Blindness: Clinical Trials

6 trials for Blindness, newest first

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6 terminated. 6 Phase 2, 2 Phase 1, 2 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 26Terminated 6
Phase 12Terminated 2
Phase 32Terminated 2

Follow Blindness: new trials by email Literature Review of Blindness trials Research Report on Blindness

Trials (filtered) newest first · largest first

All 6 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Study to Evaluate the Efficacy Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene With Early to Moderate Vision Loss (Celeste)
QR-421a, Sham-procedure - Retinitis Pigmentosa, Usher Syndrome Type 2
Phase 2 / Phase 3TerminatedLaboratoires Thea52021-12-152024-08-07
Study to Evaluate the Efficacy Safety and Tolerability of Ultevursen in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene (Sirius)
Ultevursen, Sham-procedure - Retinitis Pigmentosa, Usher Syndrome Type 2
Phase 2 / Phase 3TerminatedLaboratoires Thea72021-12-082024-07-12
An Open-Label Extension Study to Evaluate Safety & Tolerability of QR-421a in Subjects With Retinitis Pigmentosa
RNA antisense oligonucleotide for intravitreal injection - Retinitis Pigmentosa, Usher Syndrome Type 2
Phase 2TerminatedLaboratoires Thea212021-09-162024-08-07
Extension Study to Study PQ-110-001 (NCT03140969)
QR-110 - Leber Congenital Amaurosis 10, Blindness
Phase 1 / Phase 2TerminatedLaboratoires Thea92019-05-132024-10-15
Fluoxetine for Visual Recovery After Ischemic Stroke
Fluoxetine, Placebo - Acute Stroke, Visual Field Loss
Phase 2TerminatedBogachan Sahin172016-05-012021-10-13
Study of SAR421869 in Participants With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B
SAR421869 - Usher Syndrome, Retinitis Pigmentosa
Phase 1 / Phase 2TerminatedSanofi92012-03-262022-04-28

Narrower conditions

Eye Diseases (4)  ·  Retinal Diseases (4)  ·  Retinitis Pigmentosa (4)  ·  Usher Syndromes (4)  ·  Vision Disorders (4)  ·  Eye Abnormalities (3)  ·  Eye Diseases, Hereditary (3)  ·  Genetic Diseases, Inborn (1)  ·  Hemianopsia (1)  ·  Ischemic Stroke (1)  ·  Leber Congenital Amaurosis (1)  ·  Leber Congenital Amaurosis 10 (1)  ·  Meckel Syndrome, Type 4 (1)  ·  Neurologic Manifestations (1)

Broader conditions

Nervous System Diseases (6)  ·  Pathological Conditions, Signs and Symptoms (6)  ·  Signs and Symptoms (6)  ·  Congenital Abnormalities (5)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5)  ·  Neurologic Manifestations (5)  ·  Sensation Disorders (5)  ·  Abnormalities, Multiple (4)  ·  Deaf-Blind Disorders (4)  ·  Deafness (4)  ·  Ear Diseases (4)  ·  Genetic Diseases, Inborn (4)  ·  Hearing Disorders (4)  ·  Hearing Loss (4)

Interventions

Intravitreal Injections (3)  ·  Fluoxetine (1)

Sponsors

Laboratoires Thea (4)  ·  Bogachan Sahin (1)  ·  Sanofi (1)

Countries

United States (6)  ·  France (2)  ·  United Kingdom (2)  ·  Belgium (1)  ·  Canada (1)  ·  Germany (1)  ·  Netherlands (1)

Top investigators

Jose-Alain Sahel, MD, PhD (1)  ·  Richard Weleber, MD (1)

Results publications

PMID 24705452, PMID 33230035, PMID 36166771

NIH funding

2018 (1)