Cornelia De Lange SyndromePhase 2/3CLoSERNCT06789783
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment
A Phase 2/3 study testing Lithium Carbonate Capsule in people with Cornelia De Lange Syndrome, run by University of Milan at 1 site in Italy.
Trial summary
The study "Cornelia de Lange Syndrome: assessing positive effects of Lithium treatment - CLoSER" aims to evaluate the effectiveness on behavioral modifications of lithium carbonate therapy in patients with Cornelia de Lange syndrome (CdLS). Read more about this study
- Who is it for?
- Ages 4 years and older
- Conditions the study is for
- Cornelia De Lange Syndrome
- What is being tested?
- Lithium Carbonate Capsule
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 34 participants
- Where
- 1 siteItaly
- Study dates
- 1 May 2024to Dec 2026
- Phase
- Phase 2/3
- 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 4 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Age > 4 years
- Body weight within the normal range in the reference range for CdLS, based on age and height
- Diagnosis of CdLS based on consensus clinical criteria and a confirmed mutation in the NIPBL gene
- Stable drug regimen for 4 weeks prior to starting the study
- Written consent signed by parent/legal guardian/representative prior to the screening visit
- Ability to take the study drug provided in capsules or drops (for younger patients and those with swallowing difficulties) or combined with food/drinks
- Caregiver must be able to understand the instructions and participate knowingly in the study
Who cannot join
- The patient is participating in another clinical trial
- QT interval prolongation, thyroid dysfunction, renal insufficiency, hepatic insufficiency, leukopenia, or other currently clinically significant medical disorders (as determined by the investigator), other than those directly related to CdLS
- QTcF interval on ECG greater than 450 msec
- Severe diabetes mellitus or inherited metabolic disorder
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, 1 recruiting
- Recruiting
University of Milan
Milan, MI
Closer, 0250323207, trialcloser@gmail.com
About this study
The study "Cornelia de Lange Syndrome: assessing positive effects of Lithium treatment - CLoSER" aims to evaluate the effectiveness on behavioral modifications of lithium carbonate therapy in patients with Cornelia de Lange syndrome (CdLS).
CdLS is a rare genetic disease caused by autosomal mutations dominant or X-linked. The prevalence of CdLS is estimated to be between 1:10,000-30,000 newborns, but it is probably underestimated because the most cases mild ones may go undiagnosed. This syndrome is characterized by slow growth before and after birth with intellectual disability and short stature, from major malformations such as facial anomalies, neurological disorders, gastrointestinal and musculoskeletal malformations. To date, for these patients only targeted medical and surgical therapeutic interventions are recommended for improving the quality of life. No drug therapy is validated for the cognitive/behavioral disorders. It has been shown that lihium-dependent activation of the WNT pathway is able to recover the Abnormal phenotype in many CdLS models. Lithium is already widely used in psychiatry and has a long history of clinical efficacy.
Read more
Recently some studies are evaluating the effect of lithium in patients with characteristics common to CdLS showing promising results . This trial intends to transfer the preliminary data obtained from in vitro and in vivo studies on patients with CdLS.
Given the currently untreatable nature of the syndrome, this treatment could represent a possible therapeutic strategy aimed at improving the behavioral and intellectual disabilities typical of CdLS.
Read the detailed description
Research Objectives This study aims to evaluate the effectiveness of lithium carbonate therapy on behavioral changes in patients with Cornelia de Lange syndrome (CdLS). This is a multicenter and non-commercial pilot clinical study.
The specific objectives are the following:
PRIMARY OUTCOME - Improvement in the following parameters:
- Behavior assessed by Aberrant Behavior Checklist (ABC scale1), which measures psychiatric symptoms and behavioral disorders also in patients with intellectual disability;
SECONDARY OUTCOMES - Improvement in the following parameters:
- SCQ questionnaire (SCQ; Rutter, Bailey\&Lord, 20032) to assess communication skills and social functioning;
- Childhood Autism Rating Scale (CARS 2 -T3) to assess autistic behaviors;
- Cognitive Performance through the Leiter scale (Leiter-R, Roid \& Miller, 19974), a non-verbal scale that can be used for subjects between 2 and 20 years old.
- Vineland Adaptive Behavior Scales 2 to evaluate adaptive functioning in the different areas (motor, communication, autonomy, socialization). For severe patients, where a direct evaluation with the Leiter may be insignificant or impossible to conduct, it would provide an adaptation quotient (AQ).
- Sleep quality through the Sleep Disturbances Scale for children (SDSC5), to be administered to parents; there are two versions, one for subjects between 6 and 16 years old, the other for children 3-6 years old;
- Impression of Change Clinical Global Impression of Change (CGI-C) completed by the clinician at each visit;
- Improvement in quality of life through Pediatric Quality of Life Inventory (PedsQL6)
- Specific biomarkers will be used to measure lipid peroxidation in cell extracts, tissues and biological fluids.
Background Cornelia de Lange syndrome (CdLS) is a rare genetic disorder caused by autosomal dominant or X-linked mutations. The prevalence of CdLS is estimated to be 1:10,000-30,000 newborns, but it is probably underestimated because milder cases may not be diagnosed. This syndrome is characterized by slow growth before and after birth with intellectual disability and short stature, major malformations such as facial anomalies, neurological disorders, and gastrointestinal and musculoskeletal malformations. Peculiar facial anomalies include arched and fused eyebrows on the midline, long eyelashes, anteverted nostrils, a mouth with downturned corners, and a very thin upper lip. To date, only medical and surgical therapeutic interventions to improve quality of life are recommended for these patients. No pharmacological therapy is validated for cognitive/behavioral disorders. Approximately 80% of patients with CdLS have mutations in one of the following 5 genes: NIPBL (60%), SMC1A, SMC3, RAD21 and HDAC8. These genes encode structural or accessory proteins of the cohesin complex. The cohesin complex is a multimeric system, highly conserved throughout cellular evolution from the most primitive life forms to human cells. Cohesins are essential elements for the structural maintenance of chromosomes (SMC) and interact with chromatin modulating its organization. Cohesins mediate the segregation of sister chromatids and play a fundamental role in the control of gene expression. A signaling pathway involved in all steps of central nervous system (CNS) development is the WNT pathway. Some of our previous studies have shown that an alteration of CNS development is related to a defect in the canonical WNT pathway. Current evidence suggests that CdLS malformations result from downregulation of molecular pathways during embryonic development and, in this context, our and previous studies have demonstrated that the canonical WNT pathway is perturbed. WNT has also recently been shown to play a key role in the functions of the cohesin complex in CdLS models and patient-derived fibroblasts. Our studies have highlighted how inhibition or loss of function of cohesins in in vivo models of CdLS affects CNS development. The WNT signaling pathway is involved in numerous events in the development and maintenance of adult tissue homeostasis by regulating cell proliferation, differentiation (including stem cell proliferation), migration, genetic stability and apoptosis, as well as in maintaining adult stem cells in a pluripotent state. LiCl-dependent activation of the WNT pathway is able to rescue the affected phenotype in CdLS models. Lithium is already widely used in psychiatry and has a long history of clinical efficacy as the first drug used in the treatment of mental illness. This drug is approved for the treatment of bipolar disorder because of its ability to stabilize mania and depression. Its use must be properly monitored so that ideal blood concentrations are maintained (0.4-1.2 mEq/L) and to monitor possible side effects. Recently, some studies have evaluated the effect of lithium in patients with features common to CdLS. A clinical trial proposed lithium therapy for the treatment of Fragile X Syndrome showing promising results. These patients exhibit traits similar to those of CdLS patients, particularly intellectual disabilities and autism spectrum disorders. Another study demonstrated the efficacy of lithium treatment as a mood stabilizer in two patients with SHANK3 gene mutations who were diagnosed with autism spectrum disorder in childhood. The project the investigators present aims to transfer the preliminary data obtained from in vitro and in vivo studies to patients with CdLS.
Due to the currently untreatable nature of the syndrome, this treatment could represent a potential therapeutic strategy aimed at improving the behavioral and intellectual disabilities commonly associated with CdLS.
Study Design the investigators designed a 52-week prospective treatment study to evaluate the efficacy of lithium carbonate in CdLS
Study Centers and Number of Subjects The investigators plan to enroll at least 34 subjects with CdLS, affiliated with the Child and Adolescent Neuropsychiatry Unit of the ASST Grande Ospedale Metropolitano Niguarda in Milan, the Pediatrics Unit of the ASST Lariana and the Child and Adolescent Neuropsychiatry Operating Unit (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico in Milan. Laboratory analyses for monitoring pharmacological treatment will be performed at the laboratories of the ASSTs involved in the study according to clinical practice. Monitoring of lipid peroxidation levels for research purposes will be performed in the Applied Biology laboratories at the Department of Health Sciences, University of Milan, with funding from Prof. Valentina Massa.
Patient recruitment Subjects who meet the defined inclusion and exclusion criteria will be recruited, after signing the informed consent, at the Child and Adolescent Neuropsychiatry Unit of the ASST Grande Ospedale Metropolitano Niguarda in Milan, the Pediatrics Unit of the ASST Lariana and the Child and Adolescent Neuropsychiatry Unit (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico in Milan.
Participants will receive an information document about the study and a consent form for the collection of biological material. They will also be given a telephone number and an email address to contact if they would like more information or wish to withdraw from the study for any reason.
Patients will attend the outpatient clinics of the Department of Childhood and Adolescent Neuropsychiatry (UONPIA) at the IRCSS Ca' Granda Foundation Ospedale Maggiore Policlinico in Milan for the initial NPI evaluation (T0). During the intervention period, monitoring visits will take place at the Childhood and Adolescent Neuropsychiatry unit of ASST Grande Ospedale Metropolitano Niguarda in Milan and the Pediatrics Unit of ASST Lariana at the following time points: T1, T2, T3, T4, T5, and T6.
At the end of the intervention period, participants will return to the UONPIA at the IRCSS Ca' Granda Foundation Ospedale Maggiore Policlinico of Milan (T7) to ensure continuity of care by a dedicated team of experts.
Methods The study drug, administered at a dosage of 10 mg/kg twice daily (150 mg or 300 mg lithium carbonate tablets), will be given to patients with an interval of 12 hours between doses. This proposed dosing regimen is based on previous experiences with lithium carbonate in pediatric patients. For patients who are unable to swallow capsules, the investigational medicinal product (IMP) can be provided as a solution.
The caregiver will record the date, time, and number of capsules administered on the Case Report Form (CRF). Symptoms of treatment intolerance include nausea, vomiting, diarrhea, hand tremors, fatigue, and muscle weakness. If any intolerance occurs during the study, the investigator may reduce the patient's dose, implement a single dose interruption, or switch to alternate day dosing. Patients who cannot tolerate the treatment even after a dose interruption must be withdrawn from the study.
The tapering process for treatment will involve a gradual reduction of the dosage, halving the dose every three days until complete cessation. The following medications are prohibited before and during the study:
- Concomitant antidepressants (such as venlafaxine and tricyclic antidepressants)
- Antipsychotics (including clozapine, haloperidol, phenothiazines, and risperidone)
- Antiepileptics (like carbamazepine, phenytoin, and phenobarbital)
- ACE inhibitors
- Amiodarone
- Calcium channel blockers
- Diuretics (such as thiazides and acetazolamide)
- Metronidazole
- Aminophylline
- Mannitol
Responsibilities In accordance with ICH and FDA requirements, the Investigator must always be able to account for all study drugs supplied. At the end of the study, it must be possible to reconcile the delivery records with the usage and returns records. Any discrepancies must be accounted for. Under no circumstances may the Investigator use study drugs other than those indicated in the protocol. Data collection and analysis The study will include the following phases: - Screening / Baseline (T0): subjects will be considered for the study if they meet the inclusion criteria. This phase includes: anamnesis, including drug history in treated patients and assessment of concomitant medications, and clinical assessment. Each subject will undergo cognitive assessment (Leiter-R scale and Vineland Adaptive Behavior Scales 2), behavioral scales (ABC and CARS-T) communication and social functioning scales (SCQ), sleep quality scales (SDSC) and quality of life (PedsQL) in collaboration with Dr. Ajmone of the U.O. of Childhood and Adolescent Neuropsychiatry (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico di Milano. Laboratory tests (hematology, biochemistry, urinalysis, serum pregnancy test for post-pubertal females and thyroid function tests) and 12-lead ECG will be performed. In the UNIMI Applied Biology laboratory, plasma levels of TBARS, known to be associated with lithium treatment, will be assessed. Written informed consent will be collected from parents/legal representatives of eligible CdLS patients willing to participate in the study. - Start Drug Treatment (SDT, 1 week after T0): Patients included in the study start taking the drug after clinical evaluation of the tests performed at T0. Blood sampling will be performed to prepare patient-derived lymphoblastoid lines by immortalizing lymphocytes with Epstein-Barr virus (EBV) at the "Istituto Giannina Gaslini" in Genoa and the mutation of the immortalized cell lines will be confirmed using molecular genetic techniques such as PCR and Sanger sequencing at the Medical Genetics laboratory of the University of Milan. The preparation of the lines guarantees genetically characterized material on which to perform molecular and cytotoxicity assays.
- T1 (2 weeks ± 3 days after SDT): clinical evaluation, laboratory tests including serum lithium levels, thyroid and renal function and ECG. Any adverse events will be recorded and concomitant medications will be evaluated.
- T2 (2 weeks ± 3 days after T1): clinical evaluation, blood tests including serum lithium levels, thyroid and renal function and ECG, as well as safety issues.
- T3 (1 month ± 1 week after T2): Clinical evaluation, laboratory tests (hematology, biochemistry, urinalysis, serum pregnancy test for post-pubertal females, and thyroid function test), and ECG. Plasma TBARS levels will be assessed.
- T4 (1 month ± 1 week after T3): Clinical evaluation, blood tests including serum lithium level, thyroid and renal function, and ECG, as well as safety concerns.
- T5 (3 months ± 1 week after T4): Laboratory tests (hematology, biochemistry, serum lithium level, urinalysis, serum pregnancy test for post-pubertal females, and thyroid function test), and 12-lead ECG will be performed. Plasma TBARS levels will be assessed.
- T6 (3 months ± 1 week after T5) ) - end of the first study period: Laboratory tests (hematology, biochemistry, serum lithium level, urinalysis, serum pregnancy test for post-pubertal females and thyroid function tests) and 12-lead ECG will be performed. Plasma TBARS levels will be assessed.
- Follow-up T7 (3 months ± 1 week after T6): All patients will return for final assessments. A final safety level (laboratory tests, ECG, vital signs) and efficacy assessment will be performed. Baseline scales and tests will be repeated.
Patients who benefit from lithium therapy will be guaranteed continuation of treatment and related drug tolerability/safety checks. Other analyses are part of clinical practice for managing CdLS patients.
Sample size The study plan to enroll 34 patients. The sample size was calculated using the Wilcoxon test considering as a null hypothesis that there are no differences in the primary outcome parameter (ABC scale) following treatment and as an alternative hypothesis that following treatment the ABC-c value decreases by 16 points (as per clinical trial on the efficacy of lithium in patients with fragile X18) and taking into account a 10% drop out.
- Conditions
- Cornelia De Lange Syndrome
- Being tested
- Lithium Carbonate Capsule
- Keywords
- Lithium treatment
- Medical subject headings
- De Lange Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Lithium Carbonate CapsuleDrug
10mg/Kg twice a day, 150mg or 300mg Lithium Carbonate
| Study group | Role | What they receive |
|---|---|---|
| CdLS patients with NIPBL mutation | Experimental | Patients will be given 10mg/Kg twice a day, 150mg or 300mg Lithium Carbonate Receives: Drug: Lithium Carbonate Capsule |
What is being measured
The primary outcome is the main question the study is designed to answer.
Behaviour
Behaviour assessed through the Aberrant Behaviour checklist (ABC1 scale) which mesaure psychiatric symptomatology and behavioral disorders also in patients with intellectual disabilities. minimum total score: 0; maximum total score:174. Higher scores mean worse outcome
Measured: Change at 12 months from baseline of supplementation
Secondary outcomes (7)
Communication
Social Communication Questionnaire questionnaire (SCQ; Rutter, Bailey\&Lord, 20032) to assess communication skills and social functioning; minimum score: 0; maximum score:40. Higher score means worse outcome.
Measured: Change at 12 months from baseline of supplementation
Behaviour
Childhood Autism Rating Scale (CARS 2 -T3) to assess autistic behaviors. minimum score: 15; maximum score:60. Higher score means worse outcome. Furthermore, for very serious patients, for whom a direct assessment with the Leiter could be insignificant or impossible, it would allow for the adaptation quotient (QD).
Measured: Change at 12 months from baseline of supplementation
Sleep disturbances
Sleep quality through the Sleep disturbances scale for children (SDSC5), to be administered to parents; there are two versions, one for subjects between 6-16 years, the other for children 3-6 years. minimum total score: 26; maximum total score:130. Higher scores mean worse outcome.
Measured: Change at 12 months from baseline of supplementation
Clinical features
Impression of change Clinical Global Impression of Change (CGI-C) filled out by the clinician at each visit. minimum total score:0; maximum total score:30. Higher scores mean worse outcome.
Measured: Change at 12 months from baseline of supplementation
Cognitive Performance
Cognitive Performance through the Leiter scale (Leiter-R, Roid \& Miller, 19974), a non-verbal scale that can be used for subjects between 2 and 20 years old. We use only cognitive battery and administer only the 4 mandatory subtests:
Total raw score: minimum 0, maximum 152
Measured: Change at 12 months from baseline of supplementation
Adaptive functioning in the different areas
Vineland Adaptive Behavior Scale 2 in order to also assess adaptive functioning in the different areas (motor, communication, autonomy, socialization). minimum total score: 0; maximum total score:766. Higher scores mean better outcome
Measured: Change at 12 months from baseline of supplementation
Quality of life
Improvement in quality of life through Pediatric Quality of Life Inventory (PedsQL6). minimum total score: 0; maximum total score:92. Higher scores mean worse outcome
Measured: Change at 12 months from baseline of supplementation
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jan 2025
- Study start1 May 2024
- Primary completionSep 2025 (estimated)
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cornelia De Lange 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 2/3
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 34 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Milan
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Aglaia Vignoli, University of Milan
- Investigators
- Aglaia Vignoli, Professor, MD, Principal investigator, University of Milan
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06789783
- Sponsor's protocol ID
- 210-18042023
- Other IDs
- patients association
- Acronym
- CLoSER
- Status last verified
- Nov 2024
- First submitted
- 19 Dec 2024
- Last updated
- 28 Jan 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Grazioli P, Parodi C, Mariani M, Bottai D, Di Fede E, Zulueta A, Avagliano L, Cereda A, Tenconi R, Wierzba J, Adami R, Iascone M, Ajmone PF, Vaccari T, Gervasini C, Selicorni A, Massa V. Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome. Cell Death Discov. 2021 Feb 17;7(1):34. doi: 10.1038/s41420-021-00414-2.
PubMed 33597506
Study at a glance
From the registry record, last updated by the sponsor on 28 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment
- ClinicalTrials.gov ID
- NCT06789783
- Acronym / sponsor ID
- CLoSER / 210-18042023
- Conditions
- Cornelia De Lange Syndrome
- Keywords
- Lithium treatment
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 34 participants (estimated)
- Lead sponsor
- University of MilanUniversity, hospital or other
- Study start
- 1 May 2024 (actual)
- Primary completion
- Sep 2025 (estimated)
- Study completion
- Dec 2026 (estimated)
- First posted
- 23 Jan 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 study "Cornelia de Lange Syndrome: assessing positive effects of Lithium treatment - CLoSER" aims to evaluate the effectiveness on behavioral modifications of lithium carbonate therapy in patients with Cornelia de Lange syndrome (CdLS).
CdLS is a rare genetic disease caused by autosomal mutations dominant or X-linked. The prevalence of CdLS is estimated to be between 1:10,000-30,000 newborns, but it is probably underestimated because the most cases mild ones may go undiagnosed. This syndrome is characterized by slow growth before and after birth with intellectual disability and short stature, from major malformations such as facial anomalies, neurological disorders, gastrointestinal and musculoskeletal malformations. To date, for these patients only targeted medical and surgical therapeutic interventions are recommended for improving the quality of life. No drug therapy is validated for the cognitive/behavioral disorders. It has been shown that lihium-dependent activation of the WNT pathway is able to recover the Abnormal phenotype in many CdLS models. Lithium is already widely used in psychiatry and has a long history of clinical efficacy.
Recently some studies are evaluating the effect of lithium in patients with characteristics common to CdLS showing promising results . This trial intends to transfer the preliminary data obtained from in vitro and in vivo studies on patients with CdLS.
Given the currently untreatable nature of the syndrome, this treatment could represent a possible therapeutic strategy aimed at improving the behavioral and intellectual disabilities typical of CdLS.
Detailed description
Research Objectives This study aims to evaluate the effectiveness of lithium carbonate therapy on behavioral changes in patients with Cornelia de Lange syndrome (CdLS). This is a multicenter and non-commercial pilot clinical study.
The specific objectives are the following:
PRIMARY OUTCOME - Improvement in the following parameters:
- Behavior assessed by Aberrant Behavior Checklist (ABC scale1), which measures psychiatric symptoms and behavioral disorders also in patients with intellectual disability;
SECONDARY OUTCOMES - Improvement in the following parameters:
- SCQ questionnaire (SCQ; Rutter, Bailey\&Lord, 20032) to assess communication skills and social functioning;
- Childhood Autism Rating Scale (CARS 2 -T3) to assess autistic behaviors;
- Cognitive Performance through the Leiter scale (Leiter-R, Roid \& Miller, 19974), a non-verbal scale that can be used for subjects between 2 and 20 years old.
- Vineland Adaptive Behavior Scales 2 to evaluate adaptive functioning in the different areas (motor, communication, autonomy, socialization). For severe patients, where a direct evaluation with the Leiter may be insignificant or impossible to conduct, it would provide an adaptation quotient (AQ).
- Sleep quality through the Sleep Disturbances Scale for children (SDSC5), to be administered to parents; there are two versions, one for subjects between 6 and 16 years old, the other for children 3-6 years old;
- Impression of Change Clinical Global Impression of Change (CGI-C) completed by the clinician at each visit;
- Improvement in quality of life through Pediatric Quality of Life Inventory (PedsQL6)
- Specific biomarkers will be used to measure lipid peroxidation in cell extracts, tissues and biological fluids.
Background Cornelia de Lange syndrome (CdLS) is a rare genetic disorder caused by autosomal dominant or X-linked mutations. The prevalence of CdLS is estimated to be 1:10,000-30,000 newborns, but it is probably underestimated because milder cases may not be diagnosed. This syndrome is characterized by slow growth before and after birth with intellectual disability and short stature, major malformations such as facial anomalies, neurological disorders, and gastrointestinal and musculoskeletal malformations. Peculiar facial anomalies include arched and fused eyebrows on the midline, long eyelashes, anteverted nostrils, a mouth with downturned corners, and a very thin upper lip. To date, only medical and surgical therapeutic interventions to improve quality of life are recommended for these patients. No pharmacological therapy is validated for cognitive/behavioral disorders. Approximately 80% of patients with CdLS have mutations in one of the following 5 genes: NIPBL (60%), SMC1A, SMC3, RAD21 and HDAC8. These genes encode structural or accessory proteins of the cohesin complex. The cohesin complex is a multimeric system, highly conserved throughout cellular evolution from the most primitive life forms to human cells. Cohesins are essential elements for the structural maintenance of chromosomes (SMC) and interact with chromatin modulating its organization. Cohesins mediate the segregation of sister chromatids and play a fundamental role in the control of gene expression. A signaling pathway involved in all steps of central nervous system (CNS) development is the WNT pathway. Some of our previous studies have shown that an alteration of CNS development is related to a defect in the canonical WNT pathway. Current evidence suggests that CdLS malformations result from downregulation of molecular pathways during embryonic development and, in this context, our and previous studies have demonstrated that the canonical WNT pathway is perturbed. WNT has also recently been shown to play a key role in the functions of the cohesin complex in CdLS models and patient-derived fibroblasts. Our studies have highlighted how inhibition or loss of function of cohesins in in vivo models of CdLS affects CNS development. The WNT signaling pathway is involved in numerous events in the development and maintenance of adult tissue homeostasis by regulating cell proliferation, differentiation (including stem cell proliferation), migration, genetic stability and apoptosis, as well as in maintaining adult stem cells in a pluripotent state. LiCl-dependent activation of the WNT pathway is able to rescue the affected phenotype in CdLS models. Lithium is already widely used in psychiatry and has a long history of clinical efficacy as the first drug used in the treatment of mental illness. This drug is approved for the treatment of bipolar disorder because of its ability to stabilize mania and depression. Its use must be properly monitored so that ideal blood concentrations are maintained (0.4-1.2 mEq/L) and to monitor possible side effects. Recently, some studies have evaluated the effect of lithium in patients with features common to CdLS. A clinical trial proposed lithium therapy for the treatment of Fragile X Syndrome showing promising results. These patients exhibit traits similar to those of CdLS patients, particularly intellectual disabilities and autism spectrum disorders. Another study demonstrated the efficacy of lithium treatment as a mood stabilizer in two patients with SHANK3 gene mutations who were diagnosed with autism spectrum disorder in childhood. The project the investigators present aims to transfer the preliminary data obtained from in vitro and in vivo studies to patients with CdLS.
Due to the currently untreatable nature of the syndrome, this treatment could represent a potential therapeutic strategy aimed at improving the behavioral and intellectual disabilities commonly associated with CdLS.
Study Design the investigators designed a 52-week prospective treatment study to evaluate the efficacy of lithium carbonate in CdLS
Study Centers and Number of Subjects The investigators plan to enroll at least 34 subjects with CdLS, affiliated with the Child and Adolescent Neuropsychiatry Unit of the ASST Grande Ospedale Metropolitano Niguarda in Milan, the Pediatrics Unit of the ASST Lariana and the Child and Adolescent Neuropsychiatry Operating Unit (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico in Milan. Laboratory analyses for monitoring pharmacological treatment will be performed at the laboratories of the ASSTs involved in the study according to clinical practice. Monitoring of lipid peroxidation levels for research purposes will be performed in the Applied Biology laboratories at the Department of Health Sciences, University of Milan, with funding from Prof. Valentina Massa.
Patient recruitment Subjects who meet the defined inclusion and exclusion criteria will be recruited, after signing the informed consent, at the Child and Adolescent Neuropsychiatry Unit of the ASST Grande Ospedale Metropolitano Niguarda in Milan, the Pediatrics Unit of the ASST Lariana and the Child and Adolescent Neuropsychiatry Unit (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico in Milan.
Participants will receive an information document about the study and a consent form for the collection of biological material. They will also be given a telephone number and an email address to contact if they would like more information or wish to withdraw from the study for any reason.
Patients will attend the outpatient clinics of the Department of Childhood and Adolescent Neuropsychiatry (UONPIA) at the IRCSS Ca' Granda Foundation Ospedale Maggiore Policlinico in Milan for the initial NPI evaluation (T0). During the intervention period, monitoring visits will take place at the Childhood and Adolescent Neuropsychiatry unit of ASST Grande Ospedale Metropolitano Niguarda in Milan and the Pediatrics Unit of ASST Lariana at the following time points: T1, T2, T3, T4, T5, and T6.
At the end of the intervention period, participants will return to the UONPIA at the IRCSS Ca' Granda Foundation Ospedale Maggiore Policlinico of Milan (T7) to ensure continuity of care by a dedicated team of experts.
Methods The study drug, administered at a dosage of 10 mg/kg twice daily (150 mg or 300 mg lithium carbonate tablets), will be given to patients with an interval of 12 hours between doses. This proposed dosing regimen is based on previous experiences with lithium carbonate in pediatric patients. For patients who are unable to swallow capsules, the investigational medicinal product (IMP) can be provided as a solution.
The caregiver will record the date, time, and number of capsules administered on the Case Report Form (CRF). Symptoms of treatment intolerance include nausea, vomiting, diarrhea, hand tremors, fatigue, and muscle weakness. If any intolerance occurs during the study, the investigator may reduce the patient's dose, implement a single dose interruption, or switch to alternate day dosing. Patients who cannot tolerate the treatment even after a dose interruption must be withdrawn from the study.
The tapering process for treatment will involve a gradual reduction of the dosage, halving the dose every three days until complete cessation. The following medications are prohibited before and during the study:
- Concomitant antidepressants (such as venlafaxine and tricyclic antidepressants)
- Antipsychotics (including clozapine, haloperidol, phenothiazines, and risperidone)
- Antiepileptics (like carbamazepine, phenytoin, and phenobarbital)
- ACE inhibitors
- Amiodarone
- Calcium channel blockers
- Diuretics (such as thiazides and acetazolamide)
- Metronidazole
- Aminophylline
- Mannitol
Responsibilities In accordance with ICH and FDA requirements, the Investigator must always be able to account for all study drugs supplied. At the end of the study, it must be possible to reconcile the delivery records with the usage and returns records. Any discrepancies must be accounted for. Under no circumstances may the Investigator use study drugs other than those indicated in the protocol. Data collection and analysis The study will include the following phases: - Screening / Baseline (T0): subjects will be considered for the study if they meet the inclusion criteria. This phase includes: anamnesis, including drug history in treated patients and assessment of concomitant medications, and clinical assessment. Each subject will undergo cognitive assessment (Leiter-R scale and Vineland Adaptive Behavior Scales 2), behavioral scales (ABC and CARS-T) communication and social functioning scales (SCQ), sleep quality scales (SDSC) and quality of life (PedsQL) in collaboration with Dr. Ajmone of the U.O. of Childhood and Adolescent Neuropsychiatry (UONPIA) Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico di Milano. Laboratory tests (hematology, biochemistry, urinalysis, serum pregnancy test for post-pubertal females and thyroid function tests) and 12-lead ECG will be performed. In the UNIMI Applied Biology laboratory, plasma levels of TBARS, known to be associated with lithium treatment, will be assessed. Written informed consent will be collected from parents/legal representatives of eligible CdLS patients willing to participate in the study. - Start Drug Treatment (SDT, 1 week after T0): Patients included in the study start taking the drug after clinical evaluation of the tests performed at T0. Blood sampling will be performed to prepare patient-derived lymphoblastoid lines by immortalizing lymphocytes with Epstein-Barr virus (EBV) at the "Istituto Giannina Gaslini" in Genoa and the mutation of the immortalized cell lines will be confirmed using molecular genetic techniques such as PCR and Sanger sequencing at the Medical Genetics laboratory of the University of Milan. The preparation of the lines guarantees genetically characterized material on which to perform molecular and cytotoxicity assays.
- T1 (2 weeks ± 3 days after SDT): clinical evaluation, laboratory tests including serum lithium levels, thyroid and renal function and ECG. Any adverse events will be recorded and concomitant medications will be evaluated.
- T2 (2 weeks ± 3 days after T1): clinical evaluation, blood tests including serum lithium levels, thyroid and renal function and ECG, as well as safety issues.
- T3 (1 month ± 1 week after T2): Clinical evaluation, laboratory tests (hematology, biochemistry, urinalysis, serum pregnancy test for post-pubertal females, and thyroid function test), and ECG. Plasma TBARS levels will be assessed.
- T4 (1 month ± 1 week after T3): Clinical evaluation, blood tests including serum lithium level, thyroid and renal function, and ECG, as well as safety concerns.
- T5 (3 months ± 1 week after T4): Laboratory tests (hematology, biochemistry, serum lithium level, urinalysis, serum pregnancy test for post-pubertal females, and thyroid function test), and 12-lead ECG will be performed. Plasma TBARS levels will be assessed.
- T6 (3 months ± 1 week after T5) ) - end of the first study period: Laboratory tests (hematology, biochemistry, serum lithium level, urinalysis, serum pregnancy test for post-pubertal females and thyroid function tests) and 12-lead ECG will be performed. Plasma TBARS levels will be assessed.
- Follow-up T7 (3 months ± 1 week after T6): All patients will return for final assessments. A final safety level (laboratory tests, ECG, vital signs) and efficacy assessment will be performed. Baseline scales and tests will be repeated.
Patients who benefit from lithium therapy will be guaranteed continuation of treatment and related drug tolerability/safety checks. Other analyses are part of clinical practice for managing CdLS patients.
Sample size The study plan to enroll 34 patients. The sample size was calculated using the Wilcoxon test considering as a null hypothesis that there are no differences in the primary outcome parameter (ABC scale) following treatment and as an alternative hypothesis that following treatment the ABC-c value decreases by 16 points (as per clinical trial on the efficacy of lithium in patients with fragile X18) and taking into account a 10% drop out.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| CdLS patients with NIPBL mutation | Experimental | Drug: Lithium Carbonate CapsulePatients will be given 10mg/Kg twice a day, 150mg or 300mg Lithium Carbonate |
Who may qualify
- Ages
- 4 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (7 listed)
- Age > 4 years
- Body weight within the normal range in the reference range for CdLS, based on age and height
- Diagnosis of CdLS based on consensus clinical criteria and a confirmed mutation in the NIPBL gene
- Stable drug regimen for 4 weeks prior to starting the study
- Written consent signed by parent/legal guardian/representative prior to the screening visit
Key exclusion criteria (4 listed)
- The patient is participating in another clinical trial
- QT interval prolongation, thyroid dysfunction, renal insufficiency, hepatic insufficiency, leukopenia, or other currently clinically significant medical disorders (as determined by the investigator), other than those directly related to CdLS
- QTcF interval on ECG greater than 450 msec
- Severe diabetes mellitus or inherited metabolic disorder
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 |
|---|---|---|
| Lithium Carbonate Capsule10mg/Kg twice a day, 150mg or 300mg Lithium Carbonate | Drug | CdLS patients with NIPBL mutation |
Primary outcome
Behaviour
Time frame: Change at 12 months from baseline of supplementation
Behaviour assessed through the Aberrant Behaviour checklist (ABC1 scale) which mesaure psychiatric symptomatology and behavioral disorders also in patients with intellectual disabilities. minimum total score: 0; maximum total score:174. Higher scores mean worse outcome
7 secondary outcomes
Communication
Time frame: Change at 12 months from baseline of supplementation
Behaviour
Time frame: Change at 12 months from baseline of supplementation
Sleep disturbances
Time frame: Change at 12 months from baseline of supplementation
Clinical features
Time frame: Change at 12 months from baseline of supplementation
Cognitive Performance
Time frame: Change at 12 months from baseline of supplementation
Adaptive functioning in the different areas
Time frame: Change at 12 months from baseline of supplementation
Quality of life
Time frame: Change at 12 months from baseline of supplementation
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 28 Jan 2025.
- Background: PubMed 33597506Grazioli P, Parodi C, Mariani M, Bottai D, Di Fede E, Zulueta A, Avagliano L, Cereda A, Tenconi R, Wierzba J, Adami R, Iascone M, Ajmone PF, Vaccari T, Gervasini C, Selicorni A, Massa V. Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome. Cell Death Discov. 2021 Feb 17;7(1):34. doi: 10.1038/s41420-021-00414-2.
- Individual participant dataSharing planned: No
Related trials for Cornelia De Lange Syndrome
RecruitingObservational study
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Rare Disorders, Undiagnosed Disorders
Not yet recruitingPhase 2
Use of N-Acetylcysteine in the Treatment of Repetitive and Self-Injurious Behaviors in Cornelia de Lange Syndrome
Cornelia de Lange Syndrome
Recruiting
Behavioral Assessment and Treatment of Problem Behavior in Children With Cornelia de Lange Syndrome
Cornelia de Lange Syndrome
RecruitingObservational study
GROWing Up With Rare GENEtic Syndromes
Prader-Willi Syndrome, PWS-like Syndrome
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.
Aglaia Vignoli, Professor, MD principal investigator
University of Milan
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing Lithium Carbonate Capsule in people with Cornelia De Lange Syndrome, run by University of Milan 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 7 inclusion and 4 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 28 Jan 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.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
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 Aglaia Vignoli, Professor, MD (+390264443960, aglaia.vignoli@unimi.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Behaviour (time frame: Change at 12 months from baseline of supplementation). 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 NCT06789783, which also lists 1 linked publication.
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 28 Jan 2025.