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Study on Doses of Inhaled ALX1 in Adults With Bronchiectasis

23 juli 2026 uppdaterad av: 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.

Studieöversikt

Status

Har inte rekryterat ännu

Betingelser

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Beräknad)

28

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

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

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Placebo-jämförare: Placebo
Dose Formulation: Solution for inhalation Dose Strength: 0.9% sodium chloride Route of Administration: Inhalation via nebulizer
Experimentell: ALX1
Dose Formulation: Solution for inhalation Dose Strength: 28 mg/mL Route of Administration: Inhalation via nebulizer

Vad mäter studien?

Primära resultatmått

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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of TEAEs
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Incidence of SAEs
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal vital signs
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal Laboratory parameters
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal ECG readings
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal SpO2
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)
Proportion of participants with abnormal Spirometry Value
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: From Day 1 to Day 14 (EOT visit)
From Day 1 to Day 14 (EOT visit)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 september 2026

Primärt slutförande (Beräknad)

31 mars 2027

Avslutad studie (Beräknad)

31 mars 2027

Studieregistreringsdatum

Först inskickad

23 juli 2026

Först inskickad som uppfyllde QC-kriterierna

23 juli 2026

Första postat (Faktisk)

28 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

28 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

23 juli 2026

Senast verifierad

1 juli 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • VST-201

Plan för individuella deltagardata (IPD)

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NEJ

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

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Nej

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