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

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Patients who have failed at least 1 prior therapy and, who have no standard treatment options demonstrated to provide clinical benefit or who are intolerable to or refuse further standard therapies will be enrolled.

• Male or female patient aged 18 years or older at the time of signing the informed consent form

• ≥ 1 measurable lesion by the RECIST v1.1

• Eastern Cooperative Oncology Group (ECOG) performance status: 0 to 1

• Life expectancy of at least 3 months

• Adequate bone marrow function

• Adequate hepatic function

• Adequate renal function estimated creatinine clearance ≥ 60 mL/min calculated using the Cockcroft and Gault equation or by institutional method

• Part 1: Patients must have a confirmed histologic or cytologic diagnosis of one of the following solid tumors for participation in the study: head and neck squamous cell carcinoma (HNSCC), non-small cell lung cancer (NSCLC), esophageal cancer, gastric cancer, biliary tract cancer, pancreatic ductal adenocarcinoma (PDAC), breast cancer, ovarian cancer, cervical cancer, endometrial cancer, prostate cancer, urothelial carcinoma, neuroendocrine tumor (NET) or neuroendocrine carcinoma (NEC), soft tissue sarcoma, and NUT carcinoma.

Locations
United States
California
University of Southern California
RECRUITING
Los Angeles
Michigan
START Midwest
RECRUITING
Grand Rapids
Ohio
The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive Cancer Center
RECRUITING
Columbus
Texas
The University of Texas MD Anderson Cancer Center
RECRUITING
Houston
Other Locations
Japan
National Cancer Center Hospital
RECRUITING
Chuo-ku
National Cancer Center Hospital East
RECRUITING
City
Contact Information
Primary
Clinical Trials Information Desk, to prevent miscommunication,
information@mt-pharma-us.com
Please E-mail
Time Frame
Start Date: 2025-04-18
Estimated Completion Date: 2028-08
Participants
Target number of participants: 27
Treatments
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.
Sponsors
Leads: Mitsubishi Tanabe Pharma America Inc.

This content was sourced from clinicaltrials.gov

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