CTNNB1 Neurodevelopmental SyndromePhase 1/2GAIN-CTNNB1NCT07270549
Gene Replacement Therapy for Treatment of Paediatric Patients With CTNNB1 Neurodevelopmental Syndrome
A Phase 1/2 study testing Urbagen gene addition therapy, Sirolimus and Methylprednisolone (Corticosteroid) in people with CTNNB1 Neurodevelopmental Syndrome, run by CTNNB1 Foundation at 1 site in Slovenia.
Trial summary
The goal of this first in human, phase I/II clinical trial is to evaulate the safety, tolerability, and preliminary efficacy of AAV9 mediated gene replacement therapy (Urbagen) in paediatric patients with CTNNB1 neurodevelopmental disorder. Read more about this study
- Who is it for?
- Ages 2 to 12 years
- Conditions the study is for
- CTNNB1 Neurodevelopmental Syndrome
- What is being tested?
- Urbagen gene addition therapy, Sirolimus and Methylprednisolone (Corticosteroid)
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 12 participants
- Where
- 1 siteSlovenia
- Study dates
- 1 Nov 2025to 31 Dec 2032
- Phase
- Phase 1/2
- 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 2 to 12 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Male or female participant aged 2-12 years at the time of informed consent (Part A: 6-12 years, Part B: 2-12 years).
- Child aged 4 to 12 years has to weigh at least 13,3 kg: 5,0E+14 vg.
- Child aged 3 years has to weigh at least 11,96 kg: 4,5E+14 vg.
- Child aged 2 years has to weigh at least 10,94 kg: 4,11E+14 vg.
- Genetically confirmed diagnosis of CTNNB1 syndrome with a heterozygous pathogenic or likely pathogenic variant in the CTNNB1 gene (Class 4/5 according to American College of Medical Genetics and Genomics), confirmed by geneticist at screening.
- Informed consent from the parents/legal guardians of the participant.
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- Parents/legal guardians are willing and able to comply with all protocol visits and procedures.
- Parents/legal guardians are willing and able to reside within 1 hour of the site at which the clinical trial will be conducted for at least 4 months post-dosing. Parents/legal guardians will be informed that this period may be increased in the case of a safety event or concern.
- Parents/legal guardians must agree for the participant not to participate in any other interventional study whilst enrolled in this clinical trial.
- Investigator will check vaccination status of each participant and evaluate and confirm its appropriateness per age and participant's home country. The last vaccination dose must be received a minimum of 30 days prior to the start of immunosuppressants.
- Female participants who are post-menarcheal must have a negative urine pregnancy test at screening and and be willing to have additional pregnancy tests during the study.
- Participant's parents/legal guardians must agree to refrain from future donation of the participant's blood, blood products, tissue, and organs after receiving the IMP due to theoretical risks associated with AAV genome persistence in tissues.
- Participant's use of concomitant medications must be stable for at least 28 days prior to IMP dosing.
Who cannot join
- Participant has a mutation in the CTNNB1 gene which is predicted to result in a gain-of-function effect (e.g. p.G575R) or dominant negative effect (e.g. p.Y333*, p.Q193*, p.A317Vfs8* and p.S352fs*) on the Wnt/β-catenin pathway, or any variant that, in the opinion of the PI, is inconsistent with the mechanism of action of the gene replacement therapy.
- Participant has a concomitant genetic diagnosis or neurodevelopmental syndrome that in the opinion of the investigator could interfere with safety, ability to perform assessments, or data interpretation.
- Participant tests positive for AAV9 antibody with titers >1:50 for AAV9 antibodies utilizing an enzyme linked immunospot.
- Participant has a known allergy or hypersensitivity to any ingredients or excipients of the IMP, or to immunosuppressants or pre-medications specified within the trial protocol.
- Participant with a history of receiving immune-modulating agents (such as chemotherapy, radiotherapy, intravenous steroids, other immunosuppressive agents) within 3 months prior to dosing. Topical or inhaled corticosteroid treatment may be permitted at the discretion of the investigator.
- Participant has a significant concurrent illness or infection within 30 days prior to dosing which could compromise safety.
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- Participant screens positive for acute Coronavirus disease 2019 (COVID-19), confirmed with PCR from a pharyngeal swab sample.
- Participant has serologic evidence of current human immunodeficiency virus (HIV)-1 or HIV-2 infection.
- Participant has acute or chronic hepatitis B or C infections, including:
- Serologic evidence of hepatitis C infection (positive core antibody)
- Serologic evidence of acute or chronic active hepatitis B (positive core antibody and/or positive surface antigen)
- Participant diagnosed with a concomitant neurodevelopmental disorder unrelated to CTNNB1.
- Participant with congenital malformation(s) significantly affecting the nervous system.
- Participant with a history of traumatic, metabolic, vascular or infective brain injury with persistent neurological deficits per investigator's judgement.
- Participant has contraindications for MRI brain.
- Participant has a clinically significant increase in seizure frequency as determined by the investigator or clinically documented episode of generalized status epilepticus (≥30 minute generalized tonic-clonic seizure) within 4 weeks of the baseline visit.
- Participant has severe contractures, as determined by the investigator at screening, which are considered likely to interfere with their ability to complete assessments of motor function.
- Participant has increased intracranial pressure, tumor, vascular abnormality, or any major structural anomaly which could complicate or increase the risk of ICV administration of the IMP. Or the participant has any other contraindication to the ICV procedure.
- Participant has a significant congenital cardiac defect that according to the investigator represents a significant safety risk.
- Participant has a left ventricular ejection fraction (LVEF) < 50% on echocardiogram on previous assessment or at screening.
- Participants with clinically significant cardiovascular abnormalities, including clinically significantly prolonged QT interval in ECG (QT interval corrected using Fridericia's formula (QTcF) ≥ 450 ms at screening).
- Participant is assessed as being unable to tolerate anesthesia required for ICV administration and/or sedation required for other study procedures.
- Participant requiring invasive ventilatory support (e.g. endotracheal ventilation or tracheostomy) within the 6 months prior to enrolment.
- Participant has clinically significant liver disease, defined as any of:
- Aspartate aminotransferase >3,0 x ULN (Grade 1 CTCAE v5.0)
- Alanine aminotransferase >3,0 x ULN (Grade 1 CTCAE v5.0)
- Gamma-glutamyl transferase >2,5 x ULN (Grade 1 CTCAE v5.0)
- Bilirubin >1,5 x ULN (Grade 1 CTCAE v5.0)
- Clinically significant structural abnormality on liver ultrasound.
- Participant has clinically significant renal disease or impairment that could affect safety:
- Creatinine (>1,5 ULN) (Grade 1 CTCAE v5.0)
- GFR <50% LLN (Grade 1 CTCAE v5.0)
- Clinically significant structural abnormality on kidney ultrasound.
- Participant has any of the following abnormal, clinically significant laboratory test results during screening. A single repeat will be permitted.
- Significant thrombocytopenia (Platelet count <150 x 109/L)
- Neutropenia (Absolute neutrophil count <1 x 109/L)
- Persistent leukopenia: <2 x 109/L or leukocytosis: >20 x 109/L
- Significant anemia (hemoglobin <100 g/L)
- Abnormal coagulation (prothrombin time or partial thromboplastin time above ULN)
- Participant has a history of a biopsy-confirmed malignancy.
- Participant has a history of major surgery within six months prior to enrolment or planned surgery during first 12 months of study.
- Participant has any other significant concomitant medical disorder which could confound the interpretation of safety or efficacy data as determined by PI or medical monitor.
- Participant has been enrolled in another interventional clinical trial within 1 year prior to enrolment.
- Participant has previously received gene or cell therapy.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Slovenia1 site, 1 recruiting
- Recruiting
University Medical Centre Ljubljana
Ljubljana, 1000
Damjan Osredkar, MD, PhD, 0038615229273, gain@ctnnb1-foundation.org
Damjan Osredkar, MD, PhD
About this study
Official title: GAIN-CTNNB1: A Phase I/II Open-Label Trial To Evaluate the Safety, Tolerability, and Preliminary Efficacy of Intracerebroventricular Administration of an AAV9 Based Gene Replacement Therapy in Paediatric Patients With CTNNB1 Neurodevelopmental Syndrome
The goal of this first in human, phase I/II clinical trial is to evaulate the safety, tolerability, and preliminary efficacy of AAV9 mediated gene replacement therapy (Urbagen) in paediatric patients with CTNNB1 neurodevelopmental disorder. The main questions it aims to answer are:
- Is the gene therapy with Urbagen safe and well tolerated?
- Does the gene therapy improve motor function, cognitive function, behavior, sleep, and/or quality of life?
Read more
Participants will:
- Undergo screening assessments to ensure eligibility.
- Recieve a single dose of gene therapy via bilateral intracerebroventricular administration.
- Recieve prophylactic immunosuppresants (methylprednisolone, sirolimus).
- Attend follow-up visits for safety monitoring and clinical assessments over the course of three years.
Read the detailed description
CTNNB1 syndrome is a severe monogenic neurodevelopmental disorder caused by de novo mutations in the CTNNB1 gene. It presents with global developmental delay, spastic dystonic motor impairment, intellectual disability, absent or minimal speech, and a high prevalence of autistic traits.
Urbagen is an investigational gene addition therapy designed to restore functional CTNNB1 expression and improve neurological and developmental outcomes in affected patients. It is a recombinant, single-stranded adeno-associated viral vector serotype 9 (AAV9) encoding the human CTNNB1 gene under the control of the cytomegalovirus enhancer/chicken-β actin hybrid (CBh) promoter. The AAV9 vector facilitates targeted delivery to the central nervous system (CNS), crossing the blood-brain barrier (BBB) and ensuring localized gene expression to address the neurological deficits associated with CTNNB1 syndrome. The therapy is designed as a single-dose bilateral intracerebroventricular (ICV) infusion. The ICV route was selected based on its ability to achieve widespread CNS transduction while minimizing peripheral exposure, as demonstrated in preclinical models.
The goal of this first in human, phase I/II clinical trial to establish the safety, tolerability, and preliminary efficacy of AAV9 mediated gene replacement therapy (Urbagen) in paediatric patients with CTNNB1 syndrome. Urbagen has received orphan drug designation by European Medicines Agency (EMA). The clinical trial was approved by EMA/JAZMP.
This is a monocentric trial conducted at the University Children's Hospital, University Medical Centre Ljubljana, Slovenia. Twelve international participants will receive a single dose of Urbagen via bilateral intracerebroventricular administration. Prophylactic immunosuppresants (methylprednisolone, sirolimus) will be used to reduce the risks of immune-mediated complicationts. Participants will be assessed with a variety of tests during the screening and follow-up period with a total follow up of 5 years.
- Conditions
- CTNNB1 Neurodevelopmental Syndrome
- Being tested
- Urbagen gene addition therapy, Sirolimus, Methylprednisolone (Corticosteroid)
- Keywords
- CTNNB1 neurodevelopmental syndrome, AAV9 mediated gene replacement therapy, Gene replacement therapy, Gene addition therapy, Gene therapy, Clinical trial
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Urbagen gene addition therapyBiological
Urbagen is a non-replicating single-stranded adeno-associated viral vector 9 encoding for the human β-catenin protein (AAV9/hCTNNB1 vector). It is administered as a single bilateral ICV infusion.
SirolimusDrug
The use of sirolimus will be consistent with other AAV-9 gene therapy protocols. On Day -7 prior to the administration of URBAGEN, participants will receive a loading dose of sirolimus (3 doses of 1 mg/m2 every four hours). The following day, participants will begin a maintenance dose of sirolimus (0,5 mg/m2/day in 2 divided doses daily), which they will continue for a minimum of 10 months.
Methylprednisolone (Corticosteroid)Drug
The use of methylprednisolone will be consistent with other AAV-9 gene therapy protocols. On the day of dosing (Day 0), participants will receive a dose of IV methylprednisolone (10 mg/kg to a maximum single dose of 500 mg, infused over 30 minutes). On Day -1 prior to administration of URBAGEN, participants will begin a course of oral prednisolone (1,0 mg/kg/day, maximum dose 30 mg daily). Prednisolone administration will continue for a minimum of four months, followed by a gradual tapering schedule.
| Study group | Role | What they receive |
|---|---|---|
| Treatment arm | Experimental | Urbagen, an AAV-9 mediated gene addition therapy Receives: Biological: Urbagen gene addition therapy; Drug: Sirolimus; Drug: Methylprednisolone (Corticosteroid) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Monitoring for treatment-emergent adverse events and serious adverse events in all participants.
Measured: 5 years (multiple timepoints)
Secondary outcomes (13)
Improvement in motor function as measured by the Bayley Scale of Infant Development 4.
The Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley-4), is a standardized assessment used to evaluate developmental functioning in infants and young children across cognitive, language, and motor domains. Composite scores are standardized with a mean of 100 and a standard deviation of 15, typically ranging from 40 to 160. Higher scores indicate better developmental performance, while lower scores reflect increasing levels of developmental delay.
Measured: 5 years (multiple timepoints)
Improvement in motor function as measured by the Wearable Syde Device (in ambulant patients).
Syde Wearable Device is a digital sensor system used to objectively monitor motor function in children and adults, particularly in neuromuscular disorders. It continuously records movement data such as stride length, velocity, and limb activity during daily life. Specific endpoints, such as the Stride Velocity 95th Centile (SV95C), are derived from the recorded data. Higher values of SV95C indicate better motor performance, whereas lower values reflect greater functional impairment and a worse outcome.
Measured: 5 years (multiple timepoints)
Improvement in dystonia as measured by the Burke-Fahn-Marsden Dystonia Rating Scale.
The Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) is a quantitative measure of dystonia severity used in both children and adults. A score of 0 indicates the absence of dystonia in all assessed body regions, whereas the maximum score of 120 reflects severe dystonia affecting all assessed body regions, even at rest.
Measured: 5 years (multiple timepoints)
Improvement in spasticity as measured by the 13-item Spastic Paraplegia Rating Scale.
The Spastic Paraplegia Rating Scale (SPRS) assesses functional impairment in children and adults with spastic paraplegia. A score of 0 indicates the absence of disease manifestation, whereas the maximum score of 52 reflects severe disease manifestation.
Measured: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Bayley Scale of Infant Development 4.
The Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley-4), is a standardized assessment used to evaluate developmental functioning in infants and young children across cognitive, language, and motor domains. Composite scores are standardized with a mean of 100 and a standard deviation of 15, typically ranging from 40 to 160. Higher scores indicate better developmental performance, while lower scores reflect increasing levels of developmental delay.
Measured: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Vineland Adaptive Infant Behavior Scale 3.
The Vineland Adaptive Behavior Scales, Third Edition (Vineland-3), is a standardized assessment that measures adaptive functioning in infants, children, and adults across communication, daily living skills, socialization, and motor domains. Adaptive Behavior Composite scores are standardized with a mean of 100 and a standard deviation of 15, typically ranging from 20 to 160. Higher scores indicate better adaptive functioning, whereas lower scores reflect greater impairment in adaptive behavior.
Measured: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Wechsler Non-Verbal Intelligence Scale.
The Wechsler Nonverbal Scale of Ability (WNV) is a standardized assessment of nonverbal cognitive functioning designed for children and adolescents, particularly those with language impairments. Scores are reported as a standard score with a mean of 100 and a standard deviation of 15, typically ranging from 40 to 160. Higher scores indicate better nonverbal intellectual ability, whereas lower scores reflect greater cognitive impairment.
Measured: 5 years (multiple timepoints)
Improvement in communication as measured by the Vineland Adaptive Scale 3.
The Vineland Adaptive Behavior Scales, Third Edition (Vineland-3), is a standardized assessment that measures adaptive functioning in infants, children, and adults across communication, daily living skills, socialization, and motor domains. Adaptive Behavior Composite scores are standardized with a mean of 100 and a standard deviation of 15, typically ranging from 20 to 160. Higher scores indicate better adaptive functioning, whereas lower scores reflect greater impairment in adaptive behavior.
Measured: 5 years (multiple timepoints)
Behavioral Improvement measured by the Aberrant Behavior Checklist.
The Aberrant Behavior Checklist (ABC) is a caregiver-reported assessment used to evaluate problem behaviors in children and adults with developmental and intellectual disabilities. It consists of five subscales (irritability, lethargy/social withdrawal, stereotypic behavior, hyperactivity/noncompliance, and inappropriate speech) with a total score ranging from 0 to 174. A score of 0 indicates the absence of aberrant behaviors, whereas higher scores reflect increasing severity and frequency of behavioral problems.
Measured: 5 years (multiple timepoints)
Behavioral Improvement measured by the M-CHAT or Autism Spectrum Quotient (depending on the participant's age).
The Modified Checklist for Autism in Toddlers (M-CHAT) is a caregiver-completed screening tool used to identify children at risk for autism spectrum disorder. Scores range from 0 to 20, with lower scores indicating typical development and higher scores reflecting an increased risk for autism spectrum disorder and a worse outcome.
The Autism-Spectrum Quotient (AQ) is a self-report questionnaire designed to measure the degree of autistic traits in children and adolescents. It consists of 50 items, yielding a total score ranging from 0 to 50. Lower scores indicate fewer autistic traits, whereas higher scores reflect a greater number of autistic traits.
Measured: 5 years (multiple timepoints)
Improvement in sleep as measured by the Bruni Sleep Disturbance Scale.
The Bruni Sleep Disturbance Scale for Children (SDSC) is a caregiver-reported questionnaire used to evaluate sleep disturbances in children. It consists of 26 items across six subscales, with a total score ranging from 26 to 130. Lower scores indicate fewer sleep problems, while higher scores reflect more severe sleep disturbances.
Measured: 5 years (multiple timepoints)
Improvement in epilepsy as measured by seizure frequency.
Measured: 5 years (multiple timepoints)
Improvement in Quality of Life as measured by Pediatric QOL Inventory - Family and Core module (age appropriate).
The Pediatric Quality of Life Inventory (PedsQL) Core and Family Impact Modules are standardized questionnaires used to assess health-related quality of life in children and the impact of pediatric health conditions on family functioning. Scores are transformed to a 0-100 scale, where 0 represents the poorest quality of life and 100 represents the best possible quality of life.
Measured: 5 years (multiple timepoints)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Dec 2025
- Study start1 Nov 2025
- Primary completion31 Dec 2032 (estimated)
- Study completion31 Dec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for CTNNB1 Neurodevelopmental SyndromeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 1/2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 12 participants (estimated)
Sponsor and investigators
- Lead sponsor
- CTNNB1 Foundation
- Sponsor type
- University, hospital or other
- Collaborators
- University Medical Centre Ljubljana
- Responsible party
- Principal investigator, Damjan Osredkar, University Medical Centre Ljubljana
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07270549
- Sponsor's protocol ID
- 0120-536/2025-2711
- Other IDs
- 2025-522719-40-00, 2025
- Acronym
- GAIN-CTNNB1
- Status last verified
- Mar 2026
- First submitted
- 14 Nov 2025
- Last updated
- 25 Mar 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Zakelj N, Gosar D, Mirosevic S, Sanders SJ, Ljungdahl A, Kohani S, Huang S, Leong LI, An Y, Teo MJ, Moultrie F, Jerala R, Lainscek D, Forstneric V, Susjan P, Lisowski L, Perez-Iturralde A, Mrak JO, Chan HYE, Osredkar D. Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome. HGG Adv. 2025 Oct 9;6(4):100483. doi: 10.1016/j.xhgg.2025.100483. Epub 2025 Jul 18.
PubMed 40684264Mirosevic S, Khandelwal S, Amerson E, Parks E, Parks M, Cochran L, Gonzalez Hernandez A, Ferraro M, Lisowski L, Perez-Iturralde A, Chung W, Jacob MH, Zakelj N, Lainscek D, Forstneric V, Susjan P, Maruna M, Jerala R, Osredkar D. Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective. Ther Adv Rare Dis. 2025 Feb 12;6:26330040251318355. doi: 10.1177/26330040251318355. eCollection 2025 Jan-Dec.
PubMed 39949392Mirosevic S, Khandelwal S, Susjan P, Zakelj N, Gosar D, Forstneric V, Lainscek D, Jerala R, Osredkar D. Correlation between Phenotype and Genotype in CTNNB1 Syndrome: A Systematic Review of the Literature. Int J Mol Sci. 2022 Oct 19;23(20):12564. doi: 10.3390/ijms232012564.
PubMed 36293418Parichha A, Datta D, Singh A, Talwar I, Yadav S, Bose M, Suresh V, Mirosevic S, Zakelj N, Gosar D, Osredkar D, Tole S. An evolutionarily conserved role for CTNNB1/beta-CATENIN in regulating the development of the corpus callosum. iScience. 2025 Aug 9;28(9):113335. doi: 10.1016/j.isci.2025.113335. eCollection 2025 Sep 19.
PubMed 40894864Arkar Silan U, Trebse A, Kovac J, Rogac M, Troha Gergeli A, Sket R, Bregant T, Neubauer D, Peterlin B, Osredkar D. Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohort. Front Neurol. 2025 Jul 23;16:1615449. doi: 10.3389/fneur.2025.1615449. eCollection 2025.
PubMed 40771987Groselj U, Kavcic M, Drole Torkar A, Kafol J, Lainscek D, Jerala R, Sever M, Zver S, Sersa G, Cemazar M, Strojan P, Groselj A, Zerjav Tansek M, Mirosevic S, Ivancan S, Prelog T, Gosar D, Orazem Mrak J, Mlinaric M, Bertok S, Kovac J, Kodric J, Battelino S, Pokorn M, Ihan A, Jazbec J, Battelino T, Osredkar D. Gene therapy of rare diseases as a milestone in medicine - overview of the field and report on initial experiences in Slovenia. Orphanet J Rare Dis. 2025 Jun 5;20(1):279. doi: 10.1186/s13023-025-03828-8.
PubMed 40474241
Study at a glance
From the registry record, last updated by the sponsor on 25 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- GAIN-CTNNB1: A Phase I/II Open-Label Trial To Evaluate the Safety, Tolerability, and Preliminary Efficacy of Intracerebroventricular Administration of an AAV9 Based Gene Replacement Therapy in Paediatric Patients With CTNNB1 Neurodevelopmental Syndrome
- ClinicalTrials.gov ID
- NCT07270549
- Acronym / sponsor ID
- GAIN-CTNNB1 / 0120-536/2025-2711
- Conditions
- CTNNB1 Neurodevelopmental Syndrome
- Keywords
- CTNNB1 neurodevelopmental syndrome, AAV9 mediated gene replacement therapy, Gene replacement therapy, Gene addition therapy, Gene therapy, Clinical trial
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 12 participants (estimated)
- Lead sponsor
- CTNNB1 FoundationUniversity, hospital or other
- Collaborators
- University Medical Centre Ljubljana
- Study start
- 1 Nov 2025 (actual)
- Primary completion
- 31 Dec 2032 (estimated)
- Study completion
- 31 Dec 2032 (estimated)
- First posted
- 8 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this first in human, phase I/II clinical trial is to evaulate the safety, tolerability, and preliminary efficacy of AAV9 mediated gene replacement therapy (Urbagen) in paediatric patients with CTNNB1 neurodevelopmental disorder. The main questions it aims to answer are:
- Is the gene therapy with Urbagen safe and well tolerated?
- Does the gene therapy improve motor function, cognitive function, behavior, sleep, and/or quality of life?
Participants will:
- Undergo screening assessments to ensure eligibility.
- Recieve a single dose of gene therapy via bilateral intracerebroventricular administration.
- Recieve prophylactic immunosuppresants (methylprednisolone, sirolimus).
- Attend follow-up visits for safety monitoring and clinical assessments over the course of three years.
Detailed description
CTNNB1 syndrome is a severe monogenic neurodevelopmental disorder caused by de novo mutations in the CTNNB1 gene. It presents with global developmental delay, spastic dystonic motor impairment, intellectual disability, absent or minimal speech, and a high prevalence of autistic traits.
Urbagen is an investigational gene addition therapy designed to restore functional CTNNB1 expression and improve neurological and developmental outcomes in affected patients. It is a recombinant, single-stranded adeno-associated viral vector serotype 9 (AAV9) encoding the human CTNNB1 gene under the control of the cytomegalovirus enhancer/chicken-β actin hybrid (CBh) promoter. The AAV9 vector facilitates targeted delivery to the central nervous system (CNS), crossing the blood-brain barrier (BBB) and ensuring localized gene expression to address the neurological deficits associated with CTNNB1 syndrome. The therapy is designed as a single-dose bilateral intracerebroventricular (ICV) infusion. The ICV route was selected based on its ability to achieve widespread CNS transduction while minimizing peripheral exposure, as demonstrated in preclinical models.
The goal of this first in human, phase I/II clinical trial to establish the safety, tolerability, and preliminary efficacy of AAV9 mediated gene replacement therapy (Urbagen) in paediatric patients with CTNNB1 syndrome. Urbagen has received orphan drug designation by European Medicines Agency (EMA). The clinical trial was approved by EMA/JAZMP.
This is a monocentric trial conducted at the University Children's Hospital, University Medical Centre Ljubljana, Slovenia. Twelve international participants will receive a single dose of Urbagen via bilateral intracerebroventricular administration. Prophylactic immunosuppresants (methylprednisolone, sirolimus) will be used to reduce the risks of immune-mediated complicationts. Participants will be assessed with a variety of tests during the screening and follow-up period with a total follow up of 5 years.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Treatment arm | Experimental | Biological: Urbagen gene addition therapy, Drug: Sirolimus, Drug: Methylprednisolone (Corticosteroid)Urbagen, an AAV-9 mediated gene addition therapy |
Who may qualify
- Ages
- 2 to 12 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (13 listed)
- Male or female participant aged 2-12 years at the time of informed consent (Part A: 6-12 years, Part B: 2-12 years).
- Child aged 4 to 12 years has to weigh at least 13,3 kg: 5,0E+14 vg.
- Child aged 3 years has to weigh at least 11,96 kg: 4,5E+14 vg.
- Child aged 2 years has to weigh at least 10,94 kg: 4,11E+14 vg.
- Genetically confirmed diagnosis of CTNNB1 syndrome with a heterozygous pathogenic or likely pathogenic variant in the CTNNB1 gene (Class 4/5 according to American College of Medical Genetics and Genomics), confirmed by geneticist at screening.
Key exclusion criteria (44 listed)
- Participant has a mutation in the CTNNB1 gene which is predicted to result in a gain-of-function effect (e.g. p.G575R) or dominant negative effect (e.g. p.Y333*, p.Q193*, p.A317Vfs8* and p.S352fs*) on the Wnt/β-catenin pathway, or any variant that, in the opinion of the PI, is inconsistent with the mechanism of action of the gene replacement therapy.
- Participant has a concomitant genetic diagnosis or neurodevelopmental syndrome that in the opinion of the investigator could interfere with safety, ability to perform assessments, or data interpretation.
- Participant tests positive for AAV9 antibody with titers >1:50 for AAV9 antibodies utilizing an enzyme linked immunospot.
- Participant has a known allergy or hypersensitivity to any ingredients or excipients of the IMP, or to immunosuppressants or pre-medications specified within the trial protocol.
- Participant with a history of receiving immune-modulating agents (such as chemotherapy, radiotherapy, intravenous steroids, other immunosuppressive agents) within 3 months prior to dosing. Topical or inhaled corticosteroid treatment may be permitted at the discretion of the investigator.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Urbagen gene addition therapyUrbagen is a non-replicating single-stranded adeno-associated viral vector 9 encoding for the human β-catenin protein (AAV9/hCTNNB1 vector). It is administered as a single bilateral ICV infusion. | Biological | Treatment arm |
| SirolimusThe use of sirolimus will be consistent with other AAV-9 gene therapy protocols. On Day -7 prior to the administration of URBAGEN, participants will receive a loading dose of sirolimus (3 doses of 1 mg/m2 every four hours). The following day, participants will begin a maintenance dose of sirolimus (0,5 mg/m2/day in 2 divided doses daily), which they will continue for a minimum of 10 months. | Drug | Treatment arm |
| Methylprednisolone (Corticosteroid)The use of methylprednisolone will be consistent with other AAV-9 gene therapy protocols. On the day of dosing (Day 0), participants will receive a dose of IV methylprednisolone (10 mg/kg to a maximum single dose of 500 mg, infused over 30 minutes). On Day -1 prior to administration of URBAGEN, participants will begin a course of oral prednisolone (1,0 mg/kg/day, maximum dose 30 mg daily). Prednisolone administration will continue for a minimum of four months, followed by a gradual tapering schedule. | Drug | Treatment arm |
Primary outcome
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Time frame: 5 years (multiple timepoints)
Monitoring for treatment-emergent adverse events and serious adverse events in all participants.
13 secondary outcomes
Improvement in motor function as measured by the Bayley Scale of Infant Development 4.
Time frame: 5 years (multiple timepoints)
Improvement in motor function as measured by the Wearable Syde Device (in ambulant patients).
Time frame: 5 years (multiple timepoints)
Improvement in dystonia as measured by the Burke-Fahn-Marsden Dystonia Rating Scale.
Time frame: 5 years (multiple timepoints)
Improvement in spasticity as measured by the 13-item Spastic Paraplegia Rating Scale.
Time frame: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Bayley Scale of Infant Development 4.
Time frame: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Vineland Adaptive Infant Behavior Scale 3.
Time frame: 5 years (multiple timepoints)
Improvement in cognitive function as measured by the Wechsler Non-Verbal Intelligence Scale.
Time frame: 5 years (multiple timepoints)
Improvement in communication as measured by the Vineland Adaptive Scale 3.
Time frame: 5 years (multiple timepoints)
Behavioral Improvement measured by the Aberrant Behavior Checklist.
Time frame: 5 years (multiple timepoints)
Behavioral Improvement measured by the M-CHAT or Autism Spectrum Quotient (depending on the participant's age).
Time frame: 5 years (multiple timepoints)
Improvement in sleep as measured by the Bruni Sleep Disturbance Scale.
Time frame: 5 years (multiple timepoints)
Improvement in epilepsy as measured by seizure frequency.
Time frame: 5 years (multiple timepoints)
Improvement in Quality of Life as measured by Pediatric QOL Inventory - Family and Core module (age appropriate).
Time frame: 5 years (multiple timepoints)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Mar 2026.
- Background: PubMed 40684264Zakelj N, Gosar D, Mirosevic S, Sanders SJ, Ljungdahl A, Kohani S, Huang S, Leong LI, An Y, Teo MJ, Moultrie F, Jerala R, Lainscek D, Forstneric V, Susjan P, Lisowski L, Perez-Iturralde A, Mrak JO, Chan HYE, Osredkar D. Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome. HGG Adv. 2025 Oct 9;6(4):100483. doi: 10.1016/j.xhgg.2025.100483. Epub 2025 Jul 18.
- Background: PubMed 39949392Mirosevic S, Khandelwal S, Amerson E, Parks E, Parks M, Cochran L, Gonzalez Hernandez A, Ferraro M, Lisowski L, Perez-Iturralde A, Chung W, Jacob MH, Zakelj N, Lainscek D, Forstneric V, Susjan P, Maruna M, Jerala R, Osredkar D. Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective. Ther Adv Rare Dis. 2025 Feb 12;6:26330040251318355. doi: 10.1177/26330040251318355. eCollection 2025 Jan-Dec.
- Background: PubMed 36293418Mirosevic S, Khandelwal S, Susjan P, Zakelj N, Gosar D, Forstneric V, Lainscek D, Jerala R, Osredkar D. Correlation between Phenotype and Genotype in CTNNB1 Syndrome: A Systematic Review of the Literature. Int J Mol Sci. 2022 Oct 19;23(20):12564. doi: 10.3390/ijms232012564.
- Background: PubMed 40894864Parichha A, Datta D, Singh A, Talwar I, Yadav S, Bose M, Suresh V, Mirosevic S, Zakelj N, Gosar D, Osredkar D, Tole S. An evolutionarily conserved role for CTNNB1/beta-CATENIN in regulating the development of the corpus callosum. iScience. 2025 Aug 9;28(9):113335. doi: 10.1016/j.isci.2025.113335. eCollection 2025 Sep 19.
- Background: PubMed 40771987Arkar Silan U, Trebse A, Kovac J, Rogac M, Troha Gergeli A, Sket R, Bregant T, Neubauer D, Peterlin B, Osredkar D. Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohort. Front Neurol. 2025 Jul 23;16:1615449. doi: 10.3389/fneur.2025.1615449. eCollection 2025.
- Background: PubMed 40474241Groselj U, Kavcic M, Drole Torkar A, Kafol J, Lainscek D, Jerala R, Sever M, Zver S, Sersa G, Cemazar M, Strojan P, Groselj A, Zerjav Tansek M, Mirosevic S, Ivancan S, Prelog T, Gosar D, Orazem Mrak J, Mlinaric M, Bertok S, Kovac J, Kodric J, Battelino S, Pokorn M, Ihan A, Jazbec J, Battelino T, Osredkar D. Gene therapy of rare diseases as a milestone in medicine - overview of the field and report on initial experiences in Slovenia. Orphanet J Rare Dis. 2025 Jun 5;20(1):279. doi: 10.1186/s13023-025-03828-8.
- CTNNB1 FoundationLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing Urbagen gene addition therapy, Sirolimus and Methylprednisolone (Corticosteroid) in people with CTNNB1 Neurodevelopmental Syndrome, run by CTNNB1 Foundation at 1 site in Slovenia.
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 13 inclusion and 44 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: looking for participants now, as of the sponsor's last update on 25 Mar 2026. 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 Slovenia. 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.
What does this combined phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Contact Damjan Osredkar, MD, PhD (0038615229273, gain@ctnnb1-foundation.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] (time frame: 5 years (multiple timepoints)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07270549, which also lists 6 linked publications.
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 25 Mar 2026.