of nintedanib.
Use of prednisone >10 mg/day within 1 month prior to Screening, or other significant immunosuppression
Active lung cancer (primary or metastatic) or any cancer requiring chemotherapy or radiation therapy within 3 years, except appropriately treated non-melanoma skin cancer, localized non-malignant prostate cancer, or in situ carcinoma of uterine cervix.
Has participated in another clinical study of a new chemical entity, new device, or a prescription medicine within the 1 month before Screening
Current alcohol, medication, or illicit drug abuse
Has lost more than 400 mL blood, e.g., as a blood donor, or donor of blood products, during the 3 months prior to Screening.
Has received a live vaccine within the 3 months prior to the first dose of study drug.
Smokes (any substance including electronic cigarettes and marijuana) within 3 months prior to Screening or is an ex-cigarette smoker who gave up <1 year ago.
Has oxygen requirement of > 6 liters/min at rest.

Where it is running

VALDI — Fresno, California, United States
Palmtree Clinical Research — Palm Springs, California, United States
Innova Pharma Research — Doral, Florida, United States
New Life Medical Research — Hialeah, Florida, United States
New Access Research and Medical Services — Miami, Florida, United States
Southeastern Research Center — Winston-Salem, North Carolina, United States
Low Country Research — Charleston, South Carolina, United States
Metroplex Pulmomary & Sleep Center — McKinney, Texas, United States
Pulmonary Medicine Consultants — McKinney, Texas, United States

Full record on ClinicalTrials.gov

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