Status:

ACTIVE_NOT_RECRUITING

Assessing the Immunogenicity of pING-hHER3FL

Lead Sponsor:

Herbert Lyerly

Conditions:

Advanced Cancer

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

This study is a phase I clinical trial will that will use an investigational cancer vaccine called pING-hHER3FL. pING-hHER3FL is a circular piece of DNA that produces the full length human HER3 protei...

Detailed Description

The human epidermal growth factor receptor (HER) family including HER1 (also known as EGFR), HER2, HER3 and HER4 (also known as ErbB2, ErbB3, and ErbB4 respectively) is an important receptor family fo...

Eligibility Criteria

Inclusion

  • Documented history of solid tumor where HER3 expression is expected (this includes breast, colon, lung, prostate, ovarian, cervical, endometrial, gastric, pancreatic, bladder, head and neck, liver, and esophageal cancer, but other tumors will be considered based on emerging HER3 expression data in the literature). Demonstration of HER3 expression is not required for enrollment.
  • Has undergone surgical resection of malignancy and has completed intended standard course of chemotherapy and HER2 targeted therapy and radiotherapy under the direction of their physician. Subjects may continue on adjuvant hormonal therapy.
  • Has no evidence of disease by standard imaging studies (performed at the direction of their physician) within 60 days prior to initiating study treatment.
  • Between 3 weeks and 2 years since prior cytotoxic chemotherapy, HER2-targeted therapy or radiotherapy to the start of study treatment.
  • ECOG 0 or 1
  • Estimated life expectancy \> 3 months.
  • Age ≥ 18 years.
  • Adequate hematologic function, with ANC \>1500/µL, Hemoglobin ≥ 9 g/dL, and Platelets ≥ 75,000/µL.
  • Adequate renal and hepatic function, with Serum Creatinine \< 1.5 mg/dL, Bilirubin \< 1.5 mg/dL (except for Gilbert's syndrome which will allow bilirubin ≤ 2.0 mg/dL), ALT and AST ≤ 2.5 x ULN or if liver metastases are present \< 5 x ULN.
  • Female patients must be of non-child-bearing potential or use effective contraception, .
  • Labs performed as standard of care prior to signing consent can be used to fulfill eligibility requirements if they were performed within 4 weeks of the start of study treatment.
  • Ability to understand and provide signed informed consent.
  • Ability to return to the study site for adequate follow-up, as required by this protocol.
  • Negative serum pregnancy test within 7 days prior to the start of study treatment, for women of childbearing potential only.

Exclusion

  • Patients must have recovered to Grade 1 toxicities from any prior treatment(s).
  • Known CNS/brain metastases
  • History of auto-immune disease such as, but not restricted to, inflammatory bowel disease, systemic lupus erythematosus, ankylosing spondylitis, scleroderma, or multiple sclerosis.
  • Serious chronic or acute illness considered by the Principal Investigator to constitute an unwarranted high risk for investigational treatment.
  • Medical or psychological impediment to probable compliance with the protocol.
  • Concurrent or prior second malignancy (within the past 5 years) other than non-melanoma skin cancer, Carcinoma in situ of the bladder and cervix.
  • Presence of active infection or systemic use of antimicrobials within 48 hours prior to the start of study treatment.
  • Patients on continuous steroid therapy for at least 72 hours (or other continuous immunosuppressives such as azathioprine or cyclosporine A) are excluded on the basis of potential immune suppression.
  • Presence of a known active acute or chronic infection including HIV or viral hepatitis (Hepatitis B and C).
  • Pregnant or nursing women.
  • Prior immunotherapy

Key Trial Info

Start Date :

July 13 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2030

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT03832855

Start Date

July 13 2020

End Date

March 1 2030

Last Update

July 3 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Duke University Medical Center

Durham, North Carolina, United States, 27710

Assessing the Immunogenicity of pING-hHER3FL | DecenTrialz