Clinical trial

Improvement of Synaptic Plasticity and Cognitive Function in RAS Pathway Disorders

Name
SYN-1748-MAL-0030-I
Description
The project is targeting cognitive impairment, one of the main health problems of patients with RAS pathway disorders. The aim of this study is to translate findings of animal studies to humans. This has been done by the applicants successfully for Lovastatin in Nf1. This result will be transferred to patients with Noonan Syndrome. lamotrigine is most likely a more effective and promising substance improving synaptic plasticity and consecutive cognitive function. It is expected that both substances are improving synaptic plasticity as well as alertness and changes in alertness may be a precondition for improvement of cognition.
Trial arms
Trial start
2019-03-22
Estimated PCD
2023-02-09
Trial end
2023-10-31
Status
Terminated
Phase
Early phase I
Treatment
Lovastatin
oral application prior to transcranial magnetic stimulation intervention
Arms:
Exp. I: Noonan Syndrome - Lovastatin
Lamotrigine
oral application prior to transcranial magnetic stimulation intervention
Arms:
Exp. II: Noonan Syndrome - Lamotrigine, Exp. III: Neurofibromatosis Type 1 - Lamotrigine
Size
16
Primary endpoint
Long-term potentiation (LTP)-like plasticity measured with transcranial magnetic stimulation (TMS)
12 months
Eligibility criteria
Inclusion Criteria: 1. Group 1: NS, Group 2: NF1 (both genetically assured) 2. Age ≥16 years 3. The adolescent (≥16) and legal guardian who are capable to give their consent and understand the aim and rationale of the study. In case of doubts, an independent medical practitioner will evaluate the capacity to consent. 4. Signed informed consent if ≥ 16 years and legal guardian. 5. Persons who are ≥ 18 years old and capable to give their consent and understand the aim and rationale of the study. In case of doubts, an independent medical practitioner will evaluate the capacity to consent. 6. Signed informed consent if ≥ 18 years. 7. Male participants and female participants who are not capable of bearing children or who use a method of contraception that is medically approved by the health authority of the respective country. Exclusion Criteria: 1. Epilepsy 2. Medication with known CNS effects 3. Severe mental retardation 4. Side effects during previous medication with and contraindications for LTG and/or LOV and/or TMS 5. Psychiatric diseases 6. Previous history of allergic reactions with LTG and LOV medications 7. Potentially unreliable patients 8. Patients who are not suitable for the study in the opinion of the investigator 9. Pregnancy (incl. positive urine pregnancy test) 10. Persons who are incapable of giving consent or do not understand the aim or rationale of the study.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'CROSSOVER', 'interventionModelDescription': 'Monocenter, randomized, double-blind, parallel-group, placebo controlled, cross-over design with a series of three experiments (Noonan Syndrome: 2 experiments; Neurofibromatosis type 1 1 experiment) and n=14 participants per experiments', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 16, 'type': 'ACTUAL'}}
Updated at
2023-11-30

1 organization

2 products

2 indications

Product
Lovastatin