A Cohort of Patients With Cystinosis : Compliance to Cysteamine and Neurological Complications

Cystinosis Clinical Trial

— Crystobs  

Official title:

A Cohort of Patients With Cystinosis : Compliance to Cysteamine and Neurological Complications

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02012114
• Other study ID #: 2010-605
• Status: Completed
• Phase: N/A
• Start date: December 2011
• Est. completion date: December 14, 2021

Study information

• Verified date: May 2022
• Source: Hospices Civils de Lyon
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Preventing late onset of Cystinosis such as neurological complications and improving compliance to cysteamine treatment remain major challenges in management of subjects with cystinosis.

This study is designed to describe the relationship between compliance of patients with cystinosis treated with cysteamine and treatment efficacy and to understand the pathophysiologic mechanism of neurological disorders. Is cysteamine crossing the blood brain barrier? What is the impact of cystine accumulation in Cerebro Spinal Fluid and Central Nervous System? Our Primary objective is to study the relationship between compliance of patients treated with cysteamine and the WBC cystine level.

Secondary, the study will assess relationship between compliance to cysteamine and its neurological consequences.

The expected duration of the study is 48 months. The enrolment period is 24 months and the study participation of each subject is 24 months. Eligible participants are male and female (age > 4 years) with confirmed diagnosis of cystinosis and receiving any oral cysteamine treatment: Cystagon or RP103.

The compliance under cysteamine is measured using electronic devices, accountability of study treatment, and information in patients' diary. Specific memory and visuoperceptual tests are performed at the beginning and at the end of patients'participation. Nuclear Magnetic Resonance spectroscopy is used to detect possible sites of cystine accumulation in the CNS and their relationship with compliance to cysteamine treatment. NMRS is also used to establish a relationship with the neuropsychological status of the subject.

To describe absorption, distribution and elimination of cysteamine, and its metabolic pathways, and to determine the concentration effect and dose effect relationship, blood samples are performed at each study visit. A lumbar puncture is also proposed to participants to verify if cysteamine is crossing the blood brain barrier. New tools are used to compare metabonomic networks in patients with cystinosis and their controls.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 65
• Est. completion date: December 14, 2021
• Est. primary completion date: December 5, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 4 Years and older

Eligibility

• Male and female subjects with confirmed diagnosis of nephropathic cystinosis (defined by clinical signs and WBC cystine level).

• Age > 4 years.

• Subjects receiving any oral cysteamine treatment: Cystagon or RP103.

• Sexually active female subjects of childbearing potential must agree to utilize the same acceptable form of contraception from day 1 through completion of the study.

• Subjects or their parent or legal guardian must provide written informed consent prior to participation in the study.

• Subjects covered by or having the right to social security.

Exclusion Criteria:

• Subjects with known hypersensitivity to cysteamine and penicillamine.

• Females who are nursing, planning a pregnancy, known or suspected to be pregnant, or with a positive urinary pregnancy test.

• Subjects who, in the opinion of the Investigator, are not able or willing to comply with the protocol.

• Contra-indication to MRI assessment

CONTROLS FOR METABONOMIC ASSESSMENTS

Inclusion Criteria:

• Age and sex matched to study population: Age range: patients aged 4 to 5 years, 6 to 11 years, patients aged 12 to 17 years, adult patients: 18 or above.

Sex: male or female

• Subjects or their parent or legal guardian must provide written informed consent prior to participation in the study.

• Subjects covered by or having the right to social security.

Exclusion Criteria:

• Any uropathology or nephropathology.

CONTROLS FOR NMRS ASSESSMENTS

Inclusion Criteria:

• Age and sex matched to study population: Age range: patients aged 4 to 5 years, 6 to 11 years, patients aged 12 to 17 years, adult patients: 18 or above.

Sex: male or female

• Subjects or their parent or legal guardian must provide written informed consent prior to participation in the study.

• Subjects covered by or having the right to social security.

Exclusion Criteria:

• Any uropathology or nephropathology.

• Any neurological and/or psychiatric disorder

• Contra-indication to MRI assessment.

Related Conditions & MeSH terms

• Cystinosis

Intervention

Other:
• Cysteamine bitartrate
No intervention

Locations

Country	Name	City	State
France	Hospices Civils de Lyon	Lyon

Sponsors (1)

Lead Sponsor	Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	WBC cystine levels	PD measurements will be performed at D1, M1, M3, M6, M9, M12, M15, M18, M21 and M24.; Compliance under cysteamine will be measured from D1 to M24 using electronic devices (date and time of bottle opening are recorded), accountability of study treatment and information of patients' diary. Compliance measurement between two consecutive study visits will be expressed as the proportion of the observed number of opening compared to the expected number and the cumulated dose taken compared to the expected dose.Compliance will be first considered as a dichotomous variable, the compliance being described as satisfactory if greater than 95% during a specific period.Compliance will then be considered as a quantitative variable	Day1and every three months : Month1, Month3, Month6, Month9, Month12, Month15, Month18, Month21 and Month24.
Secondary	Presence or absence and accountability of cystine crystals.	Eye examination	Every 6 month : Month1, Month6, Month12, Month18, Month24
Secondary	Memory and visuoperceptual tests repeated during the study		at Day 1 and two years
Secondary	presence or absence of cystine accumulation, determination of the sites of cystine accumulation in the CNS and relationship with the compliance to cysteamine treatment, relationship with neuropsychological status.	NMRS assessments	at Month 1 and two years
Secondary	Concentration of cysteamine in the CSF, associated to a measurement of the CSF pressure		at any visit
Secondary	concentration of cysteamine in blood (measured by toxicological HPLC analysis with fluorescence detection)		at Day1 and every 3 months : month1, month3, month6, month9, month12, month15, month18, month21, month24
Secondary	discrimination of urine and blood samples,from metabolic spectroscopic data obtained by nuclear magnetic resonance.	Perturbed metabolic network resulting from the intake of cysteamine in comparison to controls,using urine and blood samples available for patients with cystinosis and their controls	Every 3 months during 6 months and every 6 months to month 6 until two years
Secondary	Concentration effect, dose effect model.	pharmacokinetic profile and 2 timepoints pharmacodynamics.	at month 6