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NCT07679893 · ClinicalTrials.gov registry record · Phase 2

Phase 2 Clinical Trial of MNKD-201 (Nintedanib Dry Powder Inhalation) in Patients With Idiopathic Pulmonary Fibrosis

A Phase 2 study, sponsored by Mannkind Corporation.

Not yet
Registry status
Phase 2
Development phase
210
Enrollment target

NCT07679893: Clinical Trial Phase 2 study, sponsored by Mannkind Corporation.

NCT07679893 is a Phase 2 study that has not yet begun recruiting, run by Mannkind Corporation. The registered enrollment target is 210 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07679893, a Phase 2 study, has not yet begun recruiting, sponsored by Mannkind Corporation.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
210 participants
Enrollment target

Study Summary

This trial is a randomized, double-blind, placebo-controlled study evaluating the safety and preliminary efficacy of inhaled Nintedanib Dry Powder Inhalation (DPI) in adults with idiopathic pulmonary fibrosis (IPF). Participants are randomized to receive either 2 mg QID, 4 mg BID, or matching placebo for 12 weeks, followed by a 24-week open-label extension in which all participants receive active treatment. The primary focus is on safety-particularly bronchospasm events, lung function changes (FEV1, FEV1/FVC), and adverse event rates and assessing the effectiveness of nintedanib DPI in treating IPF.

Interventions

  • DRUG Placebo
  • DRUG Nintedanib Dry Powder Inhalation

Trial Details

FieldValue
Enrollment Target 210 participants
Start Date 2026-06-30
Est. Completion 2028-12
Phase Phase 2
Mannkind Corporation

42 total trials

What is known before NCT07679893 opens enrollment

NCT07679893 is an interventional study that assigns participants to a tested intervention. The registered 210 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT07679893 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07679893 about?

NCT07679893 is a clinical study titled "Phase 2 Clinical Trial of MNKD-201 (Nintedanib Dry Powder Inhalation) in Patients With Idiopathic Pulmonary Fibrosis". This trial is a randomized, double-blind, placebo-controlled study evaluating the safety and preliminary efficacy of inhaled Nintedanib Dry Powder Inhalation (DPI) in adults with idiopathic pulmonary fibrosis (IPF). Participants are randomized to receive either 2 mg QID, 4 mg BID, or matching placeb...

What is the current status of trial NCT07679893?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 210 participants. The study started on 2026-06-30. Estimated completion is 2028-12.

What interventions are being tested in trial NCT07679893?

The interventions under investigation include: Placebo (DRUG), Nintedanib Dry Powder Inhalation (DRUG).

Who is sponsoring clinical trial NCT07679893?

This trial is sponsored by Mannkind Corporation, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07679893's enrollment target sits among peer trials

210 290th of 2000 higher than 1,707 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07679893, the US trial registry maintained by the National Library of Medicine. NCT07679893 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.