- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07679893
Phase 2 Clinical Trial of MNKD-201 (Nintedanib Dry Powder Inhalation) in Patients With Idiopathic Pulmonary Fibrosis (INFLO-2)
9. September 2026 aktualisiert von: Mannkind Corporation
A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Clinical Trial of the Efficacy and Safety of MNKD-201 (Nintedanib Dry Powder Inhalation) in Patients With Idiopathic Pulmonary Fibrosis Followed by an Open-Label Extension
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 BID, 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.
Studienübersicht
Status
Rekrutierung
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Geschätzt)
153
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Wassim Fares, MD, SVP, Therapeutic Area Head, Orphan Lung Disease, MD
- Telefonnummer: 203-796-3407
- E-Mail: wfares@mannkindcorp.com
Studienorte
-
-
Ontario
-
Windsor, Ontario, Kanada, N8X1T3
- Rekrutierung
- Trial Management Group Inc
-
Kontakt:
- Syed Anees
- Telefonnummer: 416-929-7717
- E-Mail: aneesresearch@yahoo.com
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
Inclusion Criteria:
- 40-80 years old when signing consent and entering screening.
- Diagnosed with IPF based on current ATS/ERS/JRS/ALAT guidelines.
- Either new to treatment or on a stable dose of pirfenidone and/or nerandomilast for at least 3 months before screening.
- Weighs more than 40 kg (88 lb) at screening.
- Women who can become pregnant:
- Must have a negative pregnancy test at screening.
- Must use an approved birth control method from screening until at least 1 month after the last study dose.
- Men who can father a child and are sexually active with women who can become pregnant:
- Must use an approved birth control method during treatment and for at least 3 months after the last study dose.
- Must not donate sperm during treatment and for at least 3 months after the last study dose.
- Willing to follow all study rules and restrictions.
- Willing and able to attend study visits and complete study procedures.
- Able to perform spirometry (lung function testing) as required by the study.
Exclusion Criteria:
- Has a lung disease caused by something other than IPF.
- Has a connective tissue or autoimmune disease (such as lupus, scleroderma, or rheumatoid arthritis).
- Has another condition that significantly affects breathing.
- Has serious heart or blood vessel disease.
- Has a recent or current infection.
- Was recently hospitalized for COVID-19, an IPF flare-up, or a lung infection.
- Has a history of asthma (except childhood asthma that has resolved).
- Has another medical condition or abnormal test result that may affect study participation or safety.
- Cannot perform high-quality spirometry testing.
- Has obstructive lung disease.
- Has abnormal liver function tests.
- Has moderate to severe liver disease.
- Has severe kidney disease.
- Has recently used high-dose steroids or other immune-suppressing medications.
- Has active cancer or recent cancer treatment.
- Is on, or expected to be added to, a transplant list.
- Had major surgery recently or has planned procedures that could interfere with the study.
- Has had a severe reaction to nintedanib or cannot take nintedanib safely.
- Has recently used certain medications that may interact with the study drug.
- Is currently using, or plans to use, prohibited medications during the study.
- Has recently participated in another clinical trial.
- Has current alcohol or drug abuse issues.
- Donated a significant amount of blood recently.
- Received a live vaccine recently.
- Currently smokes, recently smoked, or quit smoking less than 1 year ago.
- Requires more than 6 L/min of oxygen while at rest.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Nintedanib DPI 2X day 1st dose
Inhalable
|
Nintedanib DPI is a dry powder nintedanib formulation for oral inhalation.
|
|
Placebo-Komparator: Placebo 2X day 1st dose
Inhalable
|
Placebo oral inhalation powder
|
|
Experimental: Nintedanib DPI 2X day 2nd dose
2nd dose
|
Nintedanib DPI is a dry powder nintedanib formulation for oral inhalation.
|
|
Placebo-Komparator: Placebo 2X day 2nd dose
2nd dose
|
Placebo oral inhalation powder
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety and Efficacy
Zeitfenster: From enrollment to the end of randomized treatment at 12 weeks
|
Safety and tolerability of different doses and to confirm an optimal dose of Nintedanib Dry Powder Inhalation (DPI)
|
From enrollment to the end of randomized treatment at 12 weeks
|
|
Events of clinical bronchospasm
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Events of clinical bronchospasm (e.g., treatment-emergent adverse event [TEAE] of wheezing or chest tightness immediately after inhalation)
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
FEV1 change
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Change in forced expiratory volume in 1 second (FEV1) (mL)
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
Spirometry Change
Zeitfenster: enrollment to end of open label at 36 weeks
|
Change in FEV1/forced vital capacity (FVC) ratio
|
enrollment to end of open label at 36 weeks
|
|
Study Drug Discontinuation
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Rate of study drug discontinuations
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
Study Drug Dose Reductions
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Rate of study drug dose reductions
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
Adverse Events
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Rate of TEAEs
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
Related Adverse Events
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Rate of treatment-related adverse events (TRAEs)
|
From enrollment to the end of open-label treatment at 36 weeks
|
|
Serious Adverse Events
Zeitfenster: From enrollment to the end of open-label treatment at 36 weeks
|
Rate of serious adverse events (SAEs)
|
From enrollment to the end of open-label treatment at 36 weeks
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Efficacy of Nintedanib DPI
Zeitfenster: From enrollment to the end of randomized treatment at 12 weeks
|
To assess a potential efficacy signal of different doses of Nintedanib DPI over 12 weeks in patients with IPF.
|
From enrollment to the end of randomized treatment at 12 weeks
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
15. Mai 2026
Primärer Abschluss (Geschätzt)
30. Dezember 2027
Studienabschluss (Geschätzt)
1. Juni 2028
Studienanmeldedaten
Zuerst eingereicht
18. Juni 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
25. Juni 2026
Zuerst gepostet (Tatsächlich)
1. Juli 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
14. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
9. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- MKC-NI-003
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Ja
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Ja
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