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Doxycycline for Emphysema in People Living With HIV (The DEPTH Trial)

About

Brief Summary

The purpose of this study is to determine if doxycycline will reduce progression of emphysema in people living with HIV.

The secondary objectives are to examine the effects of doxycycline on change in quantity of emphysema, six minute walk distance, patient reported outcomes, ratio of forced expiratory volume in 1 second and forced vital capacity. Secondary objectives will also describe the safety and tolerability of doxycycline and determine if doxycycline is associated with development of antibiotic-resistant bacterial infections.

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase 2

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
30 Years
Maximum Age
N/A

Inclusion Criteria:

  • Male or female age 30 years and older at screening visit.
  • HIV-1 infection, documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to the enrollment visit, and confirmed by a licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 antigen, plasma HIV-1 RNA viral load.
  • Current or former smoker with at least a 3 pack-year history of cigarette smoking at screening visit.
  • Evidence of emphysema on high resolution CT (HRCT) of the chest done at pre-entry visit. Emphysema is defined as 5 to 35% of voxels with density < -950 Hounsfield Units (HU).
  • Low DLCO, defined as average of screening and pre-entry measurements < LLN (lower bound of the 95% confidence interval for the normal predicted value) of the Global Lung Initiative (GLI) predicted set for DLCO adjusted for barometric pressure. Screening and pre-entry measurements must be within 10% of each other.
  • HIV-1 RNA level < 200 copies/ml within 90 days prior to the Entry/Baseline visit by any US laboratory that has a Clinical Laboratory Improvement Amendments (CLIA) certification or its equivalent.
  • CD4 cell count > 200 cells/mm3 within 90 days prior to the Entry/Baseline visit.by any US laboratory that has a CLIA certification or its equivalent.
  • Stable antiretroviral therapy for greater than or equal to 8 weeks prior to the Entry/Baseline visit. Substitutions of one formulation of a drug for another are not considered changes in antiretroviral therapy for the purpose of defining stable therapy.
  • Calculated creatinine clearance (CrCl) greater than or equal to 60 mL/min as estimated by the Cockcroft-Gault equation within 45 days prior to the Entry/Baseline visit.
  • Serum ALT and AST < 3 x upper limit of normal within 45 days prior to the Entry/Baseline visit.
  • Participants on therapy for COPD must be on stable therapy for at least 4 weeks prior to the Entry/Baseline visit.
  • Documentation of serum alpha-1-antitrypsin level above the lower limit of normal from a test done at any time prior to the Entry/Baseline visit.
  • Provision of signed and dated written informed consent.
  • Stated willingness to adhere to all study procedures and anticipated availability for the duration of the study.
  • Life expectancy > 2 years in the opinion of the site investigator.
  • Ability to take oral medication and willingness to adhere to the study drug.
  • For individuals of reproductive potential, negative serum or urine pregnancy test with a sensitivity of less than or equal to 25 mIU/mL at the screening visit. This will be repeated at the Entry/Baseline visit.

Exclusion Criteria:

  • Pulmonary infection, acute COPD exacerbation, acute opportunistic infection within 30 days prior to the Entry/Baseline visit.
  • Any acute or serious illness requiring systemic treatment and/or hospitalization within 30 days prior to the Entry/Baseline visit.
  • Decompensated cirrhosis defined as an acute deterioration in liver function in a patient with cirrhosis and is characterized by jaundice, ascites, hepatic encephalopathy, hepatorenal syndrome or variceal hemorrhage.
  • History of, or planned, wedge resection, lobectomy, pneumonectomy, or lung volume reduction surgery.
  • History of, or planned, endobronchial valve placement for lung volume reduction.
  • Significant parenchymal lung disease other than emphysema or chronic bronchitis (e.g. sarcoidosis, MAI infection, pulmonary fibrosis, lung cancer).
  • Previous allergy or intolerance to doxycycline or other drugs in the tetracycline class (e.g. minocycline, tetracycline).
  • Breastfeeding individuals.
  • Receipt of any investigational* drug within 30 days prior to the Entry/Baseline visit. Note: for the purpose of this protocol, investigational drug refers to a drug that is not FDA approved for any indication. COVID vaccines available under emergency use authorization are allowed.
  • Need for concomitant use of barbiturates; carbamazepine; phenytoin
  • Use of systemic retinoids (eg. Isotretinoin [Accutane]) or Vitamin A within 30 days prior to the Entry/Baseline visit. Note: Multivitamin containing Vitamin A use is permitted.
  • Use of any systemic antibiotic (e.g., doxycycline or other tetracycline, azithromycin) within 7 days prior to the Entry/Baseline visit.
  • Any condition including active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
  • History of recurrent C. difficile infection or C. difficile infection within 30 days prior to the Entry/Baseline visit.
  • History of Pneumocystis pneumonia.
  • Inability to stop supplemental oxygen for 15 minutes to perform a DLCO maneuver.
  • Has changes to the chest that preclude adequate HRCT imaging (e.g. Metallic objects in the chest such as shrapnel or pacemaker leads)

Join this Trial

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Study Stats
Protocol No.
22-000897
Category
Pulmonary Disease
Contact
Maria Granone
Location
  • UCLA Westwood
For Providers
NCT No.
NCT05382208
For detailed technical eligibility, visit ClinicalTrials.gov.