Long-Term Study of Nitisinone to Treat Alkaptonuria

• Sponsor: National Human Genome Research Institute (NHGRI) (NIH)
• Overall Status: Completed
• CT.gov ID: NCT00107783
• Collaborator: (none)
• Enrollment: 40
• Location: 1
• Arms: 2
• Duration (Months): 51
• Patients Per Site Per Month: 0.8

Study Details

Study Description

Brief Summary

This 3-year study will examine the safety and effectiveness of long-term use of nitisinone (Orfadin) for treating joint problems in patients with alkaptonuria, an inherited disease in which a compound called homogentisic acid accumulates. The excess homogentisic acid causes arthritis and limited joint movement. It can also cause heart valve damage and kidney stones.

Patients between 30 and 80 years of age with alkaptonuria may be eligible for this study. Patients must have hip involvement, but at least one remaining hip joint. Candidates are recruited from among patients enrolled in protocol 00-HG-0141, "Clinical, Biochemical, and Molecular Investigations into Alkaptonuria." Participants may enter both protocols simultaneously.

Participants are randomly assigned to one of two treatment groups: one group takes their regular medicines plus a 2-mg nitisinone capsule daily; the other group takes only their regular medicines. Patients taking nitisinone have blood tests to measure liver function 2 weeks and 6 weeks after starting treatment. Before starting therapy, all patients are admitted to the NIH Clinical Center for 4-5 days to undergo the following procedures:

• Medical history and physical examination

• 24-hour urine collection to test for sugar, protein, and other molecules

• Blood tests for liver and thyroid function, blood counts, and blood chemistries

• Blood and urine tests to measure tyrosine and other amino acids and homogentisic acid

• Bone x-rays

• Spiral CT (computed tomography) of the abdomen to detect kidney stones

• Eye examination and evaluations by specialists in rehabilitation medicine and pain, plus other consults in skin, brain, lung, heart, and kidney, as needed

All patients, whether or not they receive nitisinone, return to the Clinical Center for a 2-3 day follow-up admission every 4 months for a history and physical examination, blood tests, and two 24-hour urine collections. Every 12 months (12, 24 and 36 months after starting the study), patients also have repeat bone x-rays, spiral CT, kidney ultrasound, echocardiogram, and electrocardiogram. An Magnetic Resonance Imaging (MRI) of the brain is done at the end of the study.

Sixteen months after the end of the study enrollment period, the treated and non-treated groups are evaluated. If nitisinone has delayed the progression of joint disease in the treated group, the study continues and all patients receive the drug for the remainder of the study. If not, the study continues for another 20 months, at which time the study ends and the evaluation process is repeated.

Patients who develop symptoms such as corneal crystals, pain, or severe liver or nervous system toxicity may be taken off the study.

Condition or Disease	Intervention/Treatment	Phase
Alkaptonuria	Drug: Nitisinone (NTBC)	Phase 2

Detailed Description

Alkaptonuria is a rare metabolic disease in which homogentisic acid (HGA), an intermediary metabolite in tyrosine catabolism, accumulates due to deficiency of the enzyme homogentisic acid oxidase. Patients with alkaptonuria exhibit homogentisic aciduria and ochronosis, or dark pigmentation of various tissues due to binding of HGA and its oxidized metabolites. The ochronosis results in debilitating destruction of cartilage, arthritis, lumbosacral ankylosis, limitation of motion, and bone deterioration in later life. No effective therapy exists for alkaptonuria. However, a compound named 2-(2-nitro-4-trifluoromethylbenzoyl) - 1, 3-cyclohexanedione (nitisinone, NTBC, Orfadin) inhibits 4-hydroxyphenylpyruvate dioxygenase, the enzyme that produces HGA. Nitisinone, at doses of approximately 1 mg/kg/day, has proven safe and effective in tyrosinemia type I, which causes fatal liver disease in infants and children. Under protocol 97-HG-0201, we treated 9 alkaptonuria patients with nitisinone; for the 7 who received 1.05 mg twice daily, the HA fell from 4.0 plus or minus 1.8 g/24h to 0.2 plus or minus 0.2 g/24h (normal 0.028 plus or minus 0.015 g/24h, n=10). Plasma tyrosine levels rose from 67 plus or minus 18 micro M to 760 plus or minus 181 micro M. The current protocol (05-HG-0076) is a randomized, controlled clinical trial to determine if nitisinone (2 mg daily) is beneficial for the joint symptoms of alkaptonuira. Patients are examined at the NIH Clinical Research Center every 4 months for 3 years. Hip joint range of motion (ROM) serves as the primary outcome parameter, and nitisinone (Orfadin) is provided by Swedish Orphan International through an Investigational New Drug Application (IND), obtained by William A. Gahl. Forty patients (20 with nitisinone treatment and 20 untreated) have been enrolled for at least 16 months, and an interim analysis shows promising results. Serious adverse events in patients on nitisinone have included a death from myocardial infarction, keratopathy, and elevated liver function tests related to gallstones.

Study Design

• Study Type: Interventional
• Actual Enrollment: 40 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: Long-Term Clinical Trial of Nitisinone in Alkaptonuria
• Study Start Date: Jan 1, 2005
• Actual Primary Completion Date: Apr 1, 2009
• Actual Study Completion Date: Apr 1, 2009

Arms and Interventions

Arm	Intervention/Treatment
No Intervention: Control No treatment
Experimental: Nitisinone-treated Subjects received nitisinone 2 mg orally, once daily.	Drug: Nitisinone (NTBC); Treatment; Other Names: Orfadin

Outcome Measures

Primary Outcome Measures

1. Change in Total ROM Worse Hip [Measured at baseline and at 36 months]

   Change from baseline in the total (external + internal) hip range of motion (ROM) in the worse hip at 36 months. The patient lies on exam table in the supine position. The patient flexes his/her hip and knee to 90 degrees. The examiner measures the patient's hip external rotation and hip internal rotation range of motion with a goniometer.

Secondary Outcome Measures

1. Change in Schober's Test [Measured at baseline and at 36 months]

   Change from baseline of Schober's test at 36 months. Schober's test measures a patient's ability to flex his/her lower back. The examiner makes a mark at L5 (fifth lumbar vertebra) and places one finger 5 cm below and another finger 10 cm above this mark. The patient is asked to touch his/her toes. The examiner measures the increase in distance between the two fingers.

2. Change in Functional Reach Assessment [Measured at baseline and at 36 months]

   Change from baseline of functional reach assessment at 36 months. Functional reach assessment measures the difference between the length of a person's outstretched arm and their maximal reach forward, while maintaining balance.

3. Change in Timed Get up and go [Measured at baseline and at 36 months]

   Change from baseline of timed get up and go at 36 months. In timed get up and go, the patient is asked to stand up from a standard chair and walk a distance of 3 meters, turn around and walk back to the chair and sit down. The examiner measures the time it takes for the patient to perform this series of tasks.

4. Change in 6 Minute Walk Test (6MWT) [Measured at baseline and at 36 months]

   Change from baseline of the 6MWT at 36 months. The 6MWT measures the distance that a patient can quickly walk on a flat hard surface in a period of six minutes.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 30 Years to 80 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

• INCLUSION CRITERIA:

• Age 30-80 years, either gender

• Diagnosis of alkaptonuria based upon urinary HGA excretion greater than 0.4 g/24h

• At least one hip joint remaining

• Some evidence of hip involvement, e.g., pain or decreased range of motion

• Ability to travel to the NIH Clinical Research Center for admissions

• Ability to consent

• Availability of local medical follow-up

EXCLUSION CRITERIA:

• Age less than 30 or greater than 80

• Non-alkaptonuria causes of ochronosis

• Bilateral hip joint replacement

• Keratopathy

• Contact lenses

• Uncontrolled glaucoma

• History of myocardial infarction

• History of emphysema or pulmonary insufficiency (Forced vital capacity less than 70%)

• Psychiatric illness or neurological disease that interferes with compliance or communication with health care personnel

• Current malignancy

• Open skin lesions

• Dietary habits or use of homeopathic therapies that interfere with tyrosine catabolism. The diet must be reasonably balanced, as determined by a dietician.

• Uncontrolled hypertension (blood pressure greater than 180 systolic or greater than 95 diastolic)

• History of extreme alcohol abuse or sever liver disease

• Liver greater than 3 cm below the right costal margin

• Electrocardiogram changes indicative of myocardial infarction, arrhythmia, tachycardia, bradycardia, left bundle branch block

• Chest radiographic abnormalities, including an infiltrate, mass, congestive heart failure, embolism, atelectasis

• Serum postassium less than 3. 0 mEq/L

• Serum creatinine greater than 2.0 mg/dL

• Serum glutamic-pyruvic transaminase (SGPT) greater than 41 U/L or Serum glutamic-oxaloacetic transaminase (SGOT) greater than 34 U/L

• Creatine kinase (CK) greater than 500 U/L

• Hemoglobin less than 10.0 g/dL

• Platelets less than 100 k/mm(3)

• White blood cells (WBCs) less than 3.0 k/microL

• Free thyroxine (T4) greater than 15 microg/dL

• T4 less than 4 microg/dL

• Erythrocyte sedimentation rate (ESR) greater than 100 mm/h

• Plasma tyrosine greater than 150 microM

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	National Institutes of Health Clinical Center, 9000 Rockville Pike	Bethesda	Maryland	United States	20892

Sponsors and Collaborators

• National Human Genome Research Institute (NHGRI)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• NIH Clinical Center Detailed Web Page

Publications

• Introne WJ, Phornphutkul C, Bernardini I, McLaughlin K, Fitzpatrick D, Gahl WA. Exacerbation of the ochronosis of alkaptonuria due to renal insufficiency and improvement after renal transplantation. Mol Genet Metab. 2002 Sep-Oct;77(1-2):136-42.
• Janocha S, Wolz W, Srsen S, Srsnova K, Montagutelli X, Guénet JL, Grimm T, Kress W, Müller CR. The human gene for alkaptonuria (AKU) maps to chromosome 3q. Genomics. 1994 Jan 1;19(1):5-8.
• Phornphutkul C, Introne WJ, Perry MB, Bernardini I, Murphey MD, Fitzpatrick DL, Anderson PD, Huizing M, Anikster Y, Gerber LH, Gahl WA. Natural history of alkaptonuria. N Engl J Med. 2002 Dec 26;347(26):2111-21.

• ClinicalTrials.gov Identifier: NCT00107783
• Other Study ID Numbers: 050076; 05-HG-0076
• First Posted: Apr 8, 2005
• Last Update Posted: Aug 26, 2021
• Last Verified: Dec 1, 2010

• Keywords provided by , ,: Arthritis; Homogentisic Acid; Corneal Damage; Tyrosine; Alkaptonuria; Photophobia; Nitisinone
• Additional relevant MeSH terms: Alkaptonuria; Ochronosis; Nitisinone

Study Results

Participant Flow

Recruitment Details	Patients were enrolled at the NIH Clinical Center between April 2005 and March 2006.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Period Title: Overall Study
STARTED	20	20
COMPLETED	17	16
NOT COMPLETED	3	4

Baseline Characteristics

Arm/Group Title	Control	Nitisinone-treated	Total
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.	Total of all reporting groups
Overall Participants	20	20	40
Age (Count of Participants)
<=18 years	0 0%	0 0%	0 0%
Between 18 and 65 years	20 100%	19 95%	39 97.5%
>=65 years	0 0%	1 5%	1 2.5%
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]	51.3 (6.5)	52.2 (7.9)	51.7 (7.1)
Sex: Female, Male (Count of Participants)
Female	5 25%	8 40%	13 32.5%
Male	15 75%	12 60%	27 67.5%
Region of Enrollment (participants) [Number]
United States	20 100%	20 100%	40 100%
Total Range of Motion (ROM) Worse Hip (degrees) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [degrees]	46.4 (16.1)	39.0 (12.7)	42.7 (14.8)
Schober's test (cm) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [cm]	11.42 (1.04)	10.86 (0.73)	11.14 (0.93)
Functional Reach Assessment (cm) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [cm]	10.22 (2.92)	8.98 (3.10)	9.60 (3.04)
Timed get up and go (seconds) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [seconds]	7.56 (1.40)	9.70 (4.10)	8.63 (3.21)
6 minute walk test (ft) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [ft]	1578 (205)	1336 (369)	1457 (319)

Outcome Measures

1. Primary Outcome

Title	Change in Total ROM Worse Hip
Description	Change from baseline in the total (external + internal) hip range of motion (ROM) in the worse hip at 36 months. The patient lies on exam table in the supine position. The patient flexes his/her hip and knee to 90 degrees. The examiner measures the patient's hip external rotation and hip internal rotation range of motion with a goniometer.
Time Frame	Measured at baseline and at 36 months

Outcome Measure Data

Analysis Population Description

Intention to treat.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Measure Participants	20	20
Mean (Standard Deviation) [degrees]	-9.1 (24.7)	1.6 (21.8)

2. Secondary Outcome

Title	Change in Schober's Test
Description	Change from baseline of Schober's test at 36 months. Schober's test measures a patient's ability to flex his/her lower back. The examiner makes a mark at L5 (fifth lumbar vertebra) and places one finger 5 cm below and another finger 10 cm above this mark. The patient is asked to touch his/her toes. The examiner measures the increase in distance between the two fingers.
Time Frame	Measured at baseline and at 36 months

Outcome Measure Data

Analysis Population Description

In the control group, two patients who dropped out for personal reasons were not included in this analysis, and in the treated group one patient who died was not included in this analysis.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Measure Participants	18	19
Mean (Standard Deviation) [cm]	-0.06 (1.33)	0.12 (1.05)

3. Secondary Outcome

Title	Change in Functional Reach Assessment
Description	Change from baseline of functional reach assessment at 36 months. Functional reach assessment measures the difference between the length of a person's outstretched arm and their maximal reach forward, while maintaining balance.
Time Frame	Measured at baseline and at 36 months

Outcome Measure Data

Analysis Population Description

In the control group, two patients who dropped out for personal reasons were not included in this analysis, and in the treated group one patient who died was not included in this analysis.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Measure Participants	18	19
Mean (Standard Deviation) [cm]	-1.21 (3.81)	-1.86 (3.59)

4. Secondary Outcome

Title	Change in Timed Get up and go
Description	Change from baseline of timed get up and go at 36 months. In timed get up and go, the patient is asked to stand up from a standard chair and walk a distance of 3 meters, turn around and walk back to the chair and sit down. The examiner measures the time it takes for the patient to perform this series of tasks.
Time Frame	Measured at baseline and at 36 months

Outcome Measure Data

Analysis Population Description

In the control group, two patients who dropped out for personal reasons were not included in this analysis, and in the treated group one patient who died was not included in this analysis.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Measure Participants	18	19
Mean (Standard Deviation) [seconds]	-0.54 (1.84)	-1.33 (5.04)

5. Secondary Outcome

Title	Change in 6 Minute Walk Test (6MWT)
Description	Change from baseline of the 6MWT at 36 months. The 6MWT measures the distance that a patient can quickly walk on a flat hard surface in a period of six minutes.
Time Frame	Measured at baseline and at 36 months

Outcome Measure Data

Analysis Population Description

In the control group, two patients who dropped out for personal reasons were not included in this analysis, and in the treated group one patient who died was not included in this analysis.

Arm/Group Title	Control	Nitisinone-treated
Arm/Group Description	No treatment	Subjects received nitisinone 2 mg orally, once daily.
Measure Participants	18	19
Mean (Standard Deviation) [ft]	22 (356)	169 (591)

Adverse Events

Time Frame	36 months
Arm/Group Title	Control		Nitisinone-treated
Arm/Group Description	No treatment		Subjects received nitisinone 2 mg orally, once daily.
All Cause Mortality
	Control		Nitisinone-treated
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	/ (NaN)		/ (NaN)
Serious Adverse Events
	Control		Nitisinone-treated
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	0/20 (0%)		6/20 (30%)
Blood and lymphatic system disorders
anemia	0/20 (0%)	0	1/20 (5%)	1
Cardiac disorders
atrial fibrillation	0/20 (0%)	0	1/20 (5%)	1
Eye disorders
keratitis	0/20 (0%)	0	1/20 (5%)	3
Hepatobiliary disorders
bile duct stone	0/20 (0%)	0	1/20 (5%)	1
liver enzyme elevation	0/20 (0%)	0	1/20 (5%)	1
Immune system disorders
sarcoidosis	0/20 (0%)	0	1/20 (5%)	1
Injury, poisoning and procedural complications
accidental overdose	0/20 (0%)	0	1/20 (5%)	1
muscle injury	0/20 (0%)	0	1/20 (5%)	1
Other (Not Including Serious) Adverse Events
	Control		Nitisinone-treated
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	10/20 (50%)		10/20 (50%)
Ear and labyrinth disorders
sensorineural hearing loss	0/0 (NaN)	0	3/20 (15%)	3
Hepatobiliary disorders
elevated liver enzymes	6/20 (30%)	8	6/20 (30%)	8
Infections and infestations
upper respiratory infection	5/20 (25%)	6	2/20 (10%)	2
Psychiatric disorders
depression	2/20 (10%)	2	0/20 (0%)	0
Skin and subcutaneous tissue disorders
skin rash	3/20 (15%)	3	0/20 (0%)	0

Limitations/Caveats

Small number of patients involved in study and several patients dropped out; primary outcome parameter selection possibly inappropriate because hip joint damage that is already present may be irreversible.

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.