Creating Stem Cells From a Progeria Patient's Blood to Test Candidate Treatments in the Lab

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorBundang CHA Hospital

About this trial

This study aims to establish induced pluripotent stem cell (iPSC) lines from the blood of one pediatric patient with Hutchinson-Gilford Progeria Syndrome (HGPS), a rare disease that causes rapid, premature aging, in order to build a laboratory model of the disease. The main purpose of this study is to collect a blood sample (a total of 9cc, drawn once) from the patient, reprogram the patient's blood cells into stem cells, and then differentiate these stem cells into disease-relevant cell types (such as fibroblasts, vascular smooth muscle cells, and neurons) to study how HGPS affects cells at a molecular level. These patient-derived cells will then be used entirely in the laboratory (in-vitro) to test the safety and effectiveness of candidate treatments, including an RNA-targeting gene therapy, before any such therapy would be considered for use in patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

This study will enroll a single pediatric patient with Hutchinson-Gilford Progeria Syndrome (HGPS) who is currently receiving outpatient follow-up care at the Department of Rehabilitation Medicine, CHA Bundang Medical Center. The patient was identified through routine clinical care at this institution; no external recruitment or advertisement will be used.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Established an induced pluripotent stem cell (iPSC) cell line.

Established an induced pluripotent stem cell (iPSC) cell line using peripheral blood mononuclear cells (PBMCs) obtained from patients with Hutchinson-Gilford Progeria Syndrome.

Time frame
Through study completion, an estimated 12 months from PBMC collection

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Bundang CHA Hospital

Lead sponsor

Korea Research Institute of Bioscience & Biotechnology

Collaborator

This trial is not recruiting at the moment. You can still explore other options: