Phase 1 dose-escalation study of a siRNA targeting the RTP801 gene in age-related macular degeneration patients

Aged, 80 and over Male 0301 basic medicine Dose-Response Relationship, Drug Maximum Tolerated Dose Microscopy, Acoustic Biological Availability Choroidal Neovascularization 3. Good health Macular Degeneration 03 medical and health sciences Area Under Curve Intravitreal Injections Humans Female RNA Interference Prospective Studies RNA, Small Interfering Tomography, Optical Coherence Aged Half-Life RNA, Double-Stranded Transcription Factors
DOI: 10.1038/eye.2012.106 Publication Date: 2012-05-25T09:43:22Z
ABSTRACT
To evaluate the safety, tolerability, pharmacokinetics, and dose-limiting toxicities of a single intravitreal (IVT) injection of PF-04523655, a 19-nucleotide, O-methyl stabilized, double-stranded small interfering ribonucleic acid targeting the RTP801 gene in patients with neovascular age-related macular degeneration (AMD).Prospective, phase 1, clinical multicentre trial, enrolled 27 patients with neovascular AMD unresponsive to prior treatment and best corrected visual acuity (BCVA) ≤ 20/200 in the study eye in stratum 1: (dose-escalating, open-label: 50 to 3000 μg of PF-04523655) and 27 patients who had potential to benefit from therapy and BCVA of ≤ 20/100 and ≥ 20/800 in stratum 2 (parallel, masked study of 1000, 1500, 2250, and 3000 μg of PF-04523655). The primary outcome was safety and tolerability assessment as well as pharmacokinetic profiling following a single IVT injection of PF-04523655.Doses of PF-04523655 ≥ 400 μg were generally detectable in the plasma at 1, 4, and 24 h post-injection. And all doses were below the lowest level of quantification by day 14. A single IVT injection of 50 to 3000 μg of PF-045237655 was generally safe and well tolerated over 24 months. There were no dose-limiting toxicities.A single IVT injection of PF-0523655 ≤ 3000 μg seems safe and well tolerated in eyes with neovascular AMD.
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