Improvement in vision in intermediate dry AMD demonstrated in LIGHTSITE III trial data
June 26th 2022LumiThera Inc. noted that the trial results demonstrated statistically significant improvement in the prespecified primary endpoint in BCVA at 13 months in the PBM treatment group over the sham-treatment group.
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Permanent J-code granted for triamcinolone acetonide injectable suspension from Bausch + Lomb
June 22nd 2022The U.S. Centers for Medicare and Medicaid Services code is effective July 1 and will enhance access to Xipere, the only therapy available in the United States for suprachoroidal use in the treatment of macular edema associated with uveitis.
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Key discovery: Humanin G reduces protein levels of inflammation markers associated with AMD
June 8th 2022According to the study by a team of researchers from the University of California Irvine and University of Southern California, treatment with Humanin G reduced protein levels of inflammation markers that become elevated in age-related macular degeneration.
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New drug application filed for pegcetacoplan for the treatment of geographic atrophy
June 1st 2022The company noted that pegcetacoplan, designed to regulate excessive activation of the complement cascade, part of the body’s immune system, which can lead to the onset and progression of many serious diseases, was granted Fast Track designation by the FDA for the treatment of geographic atrophy.
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The American Academy of Ophthalmology applauded Congress for reaching the 290-consponsor milestone for the proposal. By reaching the two-thirds majority of bipartisan support in Congress, the bill is eligible for inclusion on the Consensus Calendar under new rules that were established in 2019.
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Phase 2 INTEGRAL trial: THR-689 fails to meet primary endpoints in eyes with DME, will not advance
May 10th 2022According to the company, the trial did not demonstrate efficacy on the key clinical endpoints. As a result, Oxurion will now shift its focus to the Phase 2 development program for THR-149, which recently demonstrated a compelling safety and efficacy profile for the treatment of DME.
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