ADENOCLEAR: Treatment of Adenovirus Disseminated Infections in Hematopoietic Stem Cell Transplant Patients With Adenovirus Digestive Replication

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT03481244
Collaborator
(none)
400
44

Study Details

Study Description

Brief Summary

Disseminated Adv infections are associated with high morbidity and mortality in HSCT pediatric patients. The most common source of Adv infection after pediatric HSCT is the host digestive tract where latent Adv are reactivated after engraftment. We have shown in a monocentric study that Adv viral load in stools is a predictive factor of blood infection in children with digestive Adv infections. We assume that an early treatment, with antiviral drugs, such as cidofovir and brincidofovir, may avoid severe Adv infections and diseases and thus that molecular surveillance in stool is a critical factor for the control of Adv reactivations.

The study has two main objectives: (i) confirming the impact of Adv viral load in stools on the occurrence of blood infection based on a multicentric prospective cohort study design; and (ii) determining the prognostic and predictive factors for efficacy and toxicity of antiviral drugs, such as brincidofovir and cidofovir.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    400 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Treatment of Adenovirus Disseminated Infections in Hematopoietic Stem Cell Transplant Patients With Adenovirus Digestive Replication- A Pharmaco-epidemiological Prospective Study
    Anticipated Study Start Date :
    Apr 1, 2020
    Anticipated Primary Completion Date :
    Mar 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. rate of Adv blood infection according to levels of Adv DNA in stool samples. [100 days]

      Adv blood infection is defined as plasma Adv DNA level greater than 200 copies per milliliter

    2. rate of response to antiviral drugs [100 days]

      Success will be defined as undetectable level of DNA of Adv in blood after a maximum of 4 weeks of treatment. After 4 weeks of treatment any detectable level of Adv DNA will be considered as a failure.

    Secondary Outcome Measures

    1. Adv DNA levels > 5 log10 copies/ml in stool [100 days]

      measured at the end of treatment

    2. Time required achieving 50% decrease of Adv load and undetectable Adv DNA. [100 days]

    3. Time required achieving 90% decrease of Adv load and undetectable Adv DNA. [100 days]

    4. Incidence of Adv probable or proven disease [100 days]

      We will use the definitions recommended by ECIL (detailed in Appendix 1). Digestive infection: positive Adv PCR in stool Local infection: positive Adv PCR in biopsy material or body fluids other than peripheral blood. Systemic infection/viremia: positive Adv PCR in peripheral blood. Probable disease: Adv infection plus corresponding symptoms and signs without histological confirmation. Proven disease: Adv infection plus corresponding symptoms related to the infection and histological confirmation of Adv in the appropriate location.

    5. Incidence of diarrhea [100 days]

    6. Incidence of acute digestive graft versus host disease (aGvHD) [100 days]

    7. Overall survival. [100 days]

    8. Incidence of Adv probable or proven disease [100 days]

    9. Genotypic analysis of the Adv DNA polymerase [100 days]

    10. Detection and quantification of herpesviruses in blood [100 days]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    2 Months to 20 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Allogeneic hematopoietic stem cell transplantation from any donor other than full-matched related donor

    • Age above 2 months and under 20 years

    • Provide written informed consent from the parents (if <18) and child

    • Free, informed and written consent, signed by the patient and investigator before any Study examination. If the patient is a minor by child (if possible) and both parents or child and the legal representative in case only one parent is alive

    Exclusion Criteria:
    • Hematopoietic stem cell transplantation from full-matched related donor

    • Females who are pregnant or currently nursing

    • Any patient receiving cidofovir, ribavirin or any other anti-viral drug under development given in order to treat or prevent

    • Current disease attributed to adenovirus infection

    • Lack of affiliation to a social security scheme (as a beneficiary or assignee).Current disease attributed to adenovirus infection

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Assistance Publique - Hôpitaux de Paris

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Assistance Publique - Hôpitaux de Paris
    ClinicalTrials.gov Identifier:
    NCT03481244
    Other Study ID Numbers:
    • K140902J
    First Posted:
    Mar 29, 2018
    Last Update Posted:
    Feb 10, 2020
    Last Verified:
    Feb 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 10, 2020