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Completed Phase 1 Interventional Results available

Safety and Pharmacokinetic Study of N6022 in Subjects With Cystic Fibrosis Homozygous for the F508del-CFTR Mutation

ClinicalTrials.gov ID: NCT01746784

Public ClinicalTrials.gov record NCT01746784. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 7:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study of N6022 to Evaluate Safety and Pharmacokinetics in Subjects With Cystic Fibrosis Homozygous for the F508del-CFTR Mutation (SNO1)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of N6022, and to obtain descriptive information on the effect of N6022 on biomarkers of CFTR function and inflammation in adult cystic fibrosis subjects who are homozygous for the F508del-CFTR mutation.

Study identification

NCT ID
NCT01746784
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Nivalis Therapeutics, Inc.
Industry
Enrollment
66 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2014 (Type not available)
Primary completion
Apr 2014 (Actual)
Completion
May 2014 (Actual)
Last update posted
Nov 24, 2014

2014

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
Providence Alaska Medical Center Anchorage Alaska 99508 —
Stanford University Palo Alto California 94304 —
Children's Hospital Colorado Aurora Colorado 80045 —
National Jewish Health Denver Colorado 80206 —
Northwestern University Chicago Illinois 60611 —
University of Iowa Children's Hospital Iowa City Iowa 52242 —
Johns Hopkins Hospital Baltimore Maryland 21287 —
Boston Children's Hospital Boston Massachusetts 02115 —
University of Minnesota Minneapolis Minnesota 55455 —
Washington University St Louis Missouri 63110 —
University of North Carolina Chapel Hill North Carolina 27599 —
Cincinnati Children's Hospital Cincinnati Ohio 45229 —
Rainbow Babies and Children's Hospital - Case Medical Center Cleveland Ohio 44106 —
Nationwide Children's Hospital Columbus Ohio 43205 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania 15224 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01746784, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 24, 2014 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01746784 live on ClinicalTrials.gov.

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