AAV5-HRKP.RPGR ( DrugBank: - )


1 disease
告示番号疾患名(ページ内リンク)臨床試験数
90網膜色素変性症13

90. 網膜色素変性症


臨床試験数 : 147 薬物数 : 176 - (DrugBank : 43) / 標的遺伝子数 : 49 - 標的パスウェイ数 : 110
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1EUCTR2020-002873-88-IE
(EUCTR)
19/07/202215/10/2021Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: Botaretigene Sparoparvovec
Product Code: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: Botaretigene Sparoparvovec
Product Code: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
96Phase 3United States;Spain;Ireland;Israel;Switzerland;Italy;United Kingdom;France;Canada;Belgium;Denmark;Netherlands;Germany
2EUCTR2020-002255-37-IE
(EUCTR)
26/05/202215/10/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
3EUCTR2020-002873-88-ES
(EUCTR)
28/03/202202/11/2021Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
4EUCTR2020-002255-37-ES
(EUCTR)
28/03/202202/11/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
5EUCTR2020-002255-37-NL
(EUCTR)
14/03/202222/10/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3Switzerland;United Kingdom;France;United States;Spain;Ireland;Israel;Italy;Canada;Belgium;Denmark;Netherlands;Germany
6EUCTR2020-002873-88-NL
(EUCTR)
14/03/202222/10/2021Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Netherlands;Germany
7EUCTR2020-002255-37-DK
(EUCTR)
01/03/202208/11/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
8EUCTR2020-002873-88-DK
(EUCTR)
01/03/202208/11/2021Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
9EUCTR2020-002873-88-Outside-EU/EEA
(EUCTR)
21/12/2022Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGRMeiraGTx UK II LimitedNULLNAFemale: yes
Male: yes
Phase 3Canada;Israel;United States;Switzerland;United Kingdom
10EUCTR2020-002255-37-BE
(EUCTR)
29/10/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLNAFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
11EUCTR2020-002873-88-BE
(EUCTR)
29/10/2021Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-HRKP.RPGR
MeiraGTx UK II LimitedNULLNAFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
12EUCTR2020-002255-37-FR
(EUCTR)
05/11/2021Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
Product Name: AAV5-hRKp.RPGR
INN or Proposed INN: botaretigene sparoparvovec
Other descriptive name: AAV5-hRKp.RPGR
MeiraGTx UK II LimitedNULLNAFemale: yes
Male: yes
66Phase 3United States;Spain;Ireland;Israel;Italy;Switzerland;United Kingdom;France;Canada;Belgium;Denmark;Germany;Netherlands
13EUCTR2020-002255-37-Outside-EU/EEA
(EUCTR)
21/12/2022Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa (progressive reduction in vision) due to a gene defect on Chromosome X.Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene - Long Term Follow-Up study of Gene Therapy Trial for Patients with Retinitis Pigmentosa: RPGR X-Linked Retinitis Pigmentosa caused by mutations in the RPGR gene
MedDRA version: 20.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11]
Product Name: AAV5-hRKp.RPGRMeiraGTx UK II LimitedNULLNAFemale: yes
Male: yes
Phase 3Canada;Israel;United States;Switzerland;United Kingdom