Helixmith announces topline results from Phase 2A ALS study
Engensis high dose with repeated treatments is safe and well-tolerated. Primary safety endpoint achieved; no serious adverse events related to drug.
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Gene therapy and biopharmaceutical contract research and manufacturing company
helixmith.comLast updated
In short: Helixmith secured government funding, started a new gene therapy trial, and saw shares rise on profit hopes.
Engensis high dose with repeated treatments is safe and well-tolerated. Primary safety endpoint achieved; no serious adverse events related to drug.
TADIOS proved safe and well-tolerated. IL-1RA levels decreased significantly, fatigue improved versus placebo. Study involved 100 subjects in India.
The agreement, signed on April 27, 2022, at GI Cell's headquarters, focuses on joint research, development, manufacturing, and commercialization of cell and gene therapy products.
VM507 activates c-Met, shows efficacy in kidney diseases. Clinical trials planned for 2023. Potential for ischemic and neurodegenerative treatments.
23-02-06 Helixmith Co., Ltd announced that it expects to receive KRW 19.999986156 billion in funding from CANARIABIO M Inc. CI 22-12-28 Helixmith Co., Ltd announced...
The head of the United Arab Emirates' pharmaceutical regulator visited Biosolution and Helixmith's research center in Seoul to discuss regulatory cooperation and potential market entry...
Helixmith, led by CEO Jang Song-seon, is moving to secure a next-generation "smart manufacturing process" for cell and gene therapies (CGT) by integra...
Another blow to Korean bio market after SillaJen's halted Pexa-Vec trials in Aug. Helixmith shares on Korea's secondary bourse Kosdaq closed 30 percent lower at...
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