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Clinical Evaluation of the New Hypoxia Imaging Agent HX4

Clinical Evaluation of the New Hypoxia Imaging Agent HX4

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01213030
Enrollment
12
Registered
2010-10-01
Start date
2009-06-30
Completion date
2010-05-31
Last updated
2012-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Cancer, Liver Cancer, Lung Cancer

Keywords

HX4, [F-18]HX4, FMISO, [F-18]FMISO, Solitary Tumor, Hypoxia

Brief summary

Positron Emission Tomography (PET) with fluorine-18 fluoromisonidazole (FMISO) has been used for several years as a non invasive imaging technique to study tumor hypoxia. Several experimental and clinical studies have indicated that FMISO uptake of tissues is correlated with tissue oxygen tension and that FMSO PET allows non-invasive differentiation between hypoxic and normoxic tumors. Currently, FMISO-PET represents the best characterized and validated noninvasive hypoxia imaging technique. Nevertheless, clinical studies have also shown the limitations of FMISO PET. Accumulation of FMISO in hypoxic tumors is relatively low, resulting in a low contrast between hypoxic tumors and surrounding normal tissues. In addition, imaging needs to be started relatively late after tracer injection (about 3 hours post-injection), when a significant percentage of the fluorine-18 label has already decayed and the count statistics of the PET images are relatively low. Because of these limitations, FMISO PET is still only used at a few research centers, despite high clinical interest in hypoxia imaging.

Detailed description

Objective of the study The aim of this study is to: * evaluate a hypoxia imaging agent, HX4, in patients with solitary tumors (i.e., locally advanced head and neck cancer) * gain information on bio-distribution of \[F-18\]HX4 * compare the PET images of \[F-18\] FMISO to \[F-18\]HX4 for resolution, signal to background ratio, and tumor/blood ratio

Interventions

DRUG[F-18] FMISO

10 mCi \[F18\] HX4 and 10 mCi \[F-18\] FMISO within 7 days of each other regardless of sequence

10 mCi \[F18\] HX4 and 10 mCi \[F-18\] FMISO within 7 days of each other regardless of sequence

Sponsors

Fudan University
CollaboratorOTHER
Siemens Molecular Imaging
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient may be male or female and of any race / ethnicity * Patient is \> 18 years old at the time of investigational product administration * Patient or patient's legally acceptable representative provides written informed consent * Patient is capable of complying with study procedures * Patient is capable of communicating with study personnel * Patient must have histologically confirmed stage III, or IV squamous cell carcinoma of the head and neck whose primary origin was from the oral cavity, oropharynx, hypopharynx, or larynx. * According to the Karnofsky Performance Status Scale, the patient has a value of ≥ 60% at time of screening * Patient must have normal organ and renal function as defined: * total bilirubin within normal institutional limits * AST(SGOT)/ALT(SGPT) less than or equal to 2.5 x institutional upper limits of normal * creatinine within normal institutional limits * BUN within normal institutional limits * PT and PTT \< 2.0 x institutional upper limits of normal

Exclusion criteria

* Patient is younger than 18 years old at the time of investigational product administration * Female patient is pregnant or has a positive serum pregnancy test * Patient is unable to remain still for duration of imaging procedure * Patient has a history of significant renal disease * Patient has previously received \[F-18\]HX4 at any time, or any other investigational product in the past thirty days. * Patient has been involved in an investigative, radioactive research procedure within the past year * Inadequate tumor sites or volume to allow for biopsy * Patient has any other condition or personal circumstance that, in the judgment of the investigator, might interfere with the collection of complete and good quality data

Design outcomes

Primary

MeasureTime frame
Efficacy of a hypoxia imaging agent, HX4, in patients with solitary tumors (i.e., locally advanced head and neck cancer)6 months

Secondary

MeasureTime frame
Resolution, signal to background ratio, and tumor/blood ratio of PET images with [F-18] FMISO and [F-18]HX46 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026