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Study on Doses of Inhaled ALX1 in Adults With Bronchiectasis

23. juli 2026 opdateret af: Vast Therapeutics

A Phase 2a, Placebo-Controlled, Single-Blind, Dose Range-Finding Study of Inhaled ALX1 in Adults With Bronchiectasis

This study will evaluate the safety and effects of ALX1, an inhaled investigational treatment, in adults with bronchiectasis. Participants will receive either ALX1 or a placebo (a treatment with no active medicine) for 14 days. The study will compare different dose levels of ALX1 to help identify appropriate doses for future research based on safety, tolerability, and changes in predictive biomarkers.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

This is a Phase 2a, multicentre, placebo-controlled, single-blind, dose range-finding study will assess the safety, tolerability, pharmacodynamics (PD), and preliminary efficacy of inhaled ALX1 or placebo administered for 14 days in adult participants with bronchiectasis. 28 participants will be enrolled and assigned to one of four cohorts. The total duration of study participation will be up to 53 days, including Pre-screening and Screening of approximately 32 days, a Treatment Period of approximately 14 days, and a Follow-up of approximately 1 day following the last dose.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

28

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Current sputum producer with a history of chronic expectoration that, in the opinion of the Investigator, will be able to continue to reliably provide sputum throughout the study.
  • Confirmed diagnosis of BE per high-resolution computed tomography (HRCT) prior to Screening due to any of the following: NCFB, CF, primary ciliary dyskinesia, or COPD.
  • Clinical history consistent with BE (cough, daily chronic sputum production, and/or recurrent respiratory infections).
  • FEV1 ≥ 40% of predicted values at Screening.
  • Able to reproducibly perform spirometry manoeuvres (i.e., able to perform at least 3 acceptable forced expiratory curves based on the PI's assessment).
  • History of at least one exacerbation treated with a course of antibiotics (inhaled, oral or intravenous [IV]) within the 24 months prior to Screening
  • Woman of childbearing potential (WOCBP) or fertile man (see definitions in Section 5.3) agrees to use an acceptable method of contraception from the start of Screening until 90 days after the last dose of IP.

Exclusion Criteria:

  • Negative sputum NEATstik result for neutrophil elastase at Pre-screening.
  • History of Burkholderia cepacia complex within 2 years prior to Pre-screening and/or detection of any Burkholderia spp. in sputum culture or by polymerase chain reaction (PCR) at Screening.
  • History of Aspergillus fumigatus requiring treatment within 12 months prior to Pre-screening.
  • History of non-tuberculosis mycobacteria (NTM) infection requiring treatment within 12 months prior to Screening, or detection of one or more NTM species in sputum by PCR at Screening.
  • History of bronchospasm with inhaled antibiotics or hypertonic saline.
  • Haemoptysis exceeding 50 mL of blood from the respiratory tract at any time within 30 days prior to IP administration (Day 1).
  • Initiated macrolide therapy within 90 days before Screening. Existing stable maintenance with inhaled macrolides is permitted if initiated more than 90 days prior to Screening.
  • Received inhaled anti-pseudomonal therapy within the last 14 days before Pre-screening. Must be willing to refrain from use of inhaled anti-pseudomonal therapy during the study until completion of the Follow-up video/telephone call.
  • Received oral antibiotics other than macrolide within 30 days prior to Screening. Must be willing to refrain from use of oral antibiotics during the study until completion of the Follow-up video/telephone call.
  • Received IV antibiotics within 60 days prior to Screening
  • Initiation of, or increase in the dose of, inhaled corticosteroids within 90 days prior to Screening. Note: participants may be taking stable inhaled corticosteroids at the time of enrolment but must have initiated treatment more than 90 days prior to Screening
  • Started any of the following muco-corrective therapies (e.g., nebulised saline, N-acetyl cysteine, Pulmozyme®, etc.) within 30 days prior to Screening. Maintenance with these muco-corrective therapies is permitted if initiated 30 days prior to Screening.
  • Any of the following laboratory abnormalities at Screening:

    1. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 × upper limit of normal (ULN)
    2. Creatinine > 1.5 × ULN
  • QT interval corrected by Fridericia's formula (QTcF) interval > 450 ms for males or > 470 ms for females at Screening, or history of prolonged QT syndrome. PR interval < 200 ms at Screening. Out-of-range values may be repeated twice for confirmation. The mean QTcF and PR intervals of the triplicate ECG recordings will be used to determine qualification.
  • Positive test for hepatitis C antibody (HCV), hepatitis B surface antigen (HBsAg), or human immunodeficiency virus (HIV) antibody at Screening

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Dose Formulation: Solution for inhalation Dose Strength: 0.9% sodium chloride Route of Administration: Inhalation via nebulizer
Eksperimentel: ALX1
Dose Formulation: Solution for inhalation Dose Strength: 28 mg/mL Route of Administration: Inhalation via nebulizer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Proportion of participants with a metHb value ≥ 5% per dose level
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Incidence of TEAEs
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Incidence of SAEs
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal vital signs
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal Laboratory parameters
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal ECG readings
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal SpO2
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal Spirometry Value
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Mean change in sputum inflammatory biomarkers per dose level
Tidsramme: From Day 1 to Day 14 (EOT visit)
Active neutrophil elastase, IL-1β, IL-6, IL-8, and TNF-alpha biomarkers assessed via quantitative immunoassay
From Day 1 to Day 14 (EOT visit)
Mean change in total bacterial load of pathogens per dose level
Tidsramme: From Day 1 to Day 14 (EOT visit)
Assessed by sputum culture and quantitative polymerase chain reaction (qPCR)
From Day 1 to Day 14 (EOT visit)
Proportion of participants achieving a microbiological culture of pathogens change of at least 1-log CFU/g per dose level
Tidsramme: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. september 2026

Primær færdiggørelse (Anslået)

31. marts 2027

Studieafslutning (Anslået)

31. marts 2027

Datoer for studieregistrering

Først indsendt

23. juli 2026

Først indsendt, der opfyldte QC-kriterier

23. juli 2026

Først opslået (Faktiske)

28. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

28. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • VST-201

Plan for individuelle deltagerdata (IPD)

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INGEN

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