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

NCT02124278 · ClinicalTrials.gov registry record · Phase 1

Safety and Tolerability of Single Ascending Doses of PUL-042 Inhalation Solution in Healthy Subjects

A Phase 1 study, sponsored by Pulmotect.

Completed
Registry status
Phase 1
Development phase
42
Enrollment target

NCT02124278: Completed Phase 1 study, sponsored by Pulmotect.

NCT02124278 is a Phase 1 study that has completed, run by Pulmotect. The registered enrollment target is 42 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02124278, a Phase 1 study, has completed, sponsored by Pulmotect.

COMPLETED
Registry status
Phase 1
Development phase
42 participants
Enrollment target

Study Summary

The purpose is to determine if single doses of PUL-042 inhalation solution are safe in healthy subjects.

Interventions

  • DRUG PUL-042 Inhalation Solution

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2014-02
Est. Completion 2014-10
Phase Phase 1
Pulmotect

5 total trials

What the finished NCT02124278 record still lists

NCT02124278 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower).

The record links to 0 conditions, and to 1 intervention - of which PUL-042 Inhalation Solution is the first listed.

NCT02124278 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02124278 about?

NCT02124278 is a clinical study titled "Safety and Tolerability of Single Ascending Doses of PUL-042 Inhalation Solution in Healthy Subjects". The purpose is to determine if single doses of PUL-042 inhalation solution are safe in healthy subjects.

What is the current status of trial NCT02124278?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2014-02. Estimated completion is 2014-10.

What interventions are being tested in trial NCT02124278?

The interventions under investigation include: PUL-042 Inhalation Solution (DRUG).

Who is sponsoring clinical trial NCT02124278?

This trial is sponsored by Pulmotect, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02124278's enrollment target sits among peer trials

42 1105th of 2000 higher than 876 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

  • NCT02852213 · 42 participants · Phase 1

    A Single-Stage, Adaptive, Open-label, Dose Escalation Safety and Efficacy Study of AADC Deficiency in Pediatric Patients

  • NCT03136146 · 42 participants · Phase 2

    Combination Chemotherapy in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma, Burkitt Lymphoma/Leukemia, or Double-Hit Lymphoma/Leukemia

  • NCT03178149 · 42 participants · Phase 1

    A Study of the Safety and Tolerability of ASP7317 in Senior Adults Who Are Losing Their Clear, Sharp Central Vision Due to Geographic Atrophy Secondary to Dry Age-related Macular Degeneration

  • NCT03663530 · 42 participants · NA

    Circadian Misalignment and Energy Balance

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02124278, the US trial registry maintained by the National Library of Medicine. NCT02124278 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.