Nitisinone for Type 1B Oculocutaneous Albinism

• Status: Completed
• Trial end date: 2017-02-07
• Target enrollment: 0
• Participant gender: All

Summary

Background:

• Oculocutaneous albinism, type 1B (OCA1B) is a genetic disease caused by problems in the gene that makes tyrosine. Tyrosine is an amino acid needed to produce pigment in the skin, hair, and eyes. People with OCA1B have pale skin, white hair, and light-colored eyes. Pigment in the back of the eye helps vision, so people with OCA-1B often have visual problems. Researchers want to see if a drug called nitisinone can help improve eye pigmentation and vision in people with OCA1B. Nitisinone is approved for treating a related genetic disease that causes problems with tyrosine, so it may help people with OCA1B.

Objectives:

• To see if nitisinone can help improve eye pigmentation and vision in people with OCA1B.

Eligibility:

• Individuals at least 18 years of age who have OCA1B.

Design:

• This study will last about 18 months. It requires eight outpatient visits, each about 3 months apart. Each visit will require 1 to 2 days of testing.

• Participants will be screened with a physical exam, eye exam, and medical history. They will have additional vision and neurological tests. They will be tested to see how their brain and retinas respond to light. They will also take hair and blood samples, and answer questions about diet.

• Participants will receive the study drug. They will take one pill a day for 1 year. They will keep track of the dose in a study diary.

• At the outpatient visits, participants will have the following tests:

• Medical history and physical exam

• Neurological and eye exams

• Retina function tests

• Tests of the skin and brain's response to light

• Blood and urine tests

• Dietary consultation

• Visual function questionnaire.

• After the end of the study, participants will return to the care of their regular eye doctor.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Eye Institute (NEI)
• Collaborator: National Human Genome Research Institute (NHGRI)
• Treatments: Nitisinone

Criteria

• INCLUSION CRITERIA:

To be eligible, the following inclusion criteria must be met, when applicable.

1. Participant must be 18 years of age or older.

2. Participant must understand and sign the protocol s informed consent document.

3. 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).

4. 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.

5. 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).

6. Participant must have OCA1B, as defined by ALL (a-d) of the following criteria:

1. 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.

2. Predominant contralateral decussation of ganglion cell axons, as determined by pattern visual evoked potential (VEP).

3. Participant has at least one definitive mutation in the OCA1 gene (tyrosinase).

4. 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:

1. Serum potassium < 3.0 mEq/L,

2. Serum CK > 500 U/L,

3. Hemoglobin < 10.0 g/dL,

4. White blood cell (WBC) count < 3.0 k/microL,

5. Plasma tyrosine > 150 microM,

6. ESR > 100 mm/h, and/or

7. 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.