This will be a Phase 1b, first in human, open-label, dose escalation and expansion study of MT-5111 (a recombinant fusion protein) given as monotherapy in subjects with HER2-positive solid tumors
This study will be conducted in two parts: Part A (Dose Escalation): The purpose of Part A is to determine the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D). Part A will include any type of HER2-positive solid cancer. Part B (Dose Expansion): The purpose of Part B is to confirm the safety and tolerability of MT-5111 doses selected from those explored in Part A including the MTD or RP2D. Part B will include 3 types of HER2-positive solid cancers in the following 3 expansion groups: Group B1: Breast cancer; Group B2: gastric or gastroesophageal adenocarcinomas (GEA); and Group B3: Other HER2-positive solid cancers. The Breast Cancer cohort will start enrolling in parallel to Part A. Up to 178 eligible subjects will be identified and treated through competitive enrollment at multiple study centers globally In Parts A and B of the study, a subject may participate for the following four periods: Screening (up to 28 days before first dose of MT-5111) Treatment period (active period where a subject will receive three weekly doses of MT-5111 over a 21-day treatment cycle) Short-term Follow-up (30 days after last dose of MT-5111) Long-term follow-up (up to 24 months after the last dose of MT-5111) MT-5111 will be given as an intravenous (IV) infusion over about 30 minutes on the same day every week (i.e., on day 1, day 8 and day 15 of each cycle, a cycle being defined as 21 days). A subject can continue receiving MT-5111 as long as it is well-tolerated, their disease has not worsened, or until the subject decides they no longer want to participate in the study.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Experimental treatment with MT-5111
To evaluate safety and determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D)
Evaluation of safety of MT-5111 as measured by number of subjects with adverse events using Common Terminology Criteria for Adverse Events (CTCAE) v 5.0
Time frame: 21 day cycle
To evaluate tolerability and determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D)
Evaluation of tolerability of MT-5111 as measured by number of subjects with dose limiting toxicities (DLTs)
Time frame: 21 day cycle
PK as measured by concentrations of free MT-5111 (Maximum Plasma Concentration [Cmax])
Evaluation of the pharmacokinetic profile of MT-5111
Time frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle
PK as measured by concentrations of free MT-5111 (Time to reach maximum concentration after drug administration [Tmax])
Evaluation of the pharmacokinetic profile of MT-5111
Time frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle
PK as measured by concentrations of free MT-5111 (Area Under the Curve [AUC])
Evaluation of the pharmacokinetic profile of MT-5111
Time frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle
To evaluate the tumor response to MT-5111
Objective response rate (ORR) defined as the proportion of subjects with either a complete response or a partial response as determined by investigator assessment
Time frame: Screening, approximately every 6 weeks, at End of Treatment and 30 days after the last dose
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Mayo Clinic (Arizona)
Phoenix, Arizona, United States
St. Joseph Heritage Healthcare
Fullerton, California, United States
Cancer and Blood Specialty Clinic
Los Alamitos, California, United States
Cedars-Sinai Medical Center
Santa Monica, California, United States
UCLA Hematology & Oncology
Santa Monica, California, United States
Sarah Cannon Research Institute
Denver, Colorado, United States
Sylvester Comprehensive Cancer Center (University of Miami)
Coral Gables, Florida, United States
South Broward Hospital District d/b/a Memorial Healthcare System
Hollywood, Florida, United States
Mayo Clinic (Florida)
Jacksonville, Florida, United States
Orlando Health
Orlando, Florida, United States
...and 20 more locations
To evaluate the immunogenicity of MT-5111
Immunogenicity as measured by MT-5111 (anti-drug antibody \[ADA\] titer)
Time frame: Screening (baseline), Day 1 of each 21 day cycle, at the End of Treatment and the Follow-up Visit
To evaluate the immunogenicity of MT-5111
Immunogenicity as measured by MT-5111 (neutralizing antibody \[NAb\])
Time frame: Screening (baseline), Day 1 of each 21 day cycle, at the End of Treatment and the Follow-up Visit