Terminé

A Pilot Study of Nitisinone in the Treatment of Oculocutaneous Albinism, Type 1B

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Ce qui est testé

Nitisinone

Médicament
Qui peut participer

Erreurs innées du métabolisme des acides aminés+17

+ Maladies oculaires

+ Maladies métaboliques

À partir de 18 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude thérapeutique

Phase 1 & 2
Interventionnel
Date de début : avril 2013
Voir le détail du protocole

Résumé

Sponsor principalNational Eye Institute (NEI)
Dernière mise à jour : 26 février 2019
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 16 avril 2013

Date à laquelle le premier participant a commencé l'étude.

Objective: The primary objective of this study is to evaluate oral nitisinone as a treatment that improves ocular pigmentation in adult participants with oculocutaneous albinism, type 1B (OCA1B). Secondary objectives of this study are to determine whether the selected outcome measures are robust enough to use in a larger trial and to assess whether oral nitisinone improves visual function, skin pigmentation, and hair pigmentation in participants with OCA1B. Study Population: Five participants with OCA1B will be enrolled initially. However, up to an additional three participants may be enrolled to account for participants who withdraw from the study for any reason before the Month 12 visit. Design: In this pilot, phase 1/2, single-site, prospective, open label trial, participants will receive 2 mg of oral nitisinone daily for at least one year, and they will be followed for at least 18 months. Ocular and non-ocular data will be collected at least every three months, with the first follow-up visit occurring three months after the final baseline visit. Participants will be required to have at least 8 outpatient visits at the NEI clinic over a period of 18 months. This study has a common termination date and therefore may continue for up to four years. Outcome Measures: The primary outcome for the study is the absolute mean change in iris pigmentation on an 8-point scale at 12 months as compared to baseline. Participants left and right eyes will be analyzed. The absolute mean change in iris pigmentation for each eye on an 8-point scale at 3, 6 and 9 months compared to baseline will be assessed as secondary outcomes. Other secondary outcomes include the absolute and percent change in semi-quantitative iris pigmentation on image analysis; the absolute change in electronic visual acuity (EVA) for each eye and binocular vision; the absolute change in contrast sensitivity without glare, with medium glare, and with high glare for binocular vision; the absolute change in full-field ERG measures for each eye; and the absolute and percent change in melanin content in skin using skin reflectometry at 3, 6, 9 and 12 months as compared to baseline; Qualitative changes in hair, skin, and fundus pigmentation at 3, 6, 9 and 12 months as compared to previous visit will be assessed. The absolute and percent change in hair melanin will also be assessed at 12 months as compared to baseline. The number and severity of adverse events and the number of withdrawals will be assessed as safety outcomes.

NCT01838655
Sponsor principalNational Eye Institute (NEI)
Dernière mise à jour : 26 février 2019
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

5 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Traitement

Cette étude teste un ou plusieurs traitements pour évaluer leur efficacité contre une maladie ou un problème de santé spécifique. L'objectif est de voir si un nouveau médicament ou une thérapie fonctionne mieux, ou provoque moins d'effets secondaires que les options existantes.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

À partir de 18 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Erreurs innées du métabolisme des acides aminésMaladies oculairesMaladies métaboliquesErreurs innées du métabolismeMaladies et anomalies congénitales, héréditaires et néonatalesMaladies du système nerveuxManifestations NeurologiquesMaladies nutritionnelles et métaboliquesTroubles de la pigmentationTroubles de la SensationSignes et symptômesMaladies de la peauMaladies génétiques de la peauConditions pathologiques, signes et symptômesMaladies oculaires héréditairesMaladies de la peau et des tissus conjonctifsHypopigmentationMaladies Génétiques CongénitalesAlbinismeTroubles de la vision

Critères

INCLUSION CRITERIA: To be eligible, the following inclusion criteria must be met, when applicable. Participant must be 18 years of age or older. Participant must understand and sign the protocol s informed consent document. Participant must have normal renal function, liver function, and platelet counts or have mild abnormalities no greater than grade 1 as defined by the Common Terminology Criteria for Adverse Events v4.0 (CTCAE). Any female participant of childbearing potential must have a negative pregnancy test at screening and must be willing to undergo pregnancy testing immediately prior to the start of the investigational product and while on the investigational product. Any female participant of childbearing potential and any male participant able to father children must have (or have a partner who has) had a hysterectomy or vasectomy, be completely abstinent from intercourse, or must agree to practice two effective methods of contraception while taking the investigational product and for at least two months following the last dose of investigational product. Acceptable methods of contraception include: Hormonal contraception (i.e., birth control pills, injected hormones, dermal patch, or vaginal ring), Intrauterine device, Barrier methods (diaphragm, condom) with spermicide, or Surgical sterilization (tubal ligation). Participant must have OCA1B, as defined by ALL (a-d) of the following criteria: Participant has ophthalmic signs or symptoms of albinism, including: Bilateral visual acuity E-ETDRS EVA letter score of less than or equal to 83 (i.e., Snellen equivalent of 20/25 or worse) that is not attributable to any other pathology. Bilateral iris transillumination that can be seen in clinical photographs. Predominant contralateral decussation of ganglion cell axons, as determined by pattern visual evoked potential (VEP). Participant has at least one definitive mutation in the OCA1 gene (tyrosinase). Participant has no definitive mutations in the OCA2 gene. EXCLUSION CRITERIA: Participant is pregnant or breast-feeding. Participant is a male AND has a definitive mutation in the OA1 gene. Participant has any of the following abnormal laboratory test results: Serum potassium < 3.0 mEq/L, Serum CK > 500 U/L, Hemoglobin < 10.0 g/dL, White blood cell (WBC) count < 3.0 k/microL, Plasma tyrosine > 150 microM, ESR > 100 mm/h, and/or Serum T4 > 15 microg/dL OR Serum T4 < 4 microg/dL. Participant has keratopathy. Participant has a current malignancy. Participant has open skin lesions. Participant is on a diet that deliberately increases protein intake to disproportionate levels (e.g., Atkins diet). The diet must be reasonably balanced, as determined by a dietician. Participant has uncontrolled hypertension, defined as systolic blood pressure above 180 mmHg or diastolic blood pressure above 95 mmHg. Participant has another chronic ocular disease that may confound the results of visual tests, such as age-related macular degeneration, cataract of possible visual significance, or uncontrolled glaucoma. Participant drinks more than the equivalent of two glasses of wine per day on average, has a history of alcohol abuse, or has a severe liver illness. Participant s liver is > 3 cm below the right costal margin. Participant has a muscle disease. Participant is currently taking a medication known to cause elevated liver function tests including statins/HMG-Co-A reductase inhibitors (e.g., lovastatin, simvastatin); anti-epileptic medications (e.g., carbamazepine, phenytoin, phenobarbital); tetracycline or its derivatives, if used chronically; acetaminophen, if used daily/chronically; amiodarone; and any other medications with known significant liver toxicity.

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

Un seul groupe d'intervention est désigné dans cette étude

Cette étude ne comporte pas de groupe placebo. 

Groupes de traitement

Groupe I

Expérimental
Oral administration of nitisinone

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 1 site

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesOuvrir National Institutes of Health Clinical Center, 9000 Rockville Pike dans Google Maps
Terminé1 Centres d'Étude