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Study of MT-5111 in HER2-positive Solid Tumors (MT-5111)

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ClinicalTrials.gov Identifier: NCT04029922
Recruitment Status : Recruiting
First Posted : July 23, 2019
Last Update Posted : July 7, 2022
Sponsor:
Information provided by (Responsible Party):
Molecular Templates, Inc.

Study Description
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Brief Summary:
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

Condition or disease Intervention/treatment Phase
HER2-positive Solid Cancers Drug: MT-5111 (experimental study drug) Phase 1

Detailed Description:

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 Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 178 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: MT-5111 (active drug)
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1 Open-label, Multicenter Dose Escalation and Expansion Study of MT-5111 in Subjects With Previously Treated Advanced HER2-positive Solid Tumors
Actual Study Start Date : November 12, 2019
Estimated Primary Completion Date : May 2023
Estimated Study Completion Date : May 2025
Arms and Interventions
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Arm Intervention/treatment
Experimental: Part A- Dose Escalation

Part A- Dose Escalation in patients with previously treated advanced HER2-positive solid tumors.

The assigned dose level of 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).

 Drug: MT-5111 (experimental study drug)
Experimental treatment with MT-5111
Experimental: Part B- Dose Expansion

Part B - Dose Expansion in previously treated HER2-positive breast, GEA and other HER2-positive solid cancers

Part B will include 3 expansion groups: Group B1 (Breast Cancer) will begin enrolling while Part A is being conducted following the completion of Cohort 7 and Subsequent cohort of subjects in group B1 may enroll into higher doses that are tolerated in Part A. Group B2 (GEA) and Group B3 (Other HER-2 positive solid cancer groups) will begin enrollment after the MTD or RP2D is determined in Part A.

The assigned dose level of 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).

 Drug: MT-5111 (experimental study drug)
Experimental treatment with MT-5111


Outcome Measures
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Primary Outcome Measures :
  1. To evaluate safety and determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) [ Time Frame: 21 day cycle ]
    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

  2. To evaluate tolerability and determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) [ Time Frame: 21 day cycle ]
    Evaluation of tolerability of MT-5111 as measured by number of subjects with dose limiting toxicities (DLTs)


Secondary Outcome Measures :
  1. PK as measured by concentrations of free MT-5111 (Maximum Plasma Concentration [Cmax]) [ Time Frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle ]
    Evaluation of the pharmacokinetic profile of MT-5111

  2. PK as measured by concentrations of free MT-5111 (Time to reach maximum concentration after drug administration [Tmax]) [ Time Frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle ]
    Evaluation of the pharmacokinetic profile of MT-5111

  3. PK as measured by concentrations of free MT-5111 (Area Under the Curve [AUC]) [ Time Frame: Day 1, Day 8, and Day 15 in Each 21-Day cycle ]
    Evaluation of the pharmacokinetic profile of MT-5111

  4. To evaluate the tumor response to MT-5111 [ Time Frame: Screening, approximately every 6 weeks, at End of Treatment and 30 days after the last dose ]
    Objective response rate (ORR) defined as the proportion of subjects with either a complete response or a partial response as determined by investigator assessment

  5. To evaluate the immunogenicity of MT-5111 [ Time Frame: Screening (baseline), Day 1 of each 21 day cycle, at the End of Treatment and the Follow-up Visit ]
    Immunogenicity as measured by MT-5111 (anti-drug antibody [ADA] titer)

  6. To evaluate the immunogenicity of MT-5111 [ Time Frame: Screening (baseline), Day 1 of each 21 day cycle, at the End of Treatment and the Follow-up Visit ]
    Immunogenicity as measured by MT-5111 (neutralizing antibody [NAb])


Other Outcome Measures:
  1. To correlate the pharmacodynamic markers of cancer under study (for breast cancer subjects using historic data, if available) [ Time Frame: Screening (baseline) ]
    The expression of HER2, Estrogen Receptor (ER), Progesterone Receptor (PgR) and Ki67 (exploratory) on the tumor cell analyzed by immunohistochemistry

  2. To correlate the pharmacodynamic markers of cancer under study relationship for MT-5111 using the PK, pharmacodynamics, safety, and tumor response variables. [ Time Frame: Screening (baseline), every 6 weeks (± 1 week) and within 7 days of the EoT Visit. ]
    Serum-HER2 (s-HER2)

  3. If warranted by the study results, to evaluate the exposure-response relationship for MT-5111 [ Time Frame: Screening (baseline), every 6 weeks (± 1 week) and within 7 days of the EoT Visit. ]
    Analyze data collected for all primary, secondary and exploratory endpoints using the PK, pharmacodynamics, safety, and tumor response variables

  4. To evaluate overall Survival [ Time Frame: 30 days after last dose, and every 3 months for up to 24 months ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Histologically confirmed, unresectable, locally advanced or metastatic solid cancers:

    • Part A (Dose-Escalation): All HER2-positive solid cancers are eligible
    • Part B (Dose-Expansion): Any type of HER2-positive solid cancer, including breast cancer, and gastric or gastroesophageal adenocarcinomas (GEA).
  2. HER2-positive in the latest tumor sample tested for HER2 (testing to be done on a metastatic lesion in cases of metastatic cancers).
  3. Relapsed or refractory to or intolerant of existing therapy(ies)
  4. At least 1 measurable or evaluable lesion according to RECIST 1.1 (Subjects with evaluable disease only may be included in the dose escalation phase)
  5. ECOG performance score of ≤ 1

  6. Adequate Bone marrow function as determined by:

    • Absolute neutrophil count (ANC) ≥ 1,000/mm3
    • Platelet count ≥ 75,000 mm³ and
    • Hemoglobin ≥ 8.0 g/dL
    • Red blood cell transfusion within 2 weeks of study treatment start is allowed if hemoglobin levels remain stable

  7. Kidney function:

    • Creatinine clearance (CLcr) ≥ 50 mL/min either measured or estimated using the Cockcroft-Gault formula

  8. Cardiac Function:

    • Left ventricular ejection fraction (LVEF) ≥ 55% on the echocardiogram (ECHO) assessment (preferred), or multigated acquisition (MUGA) scan, and QTcF ≤ 480 ms for women and QTcF ≤ 450 ms for men [average from three QTcF values on the triplicate 12-lead electrocardiogram (ECG)] at baseline

  9. Hepatic function:

    • Total bilirubin ≤ 1.5 x ULN, or ≤ 3 x ULN for subjects with Gilbert's Syndrome and
    • AST ≤ 3 x ULN (or ≤ 5 x ULN if liver metastasis) and ALT ≤ 3 x ULN (or ≤ 5 x ULN if liver metastasis)

Exclusion Criteria:

  1. History or current evidence of another tumor that is histologically distinct from the tumor under study

  2. Current evidence of new or growing CNS metastases during screening

    • Subjects with known CNS metastases will be eligible if they meet protocol specified criteria
  3. Evidence of CTCAE Grade >1 toxicity before the start of treatment, except for hair loss and those Grade 2 toxicities listed as permitted in other eligibility criteria
  4. History or evidence of significant cardiovascular disease
  5. Current evidence of active, uncontrolled hepatitis B virus, hepatitis C virus, human immunodeficiency virus (HIV) (evidenced by detectable viral load by PCR) or acquired immunodeficiency syndrome (AIDS) related illness
  6. Current evidence of ≥ grade 2 underlying pulmonary disease
  7. Certain exclusionary prior treatments
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04029922


Contacts
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Contact: Joshua Pelham (415) 378-4738 joshua.pelham@mtem.com
Contact: Amanda Keaton 859-354-7222 Amanda.Keaton@mtem.com

Locations
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Sponsors and Collaborators
Molecular Templates, Inc.
More Information
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Responsible Party: Molecular Templates, Inc.
ClinicalTrials.gov Identifier: NCT04029922    
Other Study ID Numbers: MT-5111_001
First Posted: July 23, 2019    Key Record Dates
Last Update Posted: July 7, 2022
Last Verified: July 2022

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No