Evaluation of a Treatment With Allopurinol in Adenylosuccinate Lyase Deficiency (ADSL)
Primary Purpose
Adenylosuccinate Lyase Deficiency
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Allopurinol
Sponsored by
About this trial
This is an interventional treatment trial for Adenylosuccinate Lyase Deficiency focused on measuring Adenylosuccinate lyase, Deficit, Allopurinol, Autism, Epilepsy
Eligibility Criteria
Inclusion Criteria:
- Child (minimum age 18 months) or adult with adenylosuccinate lyase; deficiency (ADSL) confirmed by quantification of SAICAr and S-Ado urinary;
Girls / women of childbearing age must:
- have a negative pregnancy test;
- agree to use a reliable method of contraception from the baseline visit to the last dose of study treatment
- Consent of the patient, his parents or his legal representative;
- Beneficiary of social security (affiliated or entitled).
Exclusion Criteria:
- Refusal of the child, his parents or the patient or his representative;
- Allergy known to allopurinol or to one of the constituents of the product (lactose in particular);
- Patients treated with Antipurines (azathioprine, mercaptopurine);
- Patients treated with vidarabine, cytotoxic drugs (eg cyclophosphamide, doxorubicin, bleomycin, procarbazine, alkyl halides), ciclosporin, or didanosine
- Renal failure characterized by creatinine clearance <80 ml/mn
- Hepatic insufficiency
- Medullary insufficiency but possibly serious
- Breastfeeding
- Pregnancy or wishing to conceive during the study period
Sites / Locations
- LA PITIE-SALPETRIERE Hospital, AP-HP
- Department of Pediatry. Reference centre of Hereditary diseases of the metabolism of child and adult. Necker - Enfants malades Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Allopurinol
Arm Description
Oral administration of Allopurinol (Zyloric®) for 12 months without exceeding 400 mg / day in children and 900 mg / day in adults, with dosage adjustment in case of renal failure
Outcomes
Primary Outcome Measures
Measurement of adaptive functional improvement : composite total score for Vineland II adaptive behaviour Scale
to assess Efficacy of Allopurinol (Zyloric)® treatment from Baseline : For each scale : Mean : 100 SD : 15
Adaptive behaviour composite : Range 20 to 180 -Domains scores : Range 20 to 140 -Communication : Range 20 to 140 -Daily living skills : Range 20 to 140 -Socialization : 20 to 140 -Motor skills : 20 to 140 For each scale values are considered to be better or worse outcome :High 130 to 140 -Moderately High 115 to 129 -Adequate 86 to 114 -Moderately Low 71 to 85 -Low 20 to 70 Total score is obtained by summing the subdomains scores
Secondary Outcome Measures
Evolution of the Scores of different subdomains Vineland II scale from baseline
Clinical evolution for developmental and cognitive assessment
Evolution of the Psycho-Educative Profile (PEP III/R) from baseline
Clinical evolution for developmental and cognitive assessment
Evolution of the Score ADI-R (Autism Diagnostic Interview-Revised) from baseline
Clinical evaluation for autistic symptoms : scale ranges :
A : Social interactions: 0 to 30 (significative if >10)
B : Communication : 0 to 26 (significative if > 7 or 8)
C : Repetitive and restricted interests : 0 to 16 (significative if >3)
D : Developmental abnormality present before 36 months : 0 to 5 (significative if >1)
better score : 0 (non autistic) - worse score : the higher score is the worst
Evolution of the Score ADOS-2 (Autism Diagnostic Observation Schedule 2) from baseline
Clinical evaluation for autistic symptoms. Scale ranges :
A : Socialization : social interactions and communication : 0 to 20 (social interactions : 0 to 6 -communication : 0 to 14)
B : Restricted and repetitive interests : 0 to 8
Total : A+B : 0 to 28
Autism : total score>12 - Autism Spectrum Disorder : total score >8
Better score : 0 - Worse score : the highest score is the worst
Evolution of the Score on Conners hyperactivity Scale
Clinical evolution for behavioral disorders and adaptive functioning
Conners Scale for Parents :
- Subscales : Behavioural difficulties (items 2-8-14-19-20-27-35-39) : 0 to 24 Learning difficulties (items 10-25-31-37) : 0 to 12 Somatisation (items 32-41-43-44) : 0 to 12 Impulsivity, hyperactivity (items 4-5-11-13): 0 to 12 Anxiety (items 12-16-24-47): 0 to 12
-Hyperactivity index : sum of the items (4-7-11-13-14-25-31-33-37-38) divided by 10 : 0 to 3
Conners Scale for teachers :
- Subscales : Behavioural difficulties (items 4-5-6-10-11-12-23-27) : 0 to 24 Impulsivity, hyperactivity (items 1-2-3-8-14-15-16) : 0 to 21 Inattention, passivity (items 7-9-18-20-21-22-26-28) : 0 to 24
-Hyperactivity index (sum of the items 1-5-7-8-10-11-14-15-21-26 divided by 10) : 0 to 3
Better score : 0 - Worse score : the highest score is the worst -Hyperactivity index : Significative if> 1,5
Evolution of the Score on ABC scale (Aberrant Behaviour Checklist)
Clinical evolution for behavioral disorders and adaptive functioning scale ranges :
Irritability : 0 to 45
Lethargy : 0 to 48
Stereotypy : 0 to 21
Hyperactivity : 0 to 48
Inappropriate speech : 0 to 12
Better score : 0 -Worse score : the highest score is the worst on each scale- there is no total score
Evolution of SAICAr levels in the urine
Evolution of the quantity of urinary metabolites from Baseline
Evolution of S-Ado levels in the urine
Evolution of the quantity of urinary metabolites from Baseline
Evolution of SAICAr levels in the blood
Evolution of the quantity of plasma metabolites from Baseline
Evolution of S-Ado levels in the blood
Evolution of the quantity of plasma metabolites from Baseline
Evolution of the number of seizures from Baseline for epileptic patients
at baseline, performing neurological examinations and interrogation
Evolution of antiepileptic treatments from Baseline for epileptic patients
at baseline, performing neurological examinations and interrogation
Evolution of electroencephalogram tracing from Baseline for epileptic patients
normal/abnormal
Full Information
NCT ID
NCT03776656
First Posted
August 13, 2018
Last Updated
October 10, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
URC-CIC Paris Descartes Necker Cochin
1. Study Identification
Unique Protocol Identification Number
NCT03776656
Brief Title
Evaluation of a Treatment With Allopurinol in Adenylosuccinate Lyase Deficiency
Acronym
ADSL
Official Title
Evaluation of a Treatment With Allopurinol on Autistic Disorders and Epilepsy in Adenylosuccinate Lyase Deficiency (ADSL)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
October 14, 2019 (Actual)
Primary Completion Date
June 17, 2022 (Actual)
Study Completion Date
June 17, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
URC-CIC Paris Descartes Necker Cochin
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to evaluate the effectiveness of allopurinol treatment at 12 months on the adaptive and cognitive functioning of patients with adenylosuccinate lyase deficiency (ADSL). The psychiatric evaluation will involve the use of standardized tools prior to initiation of treatment, and will be repeated 6 months and 12 months after the start of treatment.
The decrease in the concentration of SAICAR and S-Ado metabolites, which are markers of adenylosuccinate lyase (ADSL) deficiency, will also be quantified.
Similarly, the efficacy of allopurinol on epileptic seizures for epileptic patients and on electrocardiogram abnormalities will be evaluated secondarily
Detailed Description
Adenylosuccinate lyase deficiency (ADSL) is a rare disorder of purine metabolism whose symptoms are mental retardation, autistic disorders, epilepsy, related to the accumulation of succinylpurines: succinylaminoimidazole carboxamide riboside (SAICAr) and succinyladenosine (S- Ado). The S-Ado / SAICAr ratio in the cerebrospinal fluid (CSF) is correlated with the clinical severity: the cerebral toxicity of SAICAr is incriminated. There is no specific treatment.
Based on the work of Gertrude B. Elion (1988 Nobel Prize in Medicine), who reports that allopurinol (a structural analogue of hypoxanthine) can be a substrate for hypoxanthine phosphoribosyltransferase (HPRT) and thus produce allopurinol ribonucleotides with as a first step in the de novo synthesis of purines, investigators tested the hypothesis that treatment with allopurinol in children with ADSL deficiency would reduce the production of the toxic metabolite SAICAr.
This hypothesis was validated in 3 minor patients with biological and clinical improvement.
So the investigators put the phase II, non-comparative study based on 4 visits to Necker-Enfants malades Hospital or La Pitié-Salpêtrière Hospital: Month 0 (before treatment), Month 3, Month 6 and Month 12 after the start of treatment.
After verification of the inclusion criteria and information of the parents or the patient or guardian, signature of the consent and inclusion of the patient:
Clinical and neurological evaluation;
Psychiatric assessment with standardized tests;
Biological evaluation: determination of urinary and plasma metabolites (SAICAr, S-Ado, ...) Experimental treatment: Allopurinol (Zyloric®) will be administered orally for 12 months without exceeding 400 mg / day in children and 900 mg / day in adults, with dosage adjustment in case of renal failure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adenylosuccinate Lyase Deficiency
Keywords
Adenylosuccinate lyase, Deficit, Allopurinol, Autism, Epilepsy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Allopurinol
Arm Type
Experimental
Arm Description
Oral administration of Allopurinol (Zyloric®) for 12 months without exceeding 400 mg / day in children and 900 mg / day in adults, with dosage adjustment in case of renal failure
Intervention Type
Drug
Intervention Name(s)
Allopurinol
Other Intervention Name(s)
Zyloric®
Intervention Description
Daily oral administration
Primary Outcome Measure Information:
Title
Measurement of adaptive functional improvement : composite total score for Vineland II adaptive behaviour Scale
Description
to assess Efficacy of Allopurinol (Zyloric)® treatment from Baseline : For each scale : Mean : 100 SD : 15
Adaptive behaviour composite : Range 20 to 180 -Domains scores : Range 20 to 140 -Communication : Range 20 to 140 -Daily living skills : Range 20 to 140 -Socialization : 20 to 140 -Motor skills : 20 to 140 For each scale values are considered to be better or worse outcome :High 130 to 140 -Moderately High 115 to 129 -Adequate 86 to 114 -Moderately Low 71 to 85 -Low 20 to 70 Total score is obtained by summing the subdomains scores
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Evolution of the Scores of different subdomains Vineland II scale from baseline
Description
Clinical evolution for developmental and cognitive assessment
Time Frame
at 0, 6 months and 12 months
Title
Evolution of the Psycho-Educative Profile (PEP III/R) from baseline
Description
Clinical evolution for developmental and cognitive assessment
Time Frame
at 0, 12 months
Title
Evolution of the Score ADI-R (Autism Diagnostic Interview-Revised) from baseline
Description
Clinical evaluation for autistic symptoms : scale ranges :
A : Social interactions: 0 to 30 (significative if >10)
B : Communication : 0 to 26 (significative if > 7 or 8)
C : Repetitive and restricted interests : 0 to 16 (significative if >3)
D : Developmental abnormality present before 36 months : 0 to 5 (significative if >1)
better score : 0 (non autistic) - worse score : the higher score is the worst
Time Frame
at 0, 12 months
Title
Evolution of the Score ADOS-2 (Autism Diagnostic Observation Schedule 2) from baseline
Description
Clinical evaluation for autistic symptoms. Scale ranges :
A : Socialization : social interactions and communication : 0 to 20 (social interactions : 0 to 6 -communication : 0 to 14)
B : Restricted and repetitive interests : 0 to 8
Total : A+B : 0 to 28
Autism : total score>12 - Autism Spectrum Disorder : total score >8
Better score : 0 - Worse score : the highest score is the worst
Time Frame
at 0, 12 months
Title
Evolution of the Score on Conners hyperactivity Scale
Description
Clinical evolution for behavioral disorders and adaptive functioning
Conners Scale for Parents :
- Subscales : Behavioural difficulties (items 2-8-14-19-20-27-35-39) : 0 to 24 Learning difficulties (items 10-25-31-37) : 0 to 12 Somatisation (items 32-41-43-44) : 0 to 12 Impulsivity, hyperactivity (items 4-5-11-13): 0 to 12 Anxiety (items 12-16-24-47): 0 to 12
-Hyperactivity index : sum of the items (4-7-11-13-14-25-31-33-37-38) divided by 10 : 0 to 3
Conners Scale for teachers :
- Subscales : Behavioural difficulties (items 4-5-6-10-11-12-23-27) : 0 to 24 Impulsivity, hyperactivity (items 1-2-3-8-14-15-16) : 0 to 21 Inattention, passivity (items 7-9-18-20-21-22-26-28) : 0 to 24
-Hyperactivity index (sum of the items 1-5-7-8-10-11-14-15-21-26 divided by 10) : 0 to 3
Better score : 0 - Worse score : the highest score is the worst -Hyperactivity index : Significative if> 1,5
Time Frame
at 0, 6 months and 12 months
Title
Evolution of the Score on ABC scale (Aberrant Behaviour Checklist)
Description
Clinical evolution for behavioral disorders and adaptive functioning scale ranges :
Irritability : 0 to 45
Lethargy : 0 to 48
Stereotypy : 0 to 21
Hyperactivity : 0 to 48
Inappropriate speech : 0 to 12
Better score : 0 -Worse score : the highest score is the worst on each scale- there is no total score
Time Frame
at 0, 6 months and 12 months
Title
Evolution of SAICAr levels in the urine
Description
Evolution of the quantity of urinary metabolites from Baseline
Time Frame
at 0, 6 months and 12 months
Title
Evolution of S-Ado levels in the urine
Description
Evolution of the quantity of urinary metabolites from Baseline
Time Frame
at 0, 6 months and 12 months
Title
Evolution of SAICAr levels in the blood
Description
Evolution of the quantity of plasma metabolites from Baseline
Time Frame
at 0, 6 months and 12 months
Title
Evolution of S-Ado levels in the blood
Description
Evolution of the quantity of plasma metabolites from Baseline
Time Frame
at 0, 6 months and 12 months
Title
Evolution of the number of seizures from Baseline for epileptic patients
Description
at baseline, performing neurological examinations and interrogation
Time Frame
at 0 and 12 months
Title
Evolution of antiepileptic treatments from Baseline for epileptic patients
Description
at baseline, performing neurological examinations and interrogation
Time Frame
at 0 and 12 months
Title
Evolution of electroencephalogram tracing from Baseline for epileptic patients
Description
normal/abnormal
Time Frame
at 0 and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Child (minimum age 18 months) or adult with adenylosuccinate lyase; deficiency (ADSL) confirmed by quantification of SAICAr and S-Ado urinary;
Girls / women of childbearing age must:
have a negative pregnancy test;
agree to use a reliable method of contraception from the baseline visit to the last dose of study treatment
Consent of the patient, his parents or his legal representative;
Beneficiary of social security (affiliated or entitled).
Exclusion Criteria:
Refusal of the child, his parents or the patient or his representative;
Allergy known to allopurinol or to one of the constituents of the product (lactose in particular);
Patients treated with Antipurines (azathioprine, mercaptopurine);
Patients treated with vidarabine, cytotoxic drugs (eg cyclophosphamide, doxorubicin, bleomycin, procarbazine, alkyl halides), ciclosporin, or didanosine
Renal failure characterized by creatinine clearance <80 ml/mn
Hepatic insufficiency
Medullary insufficiency but possibly serious
Breastfeeding
Pregnancy or wishing to conceive during the study period
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pascale De LONLAY, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Irène CEBALLOS-PICOT, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Laurence ROBEL-GALLI, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
Facility Information:
Facility Name
LA PITIE-SALPETRIERE Hospital, AP-HP
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Department of Pediatry. Reference centre of Hereditary diseases of the metabolism of child and adult. Necker - Enfants malades Hospital
City
Paris
ZIP/Postal Code
75015
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Evaluation of a Treatment With Allopurinol in Adenylosuccinate Lyase Deficiency
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