A Study of MT-4561 in Patients With Various Advanced Solid Tumors (NCT06943521)
A Phase I/II, Dose-escalation and Dose-optimization Study to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of MT-4561 in Patients With Various Advanced Solid Tumors and to Evaluate Effect of MT-4561 on Pharmacokinetics of Oral Midazolam
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a First In Human (FIH), multicenter, open-label, Phase I/II study to evaluate safety, tolerability, Pharmacokinetics (PK), pharmacodynamics, and efficacy of MT-4561 in patients with advanced solid tumors. This study will be conducted in 3 parts. Part 1 is aimed at evaluating safety, tolerability, PK and pharmacodynamics of MT-4561 and determining the Maximum Tolerated Dose (MTD) using the Bayesian Optimal Interval (BOIN) design. The study details and doses of Part 2 (dose-optimization) and Part 3 (Drug-Drug Interaction) will be available after review of applicable Part 1 results.
Who can join: Review the eligibility criteria below.
Location: University of Southern California โ Los Angeles, California
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (6 Sites)
- University of Southern California โ Los Angeles, California
- START Midwest โ Grand Rapids, Michigan
- The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive Cancer Center โ Columbus, Ohio
- The University of Texas MD Anderson Cancer Center โ Houston, Texas
- National Cancer Center Hospital โ Chuo-Ku, Tokyo
- National Cancer Center Hospital East โ City,
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Head and Neck Squamous Cell Carcinoma (HNSCC)
- SBRT +/- Pembrolizumab in Patients With Local-Regionally Recurrent or Second Primary Head and Neck Carcinoma โ Tucson, Arizona
- INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPSโฅ20 HNSCC โ Duarte, California
- Study of Safety and Tolerability of Nivolumab Treatment Alone or in Combination With Relatlimab or Ipilimumab in Head and Neck Cancer โ Pittsburgh, Pennsylvania
- [18F]-AraG PET Imaging in LA HNSCC โ Indianapolis, Indiana
- A Study to See if Giving Fianlimab and Cemiplimab Together is Better Than Cemiplimab Alone at Treating Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma โ Los Angeles, California
- Study to Assess GTAEXS617 in Participants With Advanced Solid Tumors โ Los Angeles, California
Explore by condition: All Head and Neck Squamous Cell Carcinoma (HNSCC) clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.