- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Stargardt disease.
Displaying page 1 of 1.
| EudraCT Number: 2012-001990-95 | Sponsor Protocol Number: LTS13588-(SG1/002/11) | Start Date*: 2012-11-09 | |||||||||||
| Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
| Full Title: An Open Label Study to Determine the Long Term Safety, Tolerability and Biological Activity of SAR422459 in Patients with Stargardt’s Macular Degeneration | |||||||||||||
| Medical condition: Stargardt Macular Dystrophy, also known as fundus flavimaculatus or Stargardt disease. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004783-35 | Sponsor Protocol Number: OPH2005 | Start Date*: 2018-07-10 | |||||||||||
| Sponsor Name:IVERIC bio | |||||||||||||
| Full Title: A Phase 2b Randomized, Double-masked, Controlled Trial to Establish the Safety and Efficacy of Zimura™ (Complement C5 Inhibitor) Compared to Sham in Subjects with Autosomal Recessive Stargardt Disease | |||||||||||||
| Medical condition: Autosomal Recessive Stargardt Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) GB (GB - no longer in EU/EEA) HU (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001496-20 | Sponsor Protocol Number: SMR3438 | Start Date*: 2019-05-14 | |||||||||||
| Sponsor Name:Katairo GmbH | |||||||||||||
| Full Title: A multi-national, multi-centre, double-masked, placebo-controlled proof of concept trial to evaluate the safety and efficacy of oral soraprazan in Stargardt disease | |||||||||||||
| Medical condition: Stargardt Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023111-34 | Sponsor Protocol Number: SG1/001/10 | Start Date*: 2011-07-18 |
| Sponsor Name:Oxford BioMedica (UK) Ltd | ||
| Full Title: A Phase I/IIa Dose Escalation Safety Study of Subretinally Injected StarGen, Administered to Patients with Stargardt's Macular Degeneration. | ||
| Medical condition: Stargardt Macular Dystrophy, also known as fundus flavimaculatus or Stargardt disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) NL (Not Authorised) IT (Prematurely Ended) Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003498-82 | Sponsor Protocol Number: 4429-301 | Start Date*: 2019-03-18 | |||||||||||
| Sponsor Name:Acucela Inc. | |||||||||||||
| Full Title: A Phase 3 Multicenter, Randomized, Double-Masked Study Comparing the Efficacy and Safety of Emixustat Hydrochloride with Placebo for the Treatment of Macular Atrophy Secondary to Stargardt Disease | |||||||||||||
| Medical condition: Stargardt Disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DK (Completed) DE (Completed) ES (Ongoing) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003253-36 | Sponsor Protocol Number: LBS-008-CT03 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Belite Bio, Inc | ||
| Full Title: Phase 3, Multicenter, Randomized, Double-Masked, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Tinlarebant in the Treatment of Stargardt Disease in Adolescent Subjects | ||
| Medical condition: Stargardt Disease | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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