Lantern Pharma (NASDAQ: LTRN) a clinical-stage AI-driven precision oncology company, reported first-quarter 2026 operational highlights and financial results, highlighting a 47% year-over-year reduction in research and development spending while advancing multiple clinical programs through key regulatory milestones, including a successful FDA Type C meeting outcome for the Phase 2 HARMONIC trial of LP-300 and IND clearance for Starlight Therapeutics’ first pediatric CNS cancer program. The company also launched withZeta.ai, its multi-agentic AI drug development platform, outlined plans to separate its AI assets into an independent entity, and said recent financing of up to $9.25 million extends its operating runway into the first quarter of 2027.
To view the full press release, visit https://ibn.fm/R1C54
About Lantern Pharma Inc.
Lantern Pharma Inc. (NASDAQ: LTRN) is a clinical-stage precision oncology company leveraging AI, machine learning, and its proprietary RADR(R) platform to transform the development of cancer therapies. Lantern’s clinical pipeline includes LP-184 (acylfulvene), LP-284 (a TC-NER targeting compound in hematologic and solid tumors), and LP-300 (cisplatin/ethacraplatin analog), which is being evaluated in the HARMONIC Phase 2 trial in never-smoker patients with relapsed advanced lung adenocarcinoma following TKI treatment. LP-184 is also being developed for pediatric CNS cancers through Starlight Therapeutics, Lantern’s wholly owned CNS-focused subsidiary. withZeta.ai, Lantern’s multi-agentic AI co-scientist platform, is now commercially available as a subscription-based research platform for the global biomedical and drug development community, representing a new revenue stream for the Company. Lantern operates an AI Center of Excellence in Bengaluru, India and is headquartered in Dallas, Texas.
NOTE TO INVESTORS: The latest news and updates relating to LTRN are available in the company’s newsroom at https://ibn.fm/LTRN
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