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Alpha1-antitrypsin DeficiencyNCT06892236

Preparation of IPSC for Cell Gene Editing for the Treatment of AATD

A study testing iPSC generation in people with Alpha1-antitrypsin Deficiency, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 1 site in Italy.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Alpha 1-antitrypsin (AAT) deficiency is a genetic condition that leads to lung and/or liver diseases; current treatment of weekly augmentation of AAT addresses only lung diseases with moderate efficacy. Novel treatments based on gene editing can restore physiological levels of AAT and address lung and liver disease. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Alpha1-antitrypsin Deficiency
What is being tested?
iPSC generation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
3 participants
Where
1 siteItaly
Study dates
15 Jan 2025to 28 Feb 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • age ≥ 18 years at the time of signing the ICF
  • diagnosis of severe AATD (2 pathological variants)

Who cannot join

  • incapability to give informed consent
  • subject under augmentation therapy

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Italy1 site
  • Fondazione IRCCS Policlinico San Matteo, Sc Pneumologia

    Pavia, Pavia, 27100

Other trials in Italy

About this study

Official title: Preparation of Large-scale Patient-specific Induced Pluripotent Stem Cells (iPSC) Library for Cell Gene Editing for the Treatment of Alpha1-antitrypsin Deficiency

Alpha 1-antitrypsin (AAT) deficiency is a genetic condition that leads to lung and/or liver diseases; current treatment of weekly augmentation of AAT addresses only lung diseases with moderate efficacy. Novel treatments based on gene editing can restore physiological levels of AAT and address lung and liver disease.

The aim is to generate induced pluripotent stem cells (iPSC) from blood and urine of patients with different severe Alpha1-antitrypsin deficiency (AATD) genotypes. Further, the iPSC will be differentiated into hepatocytes (iHep). Since hepatocytes are the main producers of AAT, the iHep will be used to test different approaches of gene editing to correct various mutations. Gene editing will be conducted at University of Bern (Switzerland)

Read the detailed description

AAT is majorly produced in the hepatocytes therefore correction in the hepatocyte is a most promising approach. iHep cells as well as pluripotent stem cell or mesenchymal stem cell-derived hepatocyte-like cells provide potential cell sources for disease modeling, transplantation, and tissue engineering independent of donor organs.

However, all the studies reported in the literature, including the large drug library screening, are based on one or few AAT variant or at most few hiPSC cell lines derived from AATD patients. Moreover, only a subgroup of 10% of PI*ZZ developed a clinically relevant liver disease and there is a strong suspect that genetic and/or environmental modifiers determine whether an affected homozygote is susceptible to liver disease. Moreover, there is no study about the efficacy of potential drug in reducing cellular AAT accumulation for other AAT genotypes rather than PI*ZZ and for other rare mutations associated with liver inclusions and clinically apparent liver disease. This limitation represents a strong barrier in the development of new therapies. For this reason, the investigators will select candidates with different disease profiles. The investigators plan to recruit patients with different genotypes, including the carriers of rare pathological variants. iPSC will be generated from peripheral blood and urine cells, then cells will be characterised and stored. The PBMC will be frozen and will be reprogrammed to Induced pluripotent stem cells. The derived IPSC will be characterized by standard methods of immunofluroscence, qRTPCR, combined genomic hybridization (CGH) and flowcytometry, and will be differentiated to three germ layers.

Further, the investigators will differentiate iPSC into hepathocytes (iHep). The iPSC derived hepatocytes from the AAT deficient patients will be characterized for the mutations. There have been attempts to develop hepatocyte specific targeting but with limitations therefore in the current proposal the investigators aim at developing and testing two different approaches for cell specific targeting: 1) by hepatocyte specific liposome/virosome by integrating/conjugating asialofeutin on the surface of the liposome/virosomes either as protein fragments or peptides; 2) coating the liposome/virosome carrying the BEs with hepatocyte derived exovesicle surface membrane and delivering the BEs in the AATD iHep to test the feasibility of this method for treatment of AAT deficiency. These hepatocytes will be treated with BEs and its effect will be evaluated by deep sequencing, immunohistochemistry and secretion of AAT will be confirmed by ELISA.

Base editing is an emerging method of precision medicine that the investigators are going to use as treatment to cure AATD. In order to reach the target, the investigators propose here to use extracellular vesicles to deliver base editors in the liver. Extracellular vesicles are secreted by almost all types of cells and can be used as carriers of potential therapeutic proteins. It has been shown that base editing is a very promising technique to correct genetic mutation. However, several challenges remain unresolved and, in this grant, the investigators want to address: specificity, stability, bio-distribution, and analysis of long-term effects.

Being tested
iPSC generation
Medical subject headings
alpha 1-Antitrypsin Deficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • iPSC generationGenetic

    Base editing

Study groups in NCT06892236
Study groupRoleWhat they receive
severe AATD patientsOtherblood samples from severe AATD patients to obtain iPSC cells
Receives: Genetic: iPSC generation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of severe AATD patients included in the study

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Mar 2025
  2. Study start15 Jan 2025
  3. Primary completion28 Feb 2026 (estimated)
  4. Study completion28 Feb 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
3 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06892236
Sponsor's protocol ID
AATD-iPSC
Status last verified
Mar 2025
First submitted
24 Feb 2025
Last updated
24 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing iPSC generation in people with Alpha1-antitrypsin Deficiency, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 24 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of severe AATD patients included in the study (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Mar 2025.

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