Purpose

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.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Confirmed clinical diagnosis of Cystic Fibrosis (CF) who are homozygous for the F508del CF transmembrane conductance regulator (CFTR) mutation - Stable pulmonary status - Lung function >= 40 and <= 90% of predicted normal for age, gender and height at Screening

Exclusion Criteria

  • History of solid organ or hematopoietic transplant - Cirrhosis with portal hypertension - Use of CFTR modulator therapy within 60 days prior to Screening

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Part 1: ABBV-3067 + Placebo
Participants will receive various dosing regimens for ABBV-3067 plus placebo ABBV-2222 taken orally depending on arm assignment.
  • Drug: ABBV-3067
    Tablet or capsule taken orally
  • Drug: Placebo ABBV-2222
    Capsule taken orally
Experimental
Part 1: ABBV-3067 + ABBV-2222
Participants will receive fixed dose of ABBV-3067 plus various dosing regimens for ABBV-2222 taken orally depending on arm assignment.
  • Drug: ABBV-3067
    Tablet or capsule taken orally
  • Drug: ABBV-2222
    Capsule taken orally
Placebo Comparator
Part 1 and Part 2: Placebo
Participants in Part 1 and Part 2 will receive placebo ABBV-3067 plus placebo ABBV-2222 taken orally.
  • Drug: Placebo ABBV-3067
    Tablet or capsule taken orally
  • Drug: Placebo ABBV-2222
    Capsule taken orally
Experimental
Part 2: ABBV-3067 + ABBV-2222
Participants will receive various dosing regimens for ABBV-3067 plus a fixed dose of ABBV-2222 taken orally depending on arm assignment.
  • Drug: ABBV-3067
    Tablet or capsule taken orally
  • Drug: ABBV-2222
    Capsule taken orally

Recruiting Locations

Vanderbilt University Medical Center /ID# 212353
Nashville, Tennessee 37232

More Details

Status
Recruiting
Sponsor
AbbVie

Study Contact

ABBVIE CALL CENTER
844-663-3742
abbvieclinicaltrials@abbvie.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.