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RecruitingPhase 1

ISP-001: Sleeping Beauty Transposon-Engineered B Cells for MPS I

Immusoft of CA, Inc. · NCT05682144

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 10+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 1
Target enrollment
11
US sites recruiting
2
Study start
April 12, 2023
Record last updated
July 17, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

A first-in-human study using ISP-001 in patients with Mucopolysaccharidosis Type I Hurler-Scheie and Scheie.

Being studied: Autologous Plasmablasts (B cells)

Conditions: Mucopolysaccharidosis IH/S; Mucopolysaccharidosis IS

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Diagnosis of Mucopolysaccharidosis type I Hurler-Scheie or Scheie syndrome.
  • Age ≥ 10 years at time of study registration.
  • Creatinine clearance, calculated or measured directly, that is >60ml/min/1.73m2.
  • Ejection fraction ≥ 40% by echocardiogram.
  • Must commit to traveling to the study site for the necessary follow-up evaluations.
  • Must agree to stay \<45-minute drive from the study site for a minimum of 5 days after cell infusion.

Exclusion Criteria

  • Known familial inherited cancer syndrome. Suspected cases will be investigated, per the physicians discretion, using relevant genetic tests to determine presence of germline mutations.
  • History of B cell related cancer, EBV lymphoproliferative disease or autoimmune disorders.
  • Evidence of active graft-vs-host disease.
  • Underwent a previous hematopoietic stem cell transplant (HSCT).
  • Requirement for systemic immune suppression.
  • Requirement for continuous supplemental oxygen.
  • Any medical condition likely to interfere with assessment of safety or efficacy of the study treatment.
  • In the investigator's judgement, the subject is unlikely to complete all protocol-required study visits or procedures, including follow up visits, or comply with the study requirements for participation.

Other protocol defined inclusion/exclusion criteria may apply.

Recruiting US locations

  • UCSF Benioff Children's Hospital Oakland

    Oakland, CA 94609

    Site contact: Daniel Schrader · Daniel.Schrader@ucsf.edu

  • University of Minnesota

    Minneapolis, MN 55455

    Site contact: Paul Orchard, MD

Study contacts (from the official record)

  • Jake Wesley, PharmD, MS · jake.wesley@immusoft.com
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ISP-001: Sleeping Beauty Transposon-Engineered B Cells for MPS I (NCT05682144) | Bored Studies