Study of HF10 in Patients With Refractory Head and Neck Cancer or Solid Tumors With Cutaneous and/or Superficial Lesions

Completed · Phase 1

Conditions studied: Refractory Head and Neck Cancer, Squamous Cell Carcinoma, Skin, Carcinoma of the Breast, Malignant Melanoma

In brief

The purpose of this study is to determine whether HF10 is safe and effective in the treatment of head and neck cancer or solid tumors with cutaneous and/or superficial lesions.

Key facts

Study ID

NCT01017185

Run by

Takara Bio Inc.

People needed

28

Starts

2009-08-01

Expected to finish

2015-03-01

Last updated by the study team

2019-05-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must have histologically confirmed solid tumors that have failed standard therapies (surgery, chemotherapy, radiotherapy, or endocrine therapy) and for which no curative options exist, including, but not limited to:
• Squamous cell carcinoma of the head and neck
• Squamous cell carcinoma of the skin
• Carcinoma of the breast
• Malignant melanoma
• Patients may have had any kind and number of prior cancer therapies.
• Patients must have measurable non-visceral lesions that are evaluable by the RECIST method
• The tumor mass to be treated must be non-visceral and adequate for injection (i.e., more than 2 cm away from major vascular structures) and measurement by RECIST.
• Patients in Stage 1 must be seropositive for HSV-1.
• The first patient enrolled into each cohort in Stage 2 must be seropositive for HSV-1.
• Patients must be ≥ 18 years of age.
• Patients must have a life expectancy ≥ 12 weeks
• Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
• Patients must have adequate hepatic function, as defined as
• Total bilirubin levels ≤ 1.5 x upper limit of normal (ULN)
• AST/ALT levels ≤ 2.5 x ULN, or ≤ 5 x ULN if liver metastases are present
• Patients must have adequate renal function as defined as serum creatinine ≤ 1.5 x ULN or creatinine clearance (calculated) ≥ 60 mL/min/1.73 m2 for patients with creatinine > 1.5 x ULN
• Patients must have adequate bone marrow function, as defined as
• Absolute neutrophil count ≥ 1,500/μL and
• Platelet count ≥ 100,000/μL
• Patients must have no known bleeding diathesis or coagulopathy that would make intratumoral injection or biopsy unsafe.
• Men and women of childbearing potential must agree to use adequate contraception prior to study entry and for up to six months.
• Females of childbearing potential must have a negative urine or serum pregnancy test within one week prior to start of treatment.
• Patients must be able to understand and willing to sign a written informed consent document.

You may not qualify if…

• Patients receiving chemotherapy or radiotherapy within 4 weeks of injection of HF10, or adverse events > Grade 1, except alopecia, resulting from agents administered more than 4 weeks prior to HF10 injection.
• Patients with a history of significant tumor bleeding, or coagulation or bleeding disorders.
• Patients with nasopharyngeal tumors.
• Patients with deep (below the platysma muscle layer) ulcerative tumors.
• Patients with target tumors that could potentially invade a major vascular structure(s) (e.g., innominate artery, carotid artery), based on unequivocal imaging findings, as determined by a radiologist.
• Patients with Grade ≥ 1 pre-existing neurologic abnormalities (CTCAE version 3.0).
• Patients who have been hospitalized for emergent conditions requiring inpatient evaluation, treatment or procedure during the 30 days prior to entry on study. In addition, emergent conditions requiring inpatient evaluation, treatment or procedure must have resolved or be medically stable and not severe for 30 days prior to entry on study.
• Patients with clinically evident Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), Hepatitis C virus (HCV), or Epstein-Barr virus (EBV) infection. Patients will be tested for HIV during pre-treatment screening.
• Patients receiving steroids or immunosuppressive agents, e.g., for rheumatoid arthritis
• Concurrent use of any other investigational agents.
• Presence or history of central nervous system metastasis.
• Pregnant or breastfeeding women;women desiring to become pregnant within the timeframe of the study are also excluded.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

Where it is running

• Montefiore Medical Center — The Bronx, New York, United States
• Oregon Health and Science University — Portland, Oregon, United States
• University of Pittsburgh — Pittsburgh, Pennsylvania, United States
• Mary Crowley Cancer Research Center — Dallas, Texas, United States
• Huntsman Cancer Institute — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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