Condition: Relapsed or Refractory Lymphomas · Advanced Solid Tumor · Sponsor: Lantern Pharma Inc.
The goal of this clinical trial is to evaluate the safety and tolerability of escalating doses of LP-284 and to determine the maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) in patients with relapsed or refractory (R/R) lymphomas and solid tumors. The secondary objectives are to characterize the pharmacokinetics (PK) of LP-284 and to assess clinical activity of LP-284.
This description comes directly from the study's public registry record.
Sandra Sinclair, BSBA, MHA/Ed, RN · 832-622-1699 · sandra@lanternpharma.com
Always discuss trial participation with your own doctor first.
| START Mountain Region | West Valley City, Utah, United States | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06132503