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Completed Phase 2 Interventional Results available

A Phase 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222

ClinicalTrials.gov ID: NCT03969888

Public ClinicalTrials.gov record NCT03969888. 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 Sep 10, 2026, 2:21 PM 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 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222 in Cystic Fibrosis Subjects Who Are Homozygous for the F508del Mutation

Brief summary

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

This study will evaluate the safety, tolerability, and efficacy of ABBV-3067 given alone and in combination with various doses of ABBV-2222 in adults with Cystic Fibrosis who are homozygous for the F508del mutation.

Study identification

NCT ID
NCT03969888
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
78 participants

Conditions and interventions

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
Dec 10, 2019
Primary completion
Jun 8, 2022
Completion
Jun 8, 2022
Last update posted
Jun 27, 2023

2019 – 2022

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
University of Arkansas /ID# 212541 Little Rock Arkansas 72205
Tampa General Hospital /ID# 212342 Tampa Florida 33606
University of Iowa Hospitals and Clinics /ID# 212351 Iowa City Iowa 52242
Univ Michigan Med Ctr /ID# 212657 Ann Arbor Michigan 48109
Cardinal Glennon Children's Hospital /ID# 212349 St Louis Missouri 63104
Washington University-School of Medicine /ID# 212352 St Louis Missouri 63110
Nationwide Children's Hospital /ID# 213158 Columbus Ohio 43205-2664
Medical University of South Carolina /ID# 212187 Charleston South Carolina 29425
Vanderbilt University Medical Center /ID# 212353 Nashville Tennessee 37232
University of Utah /ID# 212350 Salt Lake City Utah 84112-5500

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03969888, 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 Jun 27, 2023 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03969888 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →