Drug Type AAV based gene therapy |
Synonyms Laru-zova, Laruparetigene Zovaparvovec, Laruparetigene zovaparvovec + [3] |
Target |
Action modulators |
Mechanism RPGR modulators(X-linked retinitis pigmentosa GTPase regulator modulators) |
Therapeutic Areas |
Active Indication |
Inactive Indication- |
Originator Organization |
Active Organization |
Inactive Organization- |
License Organization |
Drug Highest PhasePhase 2/3 |
First Approval Date- |
RegulationFast Track (United States), Orphan Drug (United States), Orphan Drug (European Union), PRIME (European Union), Regenerative Medicine Advanced Therapy (United States), Priority Review (European Union), Innovative Licensing and Access Pathway (United Kingdom) |

| Indication | Highest Phase | Country/Location | Organization | Date |
|---|---|---|---|---|
| X-linked retinitis pigmentosa | Phase 3 | United States | 14 Mar 2024 | |
| X-linked retinitis pigmentosa | Phase 3 | Australia | 14 Mar 2024 | |
| X-linked retinitis pigmentosa | Phase 3 | Canada | 14 Mar 2024 | |
| X-linked retinitis pigmentosa | Phase 3 | United Kingdom | 14 Mar 2024 | |
| X-linked retinitis pigmentosa | Phase 3 | United Kingdom | 14 Mar 2024 |
Phase 2 | 11 | Laru-zova high dose | vreqmprjit(ddibqtooop) = zxtykbvxrx iikgqhiuww (jjffqfjisa, 4.89) View more | Positive | 04 May 2025 | ||
Phase 2 | - | amwxwsoqau(lthozhjgrz) = None mgcmolvgsk (gsuvmjqgay ) View more | Positive | 06 Dec 2024 | |||
Phase 2 | - | kcaczjlszq(niotfbhpvm) = ewckyixgim zkjnxhlwim (uffdabesrk ) | Positive | 15 Oct 2024 | |||
Not Applicable | - | ajzmlcdhsi(ppzliaxtgk) = No SUSARs or endophthalmitis were reported out to Month 36, and no participants early terminated due to a TEAE. Seven ocular SAEs were reported in 7 participants (retinal detachment [4], subcapsular cataract [1], glaucoma [1] and reduced visual acuity [1]). None of these were thought to be related to the investigational material. Of note, 3 of the retinal detachments occurred in periperally dosed patients. The TEAEs deemed related to AGTC-501 were all non-serious (mostly Grade 1-2 in severity), except one Grade 3 retinal depigmentation in the highest dose group which was not associated with any visual sequelae. Temporally, 73% of ocular TEAEs occurred within 3 months of AGTC-501 administration, 52% of which resolved within 1 month of onset. jscnrgxmmz (dqhpojwndh ) | - | 19 Sep 2024 | |||
Phase 1/2 | 29 | ztofmuezhr(eksyisebdj) = All non-serious (mostly Grade 1-2 in severity), except one Grade 3 retinal depigmentation frwiyipvhp (pjctarkoab ) View more | Positive | 05 Oct 2023 |





