Lantern Pharma reported Q3 2024 financial results and clinical updates, including an 86% clinical benefit rate in the LP-300 Harmonic™ Trial's initial cohort, expansion to Japan and Taiwan, and ongoing Phase 1 trials for LP-184 and LP-284 with no dose-limiting toxicities. LP-184 received FDA Fast Track Designation for Glioblastoma. Financial highlights include $28.1 million in cash and equivalents, R&D expenses of $3.7 million, and a net loss of $4.5 million ($0.42 per share). The company maintains three active clinical trials and advances AI-guided precision-oncology drug candidates.