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NCT Number: NCT03055247

Combination of Ibuprofen, G-CSF and Plerixafor as Stem Cells Mobilization Regimen in Patients Affected by X-CGD

This is a phase II exploratory study conducted to evaluate the safety and efficacy of the combination of Ibuprofen, G-CSF and Plerixafor as stem cell mobilization regimen in patients affected by X-CGD.

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Key information

About this study

We designed a mobilization trial with the aim of collecting a sufficient number of HSPC in X-CGD patients; it is well known that this procedure is challenging for these patients, potentially due to functional defects induced by their chronic inflammatory state.

The combination of G-CSF and Plerixafor is considered state of the art for HSPC harvest in gene therapy trials; we considered to add a non-steroidal inflammatory drug to increase HSPC mobilization and reduce inflammation that could have a role in altering HSPC content.

If this trial confirms the synergistic effect of the three drugs under investigation, such a regimen will be considered for a HSPC mobilization in future gene therapy trial for X-CGD patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Genetic diagnosis of X-CGD
  • 18-45 years of age
  • Karnofsky Index > 80 %
  • Adequate cardiac, renal, hepatic and pulmonary function.
  • Negative thrombophilic screen and negative history for previous thrombotic events
  • Written informed consent

Exclusion criteria

  • Previous Bone Marrow Transplantation or previous Gene Therapy.
  • Use of other investigational agents within 4 weeks prior to study enrolment (within 6 weeks if use of long-acting agents).
  • Ongoing IFN-γ treatment (within 4 weeks).
  • Symptomatic inflammatory bowel disease.
  • Symptomatic viral, bacterial, or fungal infection within 6 weeks of eligibility
  • Neoplasia (except local skin cancer) or history of "familial" cancer
  • Myelodysplasia or other serious hematological disorder
  • History of uncontrolled seizures and deep venous thrombosis
  • Other systemic disease judged as incompatible with the procedure
  • Positivity for HIV and/or HCV RNA and/or HbsAg and/or HBV DNA
  • Active alcohol or substance abuse within 6 months of the study.
  • Contraindications to IBU, G-CSF, Plerixafor or Pantoprazole administration

Treatment and study plan

Ibuprofen

Drug

Ibuprofen: 3 mg/kg tid (total daily dose: 9 mg/kg); administered orally from day 1 to day 5 and then from day 14 to the day before the last LP.

Myelostim

Drug

Myelostim (G-CSF): 5 µg/kg bid (total daily dose 10 µg/kg); administered subcutaneously from day 19 to the day of the last LP.

Mozobil

Drug

Mozobil (Plerixafor): 0,24 mg/kg daily. When CD34+ are ≥ 10 /μL Plerixafor will be administered subcutaneously from the next day (or from day 24 if CD34+ are < 10 /μL) to the day of the last LP.

Primary outcomes

  1. Percentage of patients experiencing adverse events

    Time frame: up to 30 days after the last LP

    Percentage of patients experiencing adverse events, as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse events (CTCAe v3.0, 2006) (all grades).

  2. Number of CD34+ collected per body weight after the last LP

    Time frame: Day 21-24

    Cytofluorimetric analysis for CD34 on PB and on collected PBSC to calculate the number of CD34+ cells collected per kg body weight. The analysis will be performed at the end of the LP(s) (Day 21-24)

Secondary outcomes

  1. Change in number of CD34+ cells in PB before and after administration of Ibuprofen

    Time frame: Day 6 and day 7

    Cytofluorimetric analysis to determine the number of CD34+ cells present in PB on day 6 and 7 compared to before the administration of Ibuprofen

  2. Transduction efficiency

    Time frame: Through study completion, an average of 1 year

    Efficient transduction of mobilized HSPC with a lentiviral vector encoding for a corrective cDNA of the human gp91phox gene. Frequency and Vector Copy Number tested by PCR.

  3. DHR (dihydrorhodamine) test in myeloid progeny

    Time frame: Through study completion, an average of 1 year

    Correction of the functional defects in the differentiated myeloid progeny

  4. Functional characterization of mobilized CD34+ cells.

    Time frame: Through study completion, an average of 1 year

    Phenotype analysis (FACS).

  5. Functional characterization of mobilized CD34+ cells.

    Time frame: Through study completion, an average of 1 year

    Clonogenic activity (CFU-C) before and after transduction.

  6. Functional characterization of mobilized CD34+ cells.

    Time frame: Through study completion, an average of 1 year

    Repopulating activity of mobilized CD34+ cells in immunodeficient mice.

Study contacts

Contact information is provided by the study sponsor or research team.

Alessandro Aiuti, MD, PhD

CONTACT

[email protected]

+390226434875

Fabio Ciceri, MD, PhD

CONTACT

[email protected]

39 02.2643.3903

Sponsors and collaborators

Lead sponsor

IRCCS San Raffaele

Other

Collaborators

  • Fondazione Telethon

Registry information

Official study title

A Multicentric, Exploratory, Non-randomised, Non-controlled, Prospective, Open-label Phase II Study Evaluating Safety and Efficacy of IBU, G-CSF and Plerixafor as Stem Cell Mobilization Regimen in Patients Affected by X-CGD

Acronym: XCGD-MOBI

Important dates

Study start
2015
Primary completion
2023
Study completion
2026
First posted
Feb 16, 2017
Registry last updated
Sep 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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