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N/A N=31 Randomized Treatment

Improving Treatment of Nontuberculous Mycobacterial Infection in Cystic Fibrosis

Cystic Fibrosis

Enrolled (actual)
31
Serious AEs
0.0%
Results posted
Feb 2021
Primary outcome: Primary: Median Maximal Drug Concentration (Cmax) — 16.56; 12.5; 11.2; 3.0 mg/L

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Ethambutol (Drug); Rifampin (Drug); Azithromycin (Drug); Pancrelipase (Drug)
Age
Pediatric, Adult · 16+ yrs
Sex
All
Sponsor
University of Colorado, Denver
Primary completion
Jun 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Median Maximal Drug Concentration (Cmax)
16.56; 12.5; 11.2; 3.0; 4.2; 4.3
SECONDARY
Other PK Measures: Median Time to Maximal Drug Concentration (Tmax)
1.5; 1.5; 2.5; 2.3; 2.3; 2.0
SECONDARY
Other PK Measures: Half-life (t1/2)
3.8; 3.4; 3.4; 5.3; 4.3; 4.7
SECONDARY
Other PK Measures: Drug Clearance
5.1; 7.9; 7.6; 45.3; 42.4; 37.3
SECONDARY
Other PK Measures: Volume of Distribution (Vd)
31.3; 39.7; 37.4; 352.8; 274.6; 354.3
SECONDARY
Covariates of PK Measures: C-reactive Protein (CRP)
0.2; 0.8
SECONDARY
Covariates of PK Measures: Circulating Neutrophil Count
3.0; 3.8
SECONDARY
Covariates of PK Measures: Body Mass Index
23.0; 21.9
SECONDARY
Covariates of PK Measures: Creatinine
1.0; 0.9
SECONDARY
Area Under the Curve (AUC)
118.3; 76; 79.2; 21.4; 21.8; 23.6

Summary

The purpose of this study is to determine antimycobacterial drug pharmacokinetics (PK) and pharmacodynamics (PD) in patients with cystic fibrosis (CF) to improve treatment of nontuberculous mycobacterial (NTM) lung disease.

Eligibility Criteria

CF Subject Inclusion Criteria:

  • CF diagnosis defined as a sweat chloride >60mEq/L and/or the presence of two disease-causing CFTR mutations.
  • Ages 16 years and above.
  • Pancreatic insufficient status defined as previous fecal pancreatic elastase 40% predicted.
  • Willing to participate in and comply with the study procedures, and willingness of a parent or legally authorized representative to provide written informed consent for those subjects less than 18 years of age.

Healthy Control Inclusion Criteria:

  • Ages 18 years and above.
  • BMI below 30 to best match CF body type.
  • Willing to participate in and comply with the study procedures, and willingness of a parent or legally authorized representative to provide written informed consent for those subjects less than 18 years of age.

CF Subject Exclusion Criteria:

  • Allergy or intolerance to rifampin, ethambutol, or azithromycin.
  • Hepatic insufficiency defined as having an AST or ALT greater than three times the upper limit of normal at the screening appointment.
  • Previous surgical bowel resection.
  • Previous lung transplant.
  • Use of medications known to interact with the antimycobacterial drug levels; of note, the most common interactions in CF patients are the use of itraconazole, voriconazole, and ivacaftor. We will have subjects hold H2 blockers and proton pump inhibitors for 3 days prior to each PK study day.
  • Inability to hold azithromycin: Subjects will not be excluded if they are on chronic azithromycin for immunomodulatory purposes; however, we will ask that the subjects hold the azithromycin starting at the screening visit, through a 2 week wash-out period prior to Visit 2, and remain off through the end of Visit 3 (about 4 weeks total).
  • Acute exacerbations: exclusion if any addition of oral, IV, or inhaled antibiotics, or an acute gastrointestinal illness with vomiting or diarrhea in the 2 weeks prior to each visit. No exclusion for previously prescribed alternating chronic inhaled or oral antibiotics.
  • We will also exclude pregnant women (urine pregnancy test will be performed for females on the day of each PK study) and decisionally challenged subjects.

Healthy Control Exclusion Criteria:

  • Allergy or intolerance to rifampin, ethambutol, or azithromycin.
  • Hepatic insufficiency defined as having an AST or ALT greater than three times the upper limit of normal at the screening appointment.
  • Previous chronic GI disease or surgical bowel resection.
  • Use of medications known to interact with the antimycobacterial drug levels. We will have subjects hold H2 blockers and proton pump inhibitors for 3 days prior to the PK study day.
  • Acute illness: exclusion if respiratory illness requiring antibiotics or gastrointestinal illness with vomiting or diarrhea in the 2 weeks prior to the PK visit.
  • We will also exclude pregnant women (urine pregnancy test will be performed on the day of PK study) and decisionally challenged subjects.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02372383). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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