Product Description
For Advanced Retinitis Pigmentosa (Sourced from: https://clinicaltrials.gov/ct2/show/NCT00458575)
Mechanisms of Action: Cell Therapy
Novel Mechanism: No
Modality: Cell Therapy
Route of Administration: Injection
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Johnson & Johnson
Company Location: NEW BRUNSWICK NJ 08933
Company CEO: Joaquin Duato
Additonal Commercial Interests: None
Clinical Description

Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 2: Macular Degeneration|Geographic Atrophy
Phase 1: Retinitis Pigmentosa
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
CR108188 | P2 |
Withdrawn |
Macular Degeneration|Geographic Atrophy |
2021-02-20 |
|
JapicCTI-163414 | P2 |
Terminated |
Geographic Atrophy|Macular Degeneration |
2021-02-20 |
|
PRELUDE | P2 |
Completed |
Macular Degeneration|Geographic Atrophy |
2019-06-05 |
23% |
CR017548 | P2 |
Completed |
Geographic Atrophy|Macular Degeneration |
2015-03-31 |