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NCT00201123

Host Response to Tuberculosis and Acquired Immune Deficiency Syndrome

Completed Phase 2 Results posted Last updated 14 December 2016
What this trial tests

Phase 2 trial testing Aerosol Interferon-Gamma in Tuberculosis in 89 participants. Completed in 1 August 2007.

Timeline
1 April 2005
Primary endpoint
1 January 2007
1 August 2007

Quick facts

Lead sponsorNYU Langone Health
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment89
Start date1 April 2005
Primary completion1 January 2007
Estimated completion1 August 2007
Sites2 locations across United States, South Africa

Drugs / interventions tested

Conditions studied

Sponsor

NYU Langone Health — full company profile →

Who can join

Adults 18 to 75, any sex, with Tuberculosis or AIDS-related Complex. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study will evaluate the lung's immune response to mycobacterium tuberculosis (Mtb) infection and will modulate that response with interferon-gamma.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Immunomodulation with recombinant interferon-gamma1b in pulmonary tuberculosis.
    Dawson R, Condos R, Tse D, Huie ML, et al · · 2009 · cited 86× · PMID 19753300 · DOI 10.1371/journal.pone.0006984
  2. Interferon therapy and its association with depressive disorders - A review.
    Lai JY, Ho JX, Kow ASF, Liang G, et al · · 2023 · cited 28× · PMID 36911685 · DOI 10.3389/fimmu.2023.1048592

Verify or expand the search:

Other recruiting trials for Tuberculosis

Currently open trials in the same condition.

Other NYU Langone Health trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00201123.

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