FDA convenes advisory panel to review BrainStorm's ALS therapy NurOwn

TL;DR Summary
BrainStorm Cell Therapeutics' ALS treatment, NurOwn, will be discussed in an FDA advisory committee meeting after receiving a refusal to file letter in November. Ionis and AstraZeneca's rare disease drug, eplontersen, has completed a positive Phase III trial. Codiak BioSciences has filed for Chapter 11 bankruptcy. ArriVent Biopharma has raised $155 million in a Series B round. Endpoints has added three new journalists to their newsroom. Kristen Hege, a cancer researcher, has put her career on hold to hike the Pacific Crest Trail. Another biotech startup has faced a Phase II pileup in Parkinson's disease.
- BrainStorm gets FDA adcomm for ALS drug after failed trial and RTF Endpoints News
- Under protest, FDA to convene advisory panel to review controversial cell therapy for ALS STAT
- BrainStorm Cell Therapeutics Announces FDA Advisory Committee Meeting to Review Biologics License Application for NurOwn® for the Treatment of ALS Yahoo Finance
- BrainStorm Secures FDA Adcomm for ALS Therapy NurOwn BioSpace
- BrainStorm Announces FDA AdComm Meeting for NurOwn Stromal Cell Therapy Neurology Live
- View Full Coverage on Google News
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