Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06529419 · ClinicalTrials.gov registry record · Phase 2

A Dose Range-Finding Study to Assess the Efficacy and Safety of Multiple Dose Levels of AZD8630 in Adults With Uncontrolled Asthma at Risk of Exacerbations

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
537
Enrollment target

NCT06529419: Completed Phase 2 study, sponsored by AstraZeneca.

NCT06529419 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 537 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (304% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06529419, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
537 participants
Enrollment target

Study Summary

A dose range-finding study to assess the efficacy and safety of multiple dose levels of AZD8630 administered via a dry powder inhaler in adults with uncontrolled asthma at risk of exacerbations, receiving medium -to -high dose inhaled corticosteroid (ICS)/long-acting β2-agonist (LABA).

Primary Outcome

The CompEx Asthma is a composite endpoint for exacerbations that captures asthma-worsening episodes based on combination of diary events (worsening in daily PEF, asthma symptoms and rescue medication use) plus severe asthma exacerbation events. Diary events are defined by threshold and slope criteria using the following morning/evening diary variables: * PEF * Asthma symptom score (0 to 3) * Use of rescue medication

Interventions

  • DRUG Placebo
  • DRUG AZD8630
  • DEVICE Inhaler

Trial Details

FieldValue
Enrollment Target 537 participants
Start Date 2024-08-30
Est. Completion 2026-02-04
Phase Phase 2
AstraZeneca

1,285 total trials

What the finished NCT06529419 record still lists

NCT06529419 is an interventional study that assigns participants to a tested intervention. The registered 537 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 (304% higher).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT06529419 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06529419 about?

NCT06529419 is a clinical study titled "A Dose Range-Finding Study to Assess the Efficacy and Safety of Multiple Dose Levels of AZD8630 in Adults With Uncontrolled Asthma at Risk of Exacerbations". A dose range-finding study to assess the efficacy and safety of multiple dose levels of AZD8630 administered via a dry powder inhaler in adults with uncontrolled asthma at risk of exacerbations, receiving medium -to -high dose inhaled corticosteroid (ICS)/long-acting β2-agonist (LABA).

What is the current status of trial NCT06529419?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 537 participants. The study started on 2024-08-30. Estimated completion is 2026-02-04.

What interventions are being tested in trial NCT06529419?

The interventions under investigation include: Placebo (DRUG), AZD8630 (DRUG), Inhaler (DEVICE).

Who is sponsoring clinical trial NCT06529419?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06529419's enrollment target sits among peer trials

537 63rd of 2000 higher than 1,938 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05880004 · 537 participants · NA

    Developing a Support Application for Food Pantries (SAFPAS) to Improve Client Access to Healthy Foods & Enhance Emergency Preparedness

  • NCT03772028 · 538 participants · Phase 3

    Primary Cytoreductive Surgery With or Without Hyperthermic Intraperitoneal Chemotherapy (HIPEC)

  • NCT06538038 · 538 participants

    Prospective Non-Interventional Study Comparing Osimertinib +/- Chemotherapy for EGFR-Mutated NSCLC Patients

  • NCT05614739 · 535 participants · Phase 1

    FORAGER-1: A Study of LOXO-435 (LY3866288) in Participants With Cancer With a Change in a Gene Called FGFR3

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06529419, the US trial registry maintained by the National Library of Medicine. NCT06529419 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.