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Trial record 1 of 1 for:    CF33-hNIS-antiPDL1
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CF33-hNIS-antiPDL1 for the Treatment of Metastatic Triple Negative Breast Cancer

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ClinicalTrials.gov Identifier: NCT05081492
Recruitment Status : Recruiting
First Posted : October 18, 2021
Last Update Posted : March 18, 2022
Sponsor:
Collaborators:
National Cancer Institute (NCI)
Imugene Limited
Information provided by (Responsible Party):
City of Hope Medical Center

Brief Summary:
This phase I trial tests the safety, side effects, and best dose of CF33-hNIS-antiPDL1 in treating patients with triple negative breast cancer that has spread to other places in the body (metastatic). CF33-hNIS-antiPDL1 is an oncolytic virus. This is a virus that is designed to infect tumor cells and break them down.

Condition or disease Intervention/treatment Phase
Anatomic Stage IV Breast Cancer AJCC v8 Metastatic Triple-Negative Breast Carcinoma Prognostic Stage IV Breast Cancer AJCC v8 Biological: Oncolytic Virus CF33-expressing hNIS/Anti-PD-L1 Antibody Phase 1

Detailed Description:

PRIMARY OBJECTIVE:

I. To determine the safety and tolerability of a novel chimeric oncolytic orthopoxvirus, oncolytic virus CF33-expressing hNIS/Anti-PD-L1 antibody (CF33-hNIS-antiPDL1), by the evaluation of toxicities including: type, frequency, severity, attribution, time course, reversibility and duration according to Common Terminology Criteria for Adverse Events (CTCAE) 5.0 criteria.

SECONDARY OBJECTIVES:

I. To determine the optimal biologic dose (OBD) (defined as a safe dose that induces an immune response in tumors [increase checkpoint target PD-L1 by at least 5% and/or increase T cell infiltration by at least 10%]) and the recommended phase II dose (RP2D) for future expansion trial.

II. To determine tumor response rates by Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1 (primary) and immune-modified (i)RECIST (secondary).

III. To document possible therapeutic efficacy and evaluate progression-free survival, overall survival and response.

EXPLORATORY OBJECTIVE:

I. To determine the immune and genomic profiles of tumors before and after CF33-hNIS-antiPDL1 therapy.

OUTLINE: This is a dose-escalation study.

Patients receive CF33-hNIS-antiPDL1 intratumorally (IT) on days 1 and 15. Treatment repeats every 28 days for up to 3 cycles in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days, then every 3 months for 1 year.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 78 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase I, First-in-Human Study of Intratumoral Administration of CF33-hNIS-antiPDL1, A Novel Chimeric Oncolytic Poxvirus Encoding Human Sodium Iodide Symporter (HNIS) in Patients With Metastatic Triple Negative Breast Cancer
Actual Study Start Date : October 18, 2021
Estimated Primary Completion Date : October 1, 2023
Estimated Study Completion Date : October 1, 2023

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
Experimental: Treatment (CF33-hNIS-antiPDL1)
Patients receive CF33-hNIS-antiPDL1 IT on days 1 and 15. Treatment repeats every 28 days for up to 3 cycles in the absence of disease progression or unacceptable toxicity.
Biological: Oncolytic Virus CF33-expressing hNIS/Anti-PD-L1 Antibody
Given IT
Other Names:
  • CF33 Expressing hNIS-Anti-PD-L1 Antibody
  • CF33-hNIS-antiPDL1




Primary Outcome Measures :
  1. Incidence of adverse events [ Time Frame: Up to 30 days ]
    Toxicity will be graded according to the National Cancer Institute-Common Terminology Criteria for Adverse Events version 5.0. Observed toxicities/adverse events will be summarized in terms of type (organ affected or laboratory determination), severity, time of onset, duration, probable association with the study treatment and reversibility or outcome.


Secondary Outcome Measures :
  1. Immune Biomarker Expression [ Time Frame: Up to 6 months ]

    Changes (%) in PD1 expression compared to baseline by immunohistochemistry

    Changes (%) in PD-L1 expression compared to baseline by immunohistochemistry

    Changes (%) CTLA-4 expression compared to baseline by immunohistochemistry

    Changes (%) CD8 cell quantification compared to baseline by Immunohistochemistry


  2. Optimal biologic dose [ Time Frame: Up to 3 months ]
    Defined as safe dose that induces an immune response in tumors (increase checkpoint target PD-L1 by at least 5% and/or increase T cell infiltration by at least 10%).

  3. Response rate based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 [ Time Frame: Up to 6 months ]
    Will estimate the response rate by the percent of evaluable patients and its 95% confidence interval (C.I.) by the exact method.

  4. Response rate based on immune related iRECIST [ Time Frame: Up to 6 months ]
    Will estimate the response rate by the percent of evaluable patients and its 95% C.I. by the exact method.

  5. Progression free survival [ Time Frame: Up to 1 year ]
    Will be estimated using the Kaplan-Meier product-limit method.

  6. Clinical benefit rate [ Time Frame: Up to 6 months ]
    Percentage of patients who achieved Partial Response/ Complete Response/ Stable disease at 6 months

  7. Event-free survival [ Time Frame: Up to 3 years ]
    Event-free survival (EFS): defined as the duration of time from start of protocol treatment to time of disease relapse/progression or death due to any cause, whichever occurs earlier.

  8. Duration of response [ Time Frame: Up to 3 years ]
    Duration of response (DOR): defined as the time from the first achievement of PR and CR to time of PD.

  9. Overall survival [ Time Frame: Up to 3 years ]
    Will be estimated using the Kaplan-Meier product-limit method.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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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:

  • Documented informed consent of the participant and/or legally authorized representative

    • Assent, when appropriate, will be obtained per institutional guidelines
  • Agreement to research biopsies on study, once during study and end of study, exceptions may be granted with study principal investigator (PI) approval
  • >= 18 years
  • Eastern Cooperative Oncology Group (ECOG) =< 2
  • Histologically confirmed metastatic triple negative breast cancer. Triple negative status will be defined as estrogen receptor (ER) and progesterone receptor (PR) =< 10% by immunohistochemistry (IHC) and HER2 negative, per American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) guidelines
  • Measurable disease by RECIST 1.1
  • Patients must have progressed on or been intolerant of at least 2 prior lines of therapy for advanced/metastatic disease. Patients that qualify for immunotherapy and/or PARP inhibitors must have progressed on or been intolerant of these agents
  • Fully recovered from the acute toxic effects (except alopecia) to =< grade 2 to prior anti-cancer therapy
  • Must have a superficial tumor (cutaneous, subcutaneous), breast lesion or nodal metastases amenable to safe repeated intratumoral injections per treating physician and interventional radiologist review
  • Absolute neutrophil count (ANC) >= 1,500/mm^3

    • NOTE: Growth factor is not permitted within 14 days of ANC assessment unless cytopenia is secondary to disease involvement
  • Platelets >= 100,000/mm^3

    • NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
  • Total bilirubin =< 1.5 X upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) =< 2.5 x ULN

    • If liver metastases are present: AST =< 5 x ULN
  • Alanine aminotransferase (ALT) =< 2.5 x ULN

    • If liver metastases are present: ALT =< 5 x ULN
  • Serum creatinine =< 1.5 mg/dL or creatinine clearance of >= 50 mL/min per 24 hour urine test or the Cockcroft-Gault formula
  • Prothrombin (PT) =< 1.5 x ULN
  • Activated partial thromboplastin time (aPTT) =< 1.5 x ULN
  • Women of childbearing potential (WOCBP): negative serum pregnancy test
  • Agreement by females and males of childbearing potential* and their partners to use an effective method of birth control (defined as a hormonal or barrier method) or abstain from heterosexual activity for the course of the study through at least 6 months after the last dose of protocol therapy

    • Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only)

Exclusion Criteria:

  • Chemotherapy, biological therapy, immunotherapy or investigational therapy within 14 days prior to day 1 of protocol therapy
  • Major surgery or radiation therapy within 28 days of study therapy
  • Has received a vaccination within 30 days of first study injection
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent
  • Clinically significant uncontrolled illness
  • Active infection requiring antibiotics
  • Known history of immunodeficiency virus (HIV)
  • Patients with a known history of hepatitis B or hepatitis C infection who have active disease as evidenced by hepatitis (Hep) B surface antigen status or Hep C polymerase chain reaction (PCR) status obtained within 14 days of cycle 1, day 1
  • Another malignancy within 3 years, except non-melanomatous skin cancer
  • Females only: Pregnant or breastfeeding
  • Patients may not have clinically unstable brain metastases. Patients may be enrolled with a history of treated brain metastases that are clinically stable for >= 4 weeks prior to start of study treatment
  • Any other condition that would, in the Investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
  • Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

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): NCT05081492


Locations
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United States, California
City of Hope Medical Center Recruiting
Duarte, California, United States, 91010
Contact: Yuan Yuan    626-256-4673    Yuyuan@coh.org   
Principal Investigator: Yuan Yuan         
Sponsors and Collaborators
City of Hope Medical Center
National Cancer Institute (NCI)
Imugene Limited
Investigators
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Principal Investigator: Yuan Yuan City of Hope Medical Center
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Responsible Party: City of Hope Medical Center
ClinicalTrials.gov Identifier: NCT05081492    
Other Study ID Numbers: 21094
NCI-2021-08983 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
21094 ( Other Identifier: City of Hope Medical Center )
P30CA033572 ( U.S. NIH Grant/Contract )
First Posted: October 18, 2021    Key Record Dates
Last Update Posted: March 18, 2022
Last Verified: March 2022

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Additional relevant MeSH terms:
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Breast Neoplasms
Triple Negative Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Antibodies
Immunoglobulins
Immunologic Factors
Physiological Effects of Drugs