Jun. 25 at 11:49 AM
$NTHI We recently announced that NEO100 has received IND authorization from the Department of Health, Abu Dhabi. Why is the UAE authorization for NEO100 so significant?
The authorization spans three clinical protocols, adult studies from Phase 1 through Phase 2, and includes a defined pediatric development pathway. This broad authorization is intended to support parallel development activities as NeOnc advances its intranasal delivery platform internationally.
In the United States, NEO100 has already received FDA Orphan Drug, Fast Track, and Rare Pediatric Disease designations. The NEO100-01 Phase 2a trial in recurrent IDH1-mutant high-grade glioma is fully enrolled, and NeOnc expects to report top-line data by the end of July 2026.
The upcoming readout represents an important milestone in evaluating NEO100's potential as a non-invasive treatment approach for patients with recurrent high-grade gliomas.
Read more: https://investors.neonc.com/news-releases/news-release-details/neonc-technologies-receives-uae-ind-approval-neo100-expanding
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