A Study of MT-4561 in Patients With Various Advanced Solid Tumors
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Tanabe Pharma America, Inc.
- Study ID
- NCT06943521
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
- Biliary Tract Cancer
- Breast Cancer
- Cervical Cancer
- Endometrial Cancer
- Esophageal Cancer
- Gastric Cancer
- Head and Neck Squamous Cell Carcinoma (HNSCC)
- Neuroendocrine Carcinoma (NEC)
- Neuroendocrine Tumor (NET)
- Non-small Cell Lung Cancer (NSCLC)
- Nuclear Protein in Testis (NUT) Carcinoma
- Ovarian Cancer
- Pancreatic Ductal Adenocarcinoma (PDAC)
- Prostate Cancer
- Soft Tissue Sarcoma
- Urothelial Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- MT-4561 — DRUGi.v.
Study Details
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.
Key Dates
- Start date
- Apr 18, 2025
- Status verified
- Dec 2025
- Primary completion
- Aug 31, 2028
- Completion
- Aug 31, 2028
Study Design
- Enrollment
- 27 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Part 1 (Dose-escalation)Intravenous (IV) infusion of MT-4561 once every week in 28-day cycle, until disease progression or discontinuation criteria are met.
Primary Outcome Measure
Incidence of Adverse Event, Dose limiting toxicities (DLTs) [ Time Frame: a 28-day cycle ]
Central Contacts
- Clinical Trials Information Desk, to prevent miscommunication,Please E-mail
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Southern California | Los Angeles | California | 90033 | - |
| START Midwest | Grand Rapids | Michigan | 49546 | - |
| The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive Cancer Center | Columbus | Ohio | 43210 | - |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | - |
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