241. 高チロシン血症1型 Hypertyrosinemia type I Clinical trials / Disease details
臨床試験数 : 14 / 薬物数 : 7 - (DrugBank : 1) / 標的遺伝子数 : 1 - 標的パスウェイ数 : 5
Showing 1 to 10 of 14 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT04113772 (ClinicalTrials.gov) | November 1, 2019 | 1/10/2019 | Bio Equivalency 20 Mgm Orfadin and 20 Mgm of Nitisonine | Orfadin and Nitinosine Study | Hereditary Tyrosinemia, Type I | Drug: Nitisinone;Drug: Orfadin | Sutphin Drugs | NULL | Not yet recruiting | 18 Years | 50 Years | All | 4 | N/A | India |
2 | NCT02750345 (ClinicalTrials.gov) | March 2016 | 21/4/2016 | Bioequivalence Study of Two Oral Nitisinone Formulations to Treat Hereditary Tyrosinemia (HT-1) | A Three-Period Crossover Study to Determine the Bioequivalence of Two Oral Formulations Containing Nitisinone 10 mg Compared to Reference Formulation Orfadin In Healthy Subjects Under Fasting Conditions A Three-Period Crossover Study to Determine the Bioequivalence of Two Oral Formulations Containing N ... | Hereditary Tyrosinemia, Type I | Drug: Nitisinone;Drug: Nitisinone Baked Tablet;Drug: Orfadin | Cycle Pharmaceuticals Ltd. | Parexel | Completed | 18 Years | 55 Years | All | 24 | Phase 1 | South Africa |
3 | NCT02750332 (ClinicalTrials.gov) | November 2015 | 21/4/2016 | Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia (HT-1) Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia ... | A Single Center, Single-Dose, Open-Label, Randomized Study to Compare the Bioavailability of an Oral Test Formulation Containing Nitisinone 10 mg in at Least 16 Healthy Male and Female Subjects Under Fasting and Fed Conditions A Single Center, Single-Dose, Open-Label, Randomized Study to Compare the Bioavailability of an Oral ... | Hereditary Tyrosinemia, Type I | Drug: Nitisinone | Cycle Pharmaceuticals Ltd. | Parexel | Completed | 18 Years | 55 Years | All | 20 | Phase 1 | South Africa |
4 | NCT02750709 (ClinicalTrials.gov) | October 2015 | 20/4/2016 | Bioequivalence Study of Two Nitisinone Formulations Compared to Orfadin | A Single Center, Single-Dose, Open-Label, Laboratory-Blind, Randomized, Three-Period Crossover Study to Determine the Bioequivalence of Two Oral Formulations Containing of Nitisinone 10 mg Compared to the Reference Formulation Orfadin 10 mg in at Least 18 Healthy Male and Female Subjects Under Fasting Conditions A Single Center, Single-Dose, Open-Label, Laboratory-Blind, Randomized, Three-Period Crossover Study ... | Hereditary Tyrosinemia, Type I | Drug: Nitisinone;Drug: Nitisinone 10 mg Tablet High Compritol;Drug: Orfadin | Cycle Pharmaceuticals Ltd. | Parexel | Completed | 18 Years | 55 Years | All | 24 | Phase 1 | South Africa |
5 | EUCTR2013-004132-29-DK (EUCTR) | 16/12/2014 | 25/08/2014 | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | hereditary tyrosinemia type 1 MedDRA version: 17.1;Level: LLT;Classification code 10069462;Term: Tyrosinemia type I;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Metabolic Phenomena [G03] hereditary tyrosinemia type 1 MedDRA version: 17.1;Level: LLT;Classification code 10069462;Term: Tyr ... | Trade Name: Orfadin INN or Proposed INN: NITISINONE | Swedish Orphan Biovitrum AB (Publ) | NULL | Not Recruiting | Female: yes Male: yes | 20 | Belgium;Denmark;Sweden | |||
6 | NCT02323529 (ClinicalTrials.gov) | December 2014 | 18/12/2014 | Efficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Nitisinone in HT-1 | Open-label, Multicentre, Multiple-dose Trial to Evaluate Pharmacokinetics, Efficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Orfadin in Patients Diagnosed With Hereditary Tyrosinemia Type 1 Open-label, Multicentre, Multiple-dose Trial to Evaluate Pharmacokinetics, Efficacy and Safety of On ... | Hereditary Tyrosinemia, Type I | Drug: Nitisinone | Swedish Orphan Biovitrum | NULL | Completed | N/A | N/A | Both | 18 | Phase 3 | Belgium;Denmark;France;Germany;Sweden |
7 | EUCTR2013-004132-29-BE (EUCTR) | 06/11/2014 | 15/10/2014 | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | hereditary tyrosinemia type 1 MedDRA version: 17.0;Level: LLT;Classification code 10069462;Term: Tyrosinemia type I;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Metabolic Phenomena [G03] hereditary tyrosinemia type 1 MedDRA version: 17.0;Level: LLT;Classification code 10069462;Term: Tyr ... | Trade Name: Orfadin INN or Proposed INN: NITISINONE Trade Name: Orfadin INN or Proposed INN: NITISINONE Trade Name: Orfadin INN or Proposed INN: NITISINONE Trade Name: Orfadin INN or Proposed INN: NITISINONE Trade Name: Orfadin INN or Proposed INN: NITISINONE ... | Swedish Orphan Biovitrum AB (Publ) | NULL | Not Recruiting | Female: yes Male: yes | 20 | Phase 4 | Belgium;Denmark;Sweden | ||
8 | EUCTR2013-004132-29-SE (EUCTR) | 15/10/2014 | 18/08/2014 | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, efficacy and safety of once daily dosing compared to twice daily dosing of Orfadin in patients diagnosed with hereditary tyrosinemia type 1 An open-label, non-randomized, sequential, multicenter study to evaluate the pharmacokinetics, effic ... | hereditary tyrosinemia type 1 MedDRA version: 17.1;Level: LLT;Classification code 10069462;Term: Tyrosinemia type I;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Metabolic Phenomena [G03] hereditary tyrosinemia type 1 MedDRA version: 17.1;Level: LLT;Classification code 10069462;Term: Tyr ... | Trade Name: Orfadin INN or Proposed INN: NITISINONE | Swedish Orphan Biovitrum AB (Publ) | NULL | Not Recruiting | Female: yes Male: yes | 20 | Belgium;Denmark;Sweden | |||
9 | NCT02320084 (ClinicalTrials.gov) | September 2013 | 23/10/2014 | Long Term Safety Study of Orfadin Treatment in HT-1 Patients in Standard Clinical Care | A Non-interventional Post Authorization Study (PASS) to Evaluate Long-term Safety of Orfadin Treatment in Hypertyrosinemia Type 1 (HT-1) Patients in Standard Care A Non-interventional Post Authorization Study (PASS) to Evaluate Long-term Safety of Orfadin Treatme ... | Hereditary Tyrosinemia, Type I | Drug: Nitisinone | Swedish Orphan Biovitrum | NULL | Completed | N/A | N/A | All | 315 | Austria;Belgium;Czechia;Denmark;Finland;France;Germany;Hungary;Ireland;Italy;Netherlands;Norway;Poland;Portugal;Spain;Sweden;United Kingdom;Croatia;Czech Republic;Greece;Kosovo;Lithuania;Macedonia, The Former Yugoslav Republic of;Romania;Slovakia;Switzerland Austria;Belgium;Czechia;Denmark;Finland;France;Germany;Hungary;Ireland;Italy;Netherlands;Norway;Pola ... | |
10 | EUCTR2012-002286-36-DE (EUCTR) | 19/11/2012 | 03/08/2012 | Taste and palatability of Orfadin suspension. | Taste and palatability of Orfadin suspension. An open, non-controlled 3-day study in pediatric patients with hereditary tyrosinemia type 1 treated with Orfadin. Taste and palatability of Orfadin suspension. An open, non-controlled 3-day study in pediatric patie ... | Hereditary tyrosinemia type 1 (HT-1) MedDRA version: 14.1;Level: LLT;Classification code 10069459;Term: Tyrosinaemia type I;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Metabolic Phenomena [G03] Hereditary tyrosinemia type 1 (HT-1) MedDRA version: 14.1;Level: LLT;Classification code 10069459;Te ... | Product Name: Orfadin oral suspension 4mg/ml INN or Proposed INN: Nitisinone | Swedish Orphan Biovitrum AB | NULL | Not Recruiting | Female: yes Male: yes | 18 | Germany;United Kingdom |