deltatrials
Terminated PHASE1 INTERVENTIONAL 2-arm NCT03309358

A Study of the Safety and Tolerability of Inhaled SNSP113 in Healthy Subjects and Subjects With Stable Cystic Fibrosis

A Multiple-Site, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose (SAD) Study to Assess the Safety and Tolerability of Inhaled SNSP113 in Healthy Male Subjects (Part A) and Subjects With Stable Cystic Fibrosis (Part B)

Sponsor: Synspira, Inc.

Updated 5 times since 2017 Last updated: May 23, 2018 Started: Sep 28, 2017 Primary completion: Dec 18, 2017 Completion: Dec 18, 2017
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Successful completion of Part A. Company decision to end early.

A PHASE1 clinical study on Antibiotic Resistant Infection and Burkholderia Cepacia Infection, this trial is terminated or withdrawn. The trial is conducted by Synspira, Inc. and has accumulated 5 data snapshots since 2017. Infectious disease trials contribute critical data for public health response and treatment development.

Status Flow

~Oct 2017 – ~Jun 2018 · 8 months · monthly snapshotRecruiting~Jun 2018 – ~Jan 2021 · 31 months · monthly snapshotTerminated~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotTerminated~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotTerminated~Sep 2024 – present · 22 months · monthly snapshotTerminated

Change History

5 versions recorded
  1. Sep 2024 — Present [monthly]

    Terminated PHASE1

  2. Jul 2024 — Sep 2024 [monthly]

    Terminated PHASE1

  3. Jan 2021 — Jul 2024 [monthly]

    Terminated PHASE1

  4. Jun 2018 — Jan 2021 [monthly]

    Terminated PHASE1

    Status: RecruitingTerminated

  5. Oct 2017 — Jun 2018 [monthly]

    Recruiting PHASE1

    First recorded

Sep 2017

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Synspira, Inc.
Data source: Synspira, Inc.

For direct contact, visit the study record on ClinicalTrials.gov .