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NCT02917200

Safety and Efficacy Study of Different DAV132 Dose Regimens in Healthy Volunteers

Completed Phase 1 Last updated 12 September 2017
What this trial tests

Phase 1 trial testing Moxifloxacin in Healthy Subjects in 150 participants. Completed in 2 December 2016.

Timeline
11 May 2016
Primary endpoint
2 December 2016
2 December 2016

Quick facts

Lead sponsorDa Volterra
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment150
Start date11 May 2016
Primary completion2 December 2016
Estimated completion2 December 2016
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Da Volterra

Who can join

Adults 18 to 60, any sex, with Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate whether different DAV132 dose regimens are safe and effective for capturing fecal residues of moxifloxacin in healthy volunteers.

Publications & conference data

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

  1. Gut OncoMicrobiome Signatures (GOMS) as next-generation biomarkers for cancer immunotherapy.
    Thomas AM, Fidelle M, Routy B, Kroemer G, et al · · 2023 · cited 100× · PMID 37365438 · DOI 10.1038/s41571-023-00785-8
  2. Optimization of an Assay To Determine Colonization Resistance to Clostridioides difficile in Fecal Samples from Healthy Subjects and Those Treated with Antibiotics.
    Harris HC, Best EL, Normington C, Saint-Lu N, et al · · 2020 · cited 5× · PMID 33139292 · DOI 10.1128/aac.01401-20

Verify or expand the search:

Other trials of Moxifloxacin

Trials testing the same drug.

Other recruiting trials for Healthy Subjects

Currently open trials in the same condition.

Other Da Volterra trials

Trials by the same sponsor.

Verify against primary sources

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/NCT02917200.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing