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Clinical Trials/NCT03488394
NCT03488394
Active, not recruiting
Phase 1

Phase I/II Study Evaluating Safety and Efficacy of Autologous Hematopoietic Stem and Progenitor Cells Genetically Modified With IDUA Lentiviral Vector Encoding for the Human α-L-iduronidase Gene for the Treatment of Patients Affected by Mucopolysaccharidosis Type I, Hurler Variant

Orchard Therapeutics1 site in 1 country8 target enrollmentMay 11, 2018

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Mucopolysaccharidosis IH
Sponsor
Orchard Therapeutics
Enrollment
8
Locations
1
Primary Endpoint
Overall survival
Status
Active, not recruiting
Last Updated
4 months ago

Overview

Brief Summary

This is a phase I/II study evaluating safety and efficacy of autologous hematopoietic stem and progenitor cells genetically modified with IDUA lentiviral vector encoding for the human α-L-iduronidase gene for the treatment of patients affected by Mucopolysaccharidosis Type I, Hurler variant

Detailed Description

Pediatric patients with mucopolysaccharidosis type I will be treated with genetically modified autologous hematopoietic stem cells collected from mobilized peripheral blood (or bone marrow if mobilization is not feasible) and transduced with IDUA lentiviral vector encoding for the human α-L-iduronidase gene. Patients will be followed for 8 years after gene therapy. After completing participation in this study, subjects will be offered enrollment into an approved long term follow-up (LTFU) study which will enable continued follow-up for up to 15 years post-treatment (per regulatory guidelines for follow up of patients treated with ATMPs).

Registry
clinicaltrials.gov
Start Date
May 11, 2018
End Date
March 1, 2028
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Written informed consent by parent/legal guardian
  • Sex: Males and Females
  • Age: ≥ 28 days and ≤ 11 years old
  • Biochemically and molecularly proven MPS IH
  • Lansky index \>80%
  • Indication to hematopoietic stem cell transplant
  • Lack of a non-heterozygous (for mutated IDUA) HLA-matched sibling donor or a ≥7/8 (4 digits high-resolution typing) HLA-matched cord blood donor with a cellularity ≥5 x 10\^7 Total Nucleated Cells (TNC)/Kg after 1-month search.(This criterion will not apply to patients whose country of origin does not offer unrelated donor cord blood transplantation).
  • Adequate cardiac, renal, hepatic and pulmonary functions

Exclusion Criteria

  • Use of other investigational agents within 4 weeks prior to study enrolment (within 6 weeks if use of long-acting agents)
  • Severe, active viral, bacterial or fungal infection at eligibility evaluation
  • Patients affected by neoplasia or family history of familial cancer syndromes
  • Cytogenetic alterations associated with high risk of developing hematological malignancies
  • History of uncontrolled seizures
  • Patients with end-organ damage or any other severe disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study
  • Positivity for HIV (serology or RNA), and/or HbsAg and/or HBV DNA and/or HCV RNA and/or Treponema Pallidum or Mycoplasma active infection
  • Patients with DQ/IQ \<70
  • Previous allogeneic hematopoietic stem cells transplantation or gene therapy with a different product
  • Contraindications to PeIMP (G-CSF, Plerixafor, Busulfan, Fludarabine, Rituximab)

Outcomes

Primary Outcomes

Overall survival

Time Frame: 8 years

Number and percentage of subjects alive at the end of the trial

Achievement of haematological engraftment

Time Frame: within day +45 after gene therapy

Percentage of subjects with both neutrophil count more than 500/mm3 and platelets more than 20,000/mm3 (in the absence of platelet transfusion for seven consecutive days) on 3 consecutive blood counts in the first 45 days from ATIMP injection.

Safety of the administration of autologous haematopoietic stem cells transduced with IDUA LV - Short term tolerability

Time Frame: 0-24 hours from ATIMP injection

Percentage of subjects not experiencing short-term adverse events of any grade and systemic reactions

Overall safety and tolerability (AE)

Time Frame: Assessed at multiple timepoints up to 8 years post-treatment

The number of AEs (expected/unexpected and/or related/not related) and SAEs (expected/unexpected and/or related/not related) and the percentage of subjects experiencing AEs (expected/unexpected and/or related/not related) and SAEs (expected/unexpected and/or related/not related) will be summarized by severity and within body system involved. Narratives will also be presented. The rate of occurrence of these events will also be estimated.

IDUA activity in blood (up to supraphysiologic levels) at 1-year post-treatment

Time Frame: Assessed at multiple timepoints up to 8 years post-treatment

IDUA activity measured on peripheral blood dried spot

Safety of the administration of autologous haematopoietic stem cells transduced with IDUA LV - Absence of Replication Competent Lentivirus

Time Frame: Assessed at multiple timepoints up to 8 years post-treatment

Percentage of subjects without Replication Competent Lentivirus

Safety of the administration of autologous haematopoietic stem cells transduced with IDUA LV - Absence of malignancy or abnormal clonal proliferation

Time Frame: Assessed at multiple timepoints up to 8 years post-treatment

Percentage of subjects without abnormal clonal proliferation

Secondary Outcomes

  • Anti-IDUA antibody immune response(Assessed at multiple timepoints up to 8 years post-treatment)
  • Achievement of supraphysiologic IDUA activity in blood(Assessed at multiple timepoints up to 8 years post-treatment)
  • Growth velocity(Assessed at multiple timepoints up to 8 years post-treatment)
  • IDUA activity in plasma(Assessed at multiple timepoints up to 8 years post-treatment)
  • Engraftment of transduced cells ≥ 0.30 VCN/genome(Assessed at multiple timepoints up to 8 years post-treatment)
  • Normalization of urinary GAGs(Assessed at multiple timepoints up to 8 years post-treatment)
  • Normalization of spleen and liver(Assessed at multiple timepoints up to 8 years post-treatment)

Study Sites (1)

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