An interventional study of Biological - skin biopsy, blood draw, or urine collection for iPSC generation in Diabetes, sponsored by Ospedale San Raffaele. Recruiting at 1 site in Italy. Open to participants aged 12 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-18.
Sponsored by Ospedale San Raffaele · Not applicable, Interventional, and Basic science
The goal of this interventional study is to generate induced pluripotent stem cells (iPSCs) from somatic cells and differentiate them into insulin-producing β cells in patients with metabolic and genetic pancreatic diseases and in healthy controls. The main questions it aims to answer are:
Can somatic cells from healthy individuals and patients with diabetes be successfully reprogrammed into iPSCs?
Can these iPSCs be differentiated into functional insulin-producing β cells suitable for studying disease mechanisms and developing cell-based therapies?
Participants will provide a single biological sample (either a 3 mm skin punch biopsy, a blood sample, or a urine sample) collected under sterile conditions. The samples will be used to derive somatic cells, which will then be reprogrammed into iPSCs and differentiated into β cells for laboratory analyses.
Participants will:
Undergo a one-time sample collection (skin biopsy, blood draw, or urine collection) at Ospedale San Raffaele
Receive standard post-procedure care (if applicable)
This research aims to improve understanding of β cell function and dysfunction in diabetes and to advance personalized regenerative therapies for β cell replacement.
The goal of this interventional study is to investigate how induced pluripotent stem cells (iPSCs) can be efficiently generated from somatic cells and subsequently differentiated into insulin-producing β cells, with the broader aim of improving the understanding of pancreatic β cell biology and supporting the development of future cell-based therapies for diabetes. The study involves the collection of biological samples from both healthy donors and patients affected by metabolic or genetic disorders that impact pancreatic β cell function, such as type 1 diabetes, type 2 diabetes, Maturity Onset Diabetes of the Young (MODY), Wolfram syndrome, and pancreatogenic diabetes.
The primary objective is to establish a reliable and reproducible protocol for the production of iPSCs from somatic cells obtained from different donor groups and to evaluate their potential to differentiate into functional β cells. By comparing iPSC-derived β cells from patients with those derived from healthy controls, the study aims to identify disease-specific cellular and molecular characteristics that may contribute to β cell dysfunction and diabetes pathogenesis. These findings will serve as a foundation for improving strategies for β cell replacement and regenerative medicine.
Participants enrolled in the study will provide a single biological sample, collected at Ospedale San Raffaele in Milan. Depending on the laboratory's technical requirements and the participant's clinical condition, the sample may consist of a 3 mm skin punch biopsy, a small volume of peripheral blood (up to 20 mL), or a urine sample (up to 300 mL). These procedures are all standard clinical techniques performed under sterile conditions by trained healthcare personnel. The risks associated with the procedures are minimal and limited to mild pain, bruising, or, in the case of skin biopsy, a small scar. Participants will receive post-procedure care instructions and will not be required to attend follow-up visits after the sample collection.
Once collected, the somatic cells (such as fibroblasts, peripheral blood mononuclear cells, or urine-derived epithelial cells) will be isolated, expanded, and cryopreserved. These cells will then be reprogrammed into iPSCs using a non-integrating RNA-based reprogramming system (StemRNA™ 3rd Gen Reprogramming Kit, Reprocell). The success of the reprogramming process will be assessed by measuring cell viability and the expression of specific pluripotency markers, including SSEA4, OCT4, and NANOG, through flow cytometry. Only iPSC lines that meet predefined quality criteria-viability above 60% and pluripotency marker expression above 80%-will be considered successful and preserved for further use.
Subsequently, the established iPSC lines will be differentiated into insulin-producing β cells through a stepwise process that mimics pancreatic development. The resulting β-like cells will be analyzed for their ability to produce and secrete insulin in response to glucose stimulation, as well as for other molecular and functional properties. The comparison between β cells derived from healthy donors and those from patients with different forms of diabetes will help elucidate the mechanisms underlying β cell dysfunction and loss in these diseases.
The study will include up to 100 participants, both male and female, aged between 12 and 70 years. At least 30% of participants will be healthy controls, while the remaining will represent patients with various types of pancreatic dysfunction. This approach allows the generation of a diverse biobank of patient-specific iPSC lines, which can be used not only for this study but also for future research projects approved by the Ethics Committee. The total duration of the study is estimated at 10 years, reflecting the long-term nature of iPSC generation, differentiation, and characterization.
Although there are no direct medical benefits for participants, the potential societal benefits of this study are significant. The generation of patient-specific iPSCs provides a powerful platform for studying the pathophysiology of diabetes in vitro, enabling the identification of disease mechanisms and testing of new therapeutic strategies in a personalized way. These cells can serve as models to evaluate how genetic background, environmental factors, and disease states affect β cell development and function. In the long term, this research could contribute to the development of advanced regenerative and transplantation-based treatments for diabetes, potentially reducing or eliminating the need for exogenous insulin therapy.
In summary, this study represents an important step toward bridging fundamental stem cell biology with translational applications in diabetes research. By combining patient-specific iPSC technology with cutting-edge differentiation protocols, it aims to create a resource that not only deepens scientific understanding but also supports the development of innovative and personalized therapies for individuals living with diabetes and related metabolic diseases.
8,290 studies on the registry are indexed under Diabetes Mellitus; 1,077 are open to participants now.
This study's planned enrollment of 100 is above the median of 80 across 6,023 interventional studies indexed under Diabetes Mellitus.
Browse Diabetes Mellitus studies →Ospedale San Raffaele is the lead sponsor of 46 studies on the registry; 15 are open to participants now.
Counted across the registry records on this site, refreshed daily.
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.
Age between 12 and 70 years.
Ability and willingness to provide (or assent with parental consent for minors).
Group 1: Individuals diagnosed with pancreatic β cell dysfunction, including but not limited to:
Type 1 Diabetes
Type 2 Diabetes
Maturity Onset Diabetes of the Young (MODY)
Wolfram Syndrome
Pancreatogenic Diabetes
Group 2: Healthy control donors without pancreatic β cell dysfunction.
Pregnant or breastfeeding women may be included if they meet the inclusion criteria.
Exclusion Criteria:
Age below 12 or above 70 years.
Health condition too compromised to allow safe tissue collection (e.g., acute hypoglycemia \<70 mg/dL or hyperglycemia >140 mg/dL at sampling).
Inability or unwillingness to provide /assent.
Active or current cancer treatment.
Known infection with , , or .
Use of medications that may interfere with iPSC generation (e.g., high-dose , immunomodulators), unless approved by investigators.
For participants undergoing skin : bleeding disorders, local skin infection, allergy to anesthetics, or use of anticoagulants.
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.
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.
Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.
Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Cancer (malignancy)
Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.
Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
HIV
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis B tests
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis C tests
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Corticosteroids (steroids)
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Biopsy and archival tissue
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
All participants will provide a single biological sample (skin biopsy, blood draw, or urine collection) for isolation of somatic cells. These cells will be reprogrammed into induced pluripotent stem cells (iPSCs) and differentiated into insulin-producing β cells to study pancreatic function and disease mechanisms. No therapeutic intervention is administered.
Procedure: Biological - skin biopsy, blood draw, or urine collection for iPSC generation
This study involves a single, minimally invasive biological sampling to obtain somatic cells for the generation of induced pluripotent stem cells (iPSCs). Each participant will undergo only one procedure: a 3 mm skin punch biopsy under local anesthesia, a peripheral blood draw (up to 20 mL), or a urine collection (up to 300 mL), depending on laboratory needs. Samples will be processed to isolate fibroblasts, blood cells, or urine-derived epithelial cells, which will be reprogrammed into iPSCs using a non-integrating RNA-based system . The resulting iPSCs will be characterized for pluripotency and differentiated into insulin-producing β cells.
generation of iPSC
Successful generation of iPSCs from somatic cells, defined by \>80% expression of pluripotency markers (SSEA4, OCT4, NANOG) within 7-60 days after culture establishment.
Time frame: within 7-60 days after culture establishment
Plan to share: No
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