Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age4+
SponsorUniversity of Milan

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

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 design

Treatments tested in this trial

  • Lithium Carbonate Capsule

Treatment groups

34 Participants
are divided into 1 treatment group

Sponsors and collaborators