A Safety and Tolerability Study OF PUR118 In Subjects With Cystic Fibrosis

NCT01543191 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2013-07-19

No results posted yet for this study

Summary

The purpose of this study is to determine whether PUR118 is safe and tolerable in a population of subjects with Cystic Fibrosis.

Conditions

Interventions

DRUG

PUR118

low dose and high dose for 3 doses, BID

Sponsors & Collaborators

  • Celerion

    collaborator INDUSTRY
  • Pulmatrix Inc.

    lead INDUSTRY

Principal Investigators

  • Stephen Smith, MD · Celerion

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01543191 on ClinicalTrials.gov