ConductScience.org, home

Trial · NCT02739477

Tolerance and Activity Evaluation of High Doses of Favipiravir Against Ebola Virus in the Semen

NCT02739477, Phase 2, Terminated, Institut National de la Santé Et de la Recherche Médicale, France

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Tolerance and Activity Evaluation of High Doses of Favipiravir Against Ebola Virus in the Semen. Trials, record NCT02739477. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02739477

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Tolerance and Activity Evaluation of High Doses of Favipiravir Against Ebola Virus in the Semen
NCT number
NCT02739477
Status
Terminated
Phases
Phase 2
Enrollment
2 participants, actual
Lead sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Conditions
Ebola Virus Survivor
Interventions
Favipiravir
First posted
2016-04-15
Last updated
2025-02-24

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of patients undergoing grade 3 or 4 clinical or biological adverse events related to Favipiravir (Common Terminology Criteria for Adverse Events, CTCAE, v4.03)Day 14Day 1 is the first day of favipiravir intake
SecondaryEvolution of EBOV semen RNA and infectious loadsSemen collection will be performed at least at Day 7, Day 14, Day 21 and Day 90From Day 14 to Day 90, semen EBOV PCR will be performed every 3 weeks until their semen tests negative for virus twice by RT-PCR, with an interval of one week between tests.
SecondaryPlasma and semen trough concentrations of favipiravirPlasma collection at Day 3, Day7, Day 10 and Day 14. Semen collection at Day 7 and Day 14
SecondaryGenetic variations associated with favipiravir expositionBlood collection at Day 1 will be used for further genotyping.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
35127447RESULT

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02739477

GET https://conductscience.org/api/trials/v1/NCT02739477/registered