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LumiThera, Inc Announces Completion of Diopsys, Inc Acquisition

/PRNewswire/ LumiThera Inc., a commercial stage medical device company offering photobiomodulation (PBM) treatment for ocular damage and disease, today.

United statesClarke tedfordJoe fontanettaDiopsys incEuropean unionFood drug administrationLumithera incPrnewswire lumithera incThera incLight delivery systemAge related macular degenerationSouth americanVisual evoked potentialTesting systemValeda light delivery systemDrug administration

LumiThera Inc : LumiThera, Inc Announces Completion of Diopsys, Inc Acquisition

SEATTLE, March 3, 2022 /PRNewswire/ LumiThera Inc., a commercial stage medical device company offering photobiomodulation (PBM) treatment for ocular damage and disease, today announced the

United statesClarke tedfordKostenloser wertpapierhandelJoe fontanettaDiopsys incEuropean unionFood drug administrationLumithera incPrnewswire lumithera incThera incDelivery systemAge related macular degenerationSouth americanVisual evoked potentialTesting systemLight delivery system

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LumiThera Announces Top Line Data in the European Multi-Center, LIGHTSITE II Clinical Study to Treat Dry Age-Related Macular Degeneration

Press release content from PR Newswire. The AP news staff was not involved in its creation. LumiThera Announces Top Line Data in the European Multi-Center, LIGHTSITE II Clinical Study to Treat Dry Age-Related Macular Degeneration April 7, 2021 GMT SEATTLE, April 7, 2021 /PRNewswire/ LumiThera Inc., a commercial stage medical device company delivering photobiomodulation (PBM) treatment for ocular disorders and disease, today announced positive findings in its LIGHTSITE II, multi-center clinical trial in dry Age-Related Macular Degeneration (AMD) patients. The prospective, double-masked, randomized, multi-center, European Union post-marketing clinical trial, titled LIGHTSITE II, was conducted in eight leading retinal centers based in the United Kingdom, Germany, Spain, Italy and France. The objective was to treat dry AMD subjects over the course of three rounds of PBM sessions every four months with a duration of 10 months. The study was converted to a smaller pilot as some of th

Comunidad autonoma de catalunaUnited statesUnited kingdomSchleswig holsteinClark tedfordMarion munkBen burtonJames paget university hospitalEuropean unionFood drug administrationBern photographic reading centerPrnewswire lumithera incLumithera incThera incAge related macular degenerationMedical director

LumiThera Announces Positive Interim Data in Visual and ERG Clinical Outcomes in the ELECTROLIGHT Pilot Study in Dry AMD patients

(1) SEATTLE, Feb. 16, 2021 /PRNewswire/ LumiThera Inc., a commercial stage medical device company offering a photobiomodulation (PBM) treatment for ocular damage and disease, today announced the interim data from the ELECTROLIGHT pilot study in dry AMD patients. A total of 23 eyes from 15 subjects with intermediate Dry AMD were enrolled into the prospective clinical study and treated with PBM using the Valeda Light Delivery System (3 times per week for 3 weeks). Subjects were tested for safety and functional vision improvements using the Diopsys electroretinogram (ERG) device. ERG is a diagnostic test that measures the electrical activity of the retina of the eye in response to a light stimulus. All subjects were tested at weekly intervals for ERG function prior to the start of the next week of PBM treatments. An interim analysis was performed following the Month 1 study visit. The study was conducted by Dan Montzka, M.D. and Larry Perich, D.O. at the Perich Eye Center (New Por

United statesLarry perichKostenloser wertpapierhandelDan montzkaPerich eye center new port richeyDiopsys incEuropean unionFood drug administrationPrnewswire lumithera incLumithera incThera incDelivery systemPerich eye centerNew port richeyVisual evoked potentialTesting system