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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05027139
Other study ID # ZWI-ZW25-204
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date September 15, 2021
Est. completion date January 31, 2025

Study information

Verified date March 2024
Source Jazz Pharmaceuticals
Contact Clinical Trial Disclosure & Transparency
Phone 215-832-3750
Email ClinicalTrialDisclosure@JazzPharma.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is being done to find out if zanidatamab when given with evorpacept (ALX148) is safe and can treat patients with advanced (locally advanced [inoperable] and/or metastatic) human epidermal growth factor receptor 2 (HER2)-expressing cancer.


Description:

Part 1 of the study will first evaluate the safety and tolerability and establish the recommended doses (RDs) of zanidatamab in combination with evorpacept (ALX148). Part 2 of the study will evaluate the anti-tumor activity of the combination of zanidatamab plus evorpacept (ALX148) at the RD levels in indication-specific expansion cohorts.


Recruitment information / eligibility

Status Recruiting
Enrollment 93
Est. completion date January 31, 2025
Est. primary completion date July 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Locally advanced (inoperable) and/or metastatic HER2-expressing cancer based on local or central laboratory test results as follows: - Parts 1 and 2: HER2-positive breast cancer as defined per American Society of Clinical Oncology (ASCO)/ College of American Pathologists (CAP) guidelines - Parts 1 and 2: HER2-low breast cancer (defined as immunohistochemistry [IHC] 1+ or IHC 2+; AND is currently not and has never been HER2-positive per the ASCO/CAP guidelines) - Part 2: HER2-positive gastroesophageal adenocarcinoma as defined per the ASCO/CAP gastric cancer-specific guidelines; or other HER2-overexpressing non-breast cancers (defined as IHC 3+; or IHC 2+ and in situ hybridization [ISH]+) per the ASCO/CAP guidelines for breast cancer - Progression after or during the most recent systemic regimen of treatment for advanced cancer. For both Part 1 and Part 2, prior therapies must have included approved agents known to confer clinical benefit. - Subjects with HER2-positive breast cancer who did not receive trastuzumab or pertuzumab due to medical contraindications will not be eligible for this study - Subjects with HER2-low breast cancer who have received prior HER2-targeted therapy (other than trastuzumab deruxtecan, which is allowed but not required) will not be eligible for this study - Measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) - Willingness to undergo a new biopsy to provide a tumor tissue for central laboratory testing of HER2 protein expression and gene amplification by IHC and ISH assays, respectively - Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 - Adequate organ functions - Adequate cardiac left ventricular function, as defined by a left ventricular ejection fraction (LVEF) = 50% as determined by either echocardiogram or multiple gated acquisition scan (MUGA) obtained within 4 weeks prior to first dose of study treatment Exclusion Criteria: - Previous allogeneic stem cell transplant - Prior treatment with any anti-CD47 or anti-signal regulatory protein alpha (SIRPa) agent - Prior or concurrent invasive malignancy whose natural history or treatment has, in the opinion of the investigator or medical monitor, the potential to interfere with the safety or efficacy assessment of the investigational regimen - Received systemic anticancer therapy within 4 weeks of starting study treatment (6 weeks for mitomycin C or nitrosoureas). Received radiotherapy within 2 weeks of the first dose of zanidatamab/evorpacept (ALX148) - Untreated brain metastases, symptomatic brain metastases; or radiation treatment (stereotactic radiosurgery and whole brain radiation) for brain metastases within 2 weeks of start of study treatment - Known leptomeningeal disease - Active hepatitis - Infection with human immunodeficiency virus (HIV)-1 or HIV-2. (Exception: Subjects with well controlled HIV [e.g., CD4 > 350/mm3 and undetectable viral load] are eligible.) - QTc Fridericia (QTcF) > 470 ms - History of myocardial infarction or unstable angina within 6 months prior to enrollment, troponin levels consistent with myocardial infarction, or clinically significant cardiac disease, such as ventricular arrhythmia requiring therapy, uncontrolled hypertension, or any history of symptomatic congestive heart failure - Acute or chronic uncontrolled pancreatitis or Child-Pugh Class C liver disease

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Zanidatamab
Administered intravenously (IV)
Evorpacept
Administered IV

Locations

Country Name City State
United States Pacific Center Medical Center, Inc. Anaheim California
United States University of Alabama at Birmingham Birmingham Alabama
United States University of Vermont Medical Center Burlington Vermont
United States University Hospitals Cleveland Medical Center Cleveland Ohio
United States Astera Cancer Care East Brunswick New Jersey
United States The University of Texas MD Anderson Cancer Center Houston Texas
United States Saint Luke's Cancer Institute Kansas City Missouri
United States UC San Diego - Moores Cancer Center La Jolla California
United States UCLA Department of Medicine Hematology/Oncology Los Angeles California
United States University of Wisconsin - Madison Madison Wisconsin
United States UC Irvine Health - Chao Family Comprehensive Cancer Center Orange California
United States Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania
United States Florida Cancer Specialists Sarasota Florida
United States Northwest Medical Specialties, PLLC Tacoma Washington

Sponsors (2)

Lead Sponsor Collaborator
Jazz Pharmaceuticals ALX Oncology Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of dose-limiting toxicities (DLTs; Part 1) Number of patients who experienced a DLT. DLTs include specifically defined adverse events (AEs) considered to be related to zanidatamab or evorpacept (ALX148), including combination of zanidatamab with evorpacept (ALX148) Up to 4 weeks
Primary Incidence of AEs (Part 1) Number of patients who experienced AEs, serious adverse events (SAEs), or adverse events of special interest (AESIs) Up to 7 months
Primary Incidence of clinical laboratory abnormalities (Part 1) Number of patients who experienced a Grade 3 or higher post-baseline laboratory abnormality, including either hematology or chemistry. Grades are defined using National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0 Up to 7 months
Primary Confirmed objective response rate (ORR)(Part 2) Number of patients who achieved a confirmed best overall response (BOR) of either complete response (CR) or partial response (PR) during treatment per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 Up to 2 years
Secondary Disease control rate (DCR)(Part 2) Number of patients who achieved a best response of CR, PR, or stable disease (SD) during treatment per RECIST 1.1 Up to 2 years
Secondary Clinical benefit rate (CBR)(Part 2) Number of patients who achieved a SD for = 24 weeks or a confirmed BOR of CR or PR during treatment per RECIST 1.1 Up to 2 years
Secondary Duration of response (DOR)(Part 2) The time from the first objective response (CR or PR) to documented progressive disease per RECIST 1.1, clinical progression, or death within 30 days of last dose of study drug (zanidatamab and/or evorpacept [ALX148]) from any cause Up to 2 years
Secondary Progression-free survival (PFS)(Part 2) The time from the first dose of study treatment to the date of documented disease progression (per RECIST 1.1), clinical progression, or death from any cause Up to 2 years
Secondary Progression-free survival 6 (PFS6)(Part 2) Number of patients with a PFS time = 24 weeks Up to 6 months
Secondary Overall survival (OS)(Part 2) The time from first dose of study treatment until death from any cause Up to 2 years
Secondary Incidence of AEs (Part 2) Number of patients who experienced AEs, SAEs, or AESIs Up to 7 months
Secondary Incidence of clinical laboratory abnormalities (Part 2) Number of patients who experienced a maximum severity of Grade 3 or higher post-baseline laboratory abnormality, including either hematology or chemistry. Grades are defined using NCI-CTCAE, version 5.0 Up to 7 months
Secondary Maximum serum concentration of zanidatamab and evorpacept (ALX148) (Part 2) Up to 7 months
Secondary Trough concentration of zanidatamab and evorpacept (ALX148) (Part 2) Minimum observed serum concentration (trough) Up to 7 months
Secondary Incidence of anti-drug antibodies (ADAs)(Part 2) Number of patients who develop ADAs Up to 7 months
See also
  Status Clinical Trial Phase
Active, not recruiting NCT02892123 - Trial of ZW25 (Zanidatamab) in Patients With Advanced HER2-expressing Cancers Phase 1
Active, not recruiting NCT03821233 - A Dose Finding Study of ZW49 in Patients With HER2-Positive Cancers Phase 1