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Tyrosinemias clinical trials

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NCT ID: NCT05062226 Completed - PKU Clinical Trials

GMP Case Studies of Tolerance, Safety and Acceptability in PKU and TYR

Start date: September 16, 2020
Phase: N/A
Study type: Interventional

Three new protein substitutes have been developed to help with compliance in PKU and TYR patients, which are powdered protein substitutes, low in Phe and, low in Phe and Tyr respectively, with a mixed balance of glycomacropeptide (GMP), essential and non-essential amino acids, carbohydrates, fats and micronutrients for the dietary management of PKU and TYR. This series of case-studies will evaluate the acceptability, compliance, gastrointestinal tolerance and safety of the three GMP-based products for PKU and TYR in 45 patients with PKU and TYR, in both adults and children over 3 years (15 patients per product). The case study will last 29 days in total, including a 1-day baseline period followed by a 28-day intervention period. The case studies will be conducted across multiple specialist metabolic centres in the UK, to meet the UK ACBS and GMS requirements for acceptability studies. A series of case studies is undertaken due to the rarity of these conditions and the difficulty in recruiting these patients to trials.

NCT ID: NCT04196959 Completed - Alkaptonuria Clinical Trials

Evaluation of TYR Sphere

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

For 28 days, 20 patients with tyrosinaemia will take TYR sphere as part of the usual dietary management of their condition. Patients will record their adherence to recommended intakes each day, gastrointestinal symptoms (if any) experienced each day of weeks one and four, and the palatability of the product at the end of the trial. Metabolic control will be evaluated by dried blood spots collected during the Baseline and End of Study visits, and weekly during the 28 days of the study itself. Trial data will be used in an application to make TYR sphere available via the NHS.

NCT ID: NCT02750709 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Bioequivalence Study of Two Nitisinone Formulations Compared to Orfadin

Start date: October 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Nitisinone 10 mg Tablets (Test Product 1) and Nitisinone 10 mg Tablets High Compritol (Test Product 2) are bioequivalent to the reference product Orfadin 10 mg capsules.

NCT ID: NCT02750345 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Bioequivalence Study of Two Oral Nitisinone Formulations to Treat Hereditary Tyrosinemia (HT-1)

Start date: March 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Nitisinone 10 mg Tablets (Test Product 1) and Nitisinone 10 mg Tablets 'Baked' for 6 months @ 40°C/75% RH (Test Product 2) are bioequivalent to the reference product Orfadin 10 mg hard capsules.

NCT ID: NCT02750332 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia (HT-1)

Start date: November 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare the bioavailability of the Test Product, Nitisinone 10 mg Tablet, under fasting and fed conditions (food-effect).

NCT ID: NCT02323529 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Efficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Nitisinone in HT-1

HT-1
Start date: December 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to look at the steady-state serum concentrations of nitisinone when switching from twice daily and once daily dosing.

NCT ID: NCT02320084 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Long Term Safety Study of Orfadin Treatment in HT-1 Patients in Standard Clinical Care

OPAL
Start date: September 2013
Phase:
Study type: Observational

The purpose of this study is to look at the long term safety profile of Orfadin treatment in patients suffering from hereditary tyrosinemia type 1 (HT-1). Patients included in the study will use Orfadin according to normal clinical practice.

NCT ID: NCT01734889 Completed - Clinical trials for Hereditary Tyrosinemia, Type I

Taste and Palatability of Orfadin Suspension

Start date: October 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to verify that pediatric patients, especially those who are not old enough to swallow capsules, accept the taste and palatability of a new suspension.

NCT ID: NCT00004443 Completed - Tyrosinemia I Clinical Trials

Study of NTBC for Tyrosinemia I

Start date: October 1998
Phase: N/A
Study type: Interventional

OBJECTIVES: I. Assess the safety and efficacy of NTBC in children with tyrosinemia I. II. Evaluate the effects of NTBC on survival, rate of neurologic crises, improvement in renal tubular damage, reduction in the need for liver transplantation, and reduction in the development of hepatocarcinoma in these patients.

NCT ID: NCT00004333 Completed - Tyrosinemia, Type I Clinical Trials

Phase II Study of the Enzyme Inhibitor NTBC for Tyrosinemia Type I

Start date: November 1994
Phase: Phase 2
Study type: Interventional

OBJECTIVES: Assess whether 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC) at 0.6 mg/kg per day prevents liver failure in at least 1 patient with tyrosinemia type I.