Receives FDA authorization to initiate ELEVATE-44-102, a Phase 1b multiple ascending dose clinical study of ENTR-601-44 in adults living with ...

Entrada Therapeutics (TRDA) announced that the United States Food and Drug Administration has lifted the clinical hold on ENTR-601-44 and ...

Entrada Therapeutics gains FDA clearance for its Phase 1b ELEVATE-44-102 study, evaluating ENTR-601-44 in adult Duchenne ...

Receives FDA authorization to initiate ELEVATE-44-102, a Phase 1b multiple ascending dose clinical study of ENTR-601-44 in adults living with Duchenne muscular dystrophy - - Follows recently received ...

Entrada Therapeutics is finally able to get its Duchenne muscular dystrophy candidate (DMD) back on track after the FDA ...

波士顿 - 根据 InvestingPro 数据显示，市值4.76亿美元且财务状况良好的生物科技公司Entrada Therapeutics, Inc. (NASDAQ: TRDA )已获得美国食品和药物管理局（FDA）批准，可以开展其杜氏肌营养不良症（DMD）实验性治疗药物ENTR-601-44的1b期临床试验。此前，英国药品和保健品监管局也批准了相关研究。

Shares of Entrada Therapeutics rose after regulators removed a clinical hold and said its lead product candidate could be studied as a treatment for Duchenne muscular dystrophy. The stock was up 9.5% ...

Phase 1b US study planned for 2026, as company competes with NS Pharma and Avidity Biosciences in exon 44 space ...

Interested parties may access the live and archived webcasts under the "Investors” section of the company's website at: https ...

Q: How does 10-301 differ from 10-601? A: Undergraduates must register for 10-301 and graduate students must register for 10-601. Otherwise, the courses will be identical in all respects. A: This is ...