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Not yet recruitingNCT07803432Updated Sep 10, 2026

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

An observational study in Hutchinson-Gilford Progeria Syndrome, sponsored by Bundang CHA Hospital. Not yet recruiting. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by Bundang CHA Hospital · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
1
Sex
All
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Study summary

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.

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Conditions studied

  • Hutchinson-Gilford Progeria Syndrome
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In context

Lead sponsor

Bundang CHA Hospital is the lead sponsor of 35 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Non-probability sample

Study 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.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Clinically diagnosed with Hutchinson-Gilford Progeria Syndrome (HGPS) Currently followed as an outpatient at the study institution 19 years of age or younger at enrollment Able to provide written (or legal guardian able to provide consent on the patient's behalf) Willing and able to undergo a single peripheral blood draw for PBMC collection

Exclusion criteria

Exclusion Criteria

Clinical condition precluding safe blood collection (e.g., severe anemia, active infection at the collection site, or a bleeding disorder) Patient or legal guardian unable or unwilling to provide Collected PBMCs yield insufficient quantity or viability for successful iPSC reprogramming (results in post-hoc exclusion from cell-based analysis only, not from study consent)

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
1 participant (estimated)
Target follow-up
1 Year
Patient registry
Yes
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What researchers measure

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

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07803432
Lead sponsor
Bundang CHA Hospital
Collaborators
Korea Research Institute of Bioscience & Biotechnology
Responsible party
MinYoung Kim, MD, PhD (Professor, Department of Rehabilitation Medicine, CHA Bundang Medical Center, Bundang CHA Hospital) — Principal investigator
First posted
Sep 3, 2026
Start date
Oct 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Dec 2029 (estimated)
Last update
Sep 10, 2026

Study contacts

MinYoung Kim
Contact
kmin@cha.ac.kr
82-31-780-6281

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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