- ICH GCP
- US Clinical Trials Registry
- Researchers
- Canada
- Retinal Diseases
Medical specialists from Canada tagged as investigators in clinical trials studying Retinal Diseases
Total 3 results
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Mark Seamone, Dr.Seen in:
- Alberta, Edmonton, University of Alberta
Trials:- NCT04855045 (Principal Investigator)
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Nancy E Braverman, MD, MSSeen in:
- Quebec, Montreal, Frederique Arnaud
- Quebec, Montreal, Research Institute of the McGill University Health Center
Trials:- NCT01668186 (Principal Investigator)
- NCT06190626 (Principal Investigator)
Conditions:- Peroxisome Biogenesis Disorder;
- Zellweger Spectrum Disorder;
- RCDP - Rhizomelic Chondrodysplasia Punctata;
- D-Bifunctional Protein Deficiency;
- Alpha-Methylacyl-CoA Racemase Deficiency;
- Peroxisomal Acyl-CoA Oxidase Deficiency;
- Peroxisomal Acyl-CoA Oxidase 2 Deficiency;
- ATP Binding Cassette Subfamily D Member 3 Gene Mutation;
- ACBD5 (AcylCoA Binding Domain 5) Deficiency;
- Adult Refsum Disease;
- Sterol Carrier Protein 2 Deficiency
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Sonja Karst, MDSeen in:
- Vancouver, Eye Care Center
Trials:- NCT03765112 (Sub-Investigator)
Conditions:
Clinical Trials on Retinal Diseases
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Shanghai General Hospital, Shanghai Jiao Tong University...RecruitingInherited Retinal DystrophiesChina
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Samsung Medical CenterCompletedRetinal Detachment | Retinal Break
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Gangnam Severance HospitalCompletedInherited Retinal Dystrophy Primarily Involving Sensory Retina | Inherited Retinal Dystrophy Primarily Involving Retinal Pigment EpitheliumKorea, Republic of
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Fondation Ophtalmologique Adolphe de RothschildRecruitingHereditary Retinal DystrophiesFrance
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Innostellar Biotherapeutics Co.,LtdRecruitingInherited Retinal DystrophyChina
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Duke UniversityRecruitingRetinal DystrophiesUnited States
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Benha UniversityUnknownDystrophy, RetinalUnited Arab Emirates
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University Hospital, MontpellierInstitut National de la Santé Et de la Recherche Médicale, FranceRecruiting
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Frontera TherapeuticsRecruitingBiallelic RPE65 Mutation-associated Retinal DystrophyChina
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PYC TherapeuticsRecruitingRetinal Dystrophy | PRPF31 Mutationassociated Retinal Dystrophy | RP11United States