Could lithium ease symptoms of rare Autism-Linked condition?
NCT ID NCT06776848
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether lithium carbonate can improve behavior and thinking in people with a rare genetic disorder caused by changes in the TBR1 gene. Twelve participants aged 6 and older will take lithium for 24 months after a 6-12 month observation period. The goal is to see if the treatment is safe and helps with daily living skills.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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6 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Written informed consent from the patient, parent or legal representative * ≥6 years old at the time of consent * Proven pathogenic or probably pathogenic TBR1 variant (SNV confirmed by Sanger sequencing or CNV including only TBR1) * If applicable: Stable concomitant psychoactive medication regimen (dose and schedule) ≥2 months prior to lithium initiation * Affected individuals able to take tablet /capsules orally * Highly effective method of contraception in affected female individuals of childbearing age (Combined hormonal contraception, progestogen-only hormonal contraception, intrauterine device, intrauterine hormone-releasing system or abstinence) during treatment and for at least 3 months after the final dose of lithium * Highly effective method of contraception in affected men individuals of childbearing age (condom or abstinence) during the treatment and for at least 5 days after the final dose of lithium * 1 available parent/guardian able to attend all visits having acceptable reading skills Exclusion Criteria: Criteria related to associated pathologies leading to particular risks: * Renal/liver insufficiency (disturbed liver function, abnormal creatinine clearance) * Unbalanced thyroid or diabetic pathology * Long QT/Brugada syndrome or familial antecedent of Brugada syndrome, cardiac insufficiency * Addison disease, dehydration, sodium restriction * Non-stabilized epileptic disease. Criteria related to contra-indication to treatment: * Patient with concomitant diseases for which the experimental treatment by lithium could alter the tolerance * Hypersensitivity to lactose, lithium or one of its excipients * Patient with a wheat allergy (other than celiac disease) * Pregnant or breastfeeding woman Criteria related to treatments/procedures: * Parent/guardian incapable of expressing consent * Person not affiliated to a national health insurance scheme * Person subject to a court order * Cognitivo-behavioural therapy focused on ASD in 6 weeks previous to inclusion * Other genetic pathogenic variant associated to neurocognitive disorders * Any introduction of psychotropic molecules within 2 months prior to the trial, including neuroleptics, monoamine oxidase inhibitors, stimulants, antidepressants. * Concomitant use of Angiotensin-Converting Enzyme (ACE) inhibitor, angiotensin II receptor antagonists, Nonsteroidal anti-inflammatory drugs, diuretics. * Current lithium treatment * Severe behavioural disorder or refusal to take drug treatment not allowing for compliance with medication; * Impossibility to perform blood tests to check the lithiaemia when the patient is included. * Participation in another therapeutic trial
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU Dijon Bourgogne
RECRUITINGDijon, 21000, France