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LTRN US Equity

Lantern Pharma Inc.Health Care · Pharmaceutical Preparations · CIK 1763950 · FY ends Dec 31
$2.49
-0.03 (-1.19%)
USD · as of 2026-08-19 · marketstack
3 registered studies · 3 active

Studies where LTRN is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

3 interventional

Held by 4 tracked-famous managers (RENAISSANCE TECHNOLOGIES LLC, CITADEL ADVISORS LLC, SUSQUEHANNA INTERNATIONAL GROUP, LLP, MARSHALL WACE, LLP) · FINRA short interest 10.1 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Safety, Pharmacokinetics, and Clinical Activity of LP-284 in Adult Patients With Relapsed or Refractory Lymphomas and Solid TumorsNCT06132503Phase 1a: To evaluate the safety and tolerability of escalating doses of LP-284Open-label · TreatmentPhase 1RecruitingDrug: LP-284Relapsed or Refractory Lymphomas, Advanced Solid Tumor1102028-11-30in 833 d2026-05-04
A Study of LP-300 With Carboplatin and Pemetrexed in Never Smokers With Advanced Lung AdenocarcinomaNCT05456256Progression-free survival (PFS)Randomized · Open-label · TreatmentPhase 2RecruitingDrug: LP-300, Pemetrexed, CarboplatinAdenocarcinoma of Lung, Carcinoma, Non-Small-Cell Lung90Dec 2026≤ 133 d2026-05-04
Study of LP-184 in Patients With Advanced Solid TumorsNCT05933265To evaluate the safety and tolerability of LP-184 assessed by the incidence and severity of all adverse events graded by CTCAE v5.0Non-randomized · Open-label · TreatmentPhase 1/2Active, not recruitingDrug: LP-184, Olaparib, Nivolumab & IpilimumabAdvanced Solid Tumor, Metastatic Solid Tumor, GBM, TNBC - Triple-Negative Breast Cancer, NSCLC, Pancreatic Adenocarcinoma, DDR Gene Mutation642026-07-282026-05-04

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19