| Eligibility |
Inclusion Criteria:
1. Newly diagnosed or recurrence of clinical stage III-IVb, histologically confirmed oral
cavity, larynx, hypopharynx or oropharynx SCCHN (T1 with N2-3; T2 with N2-3; T3 with
N0-3; T4a with N0-3)
2. Disease is considered resectable, definitive surgery is planned in the next 8 weeks
from screening, and the patient is willing to undergo surgery (potential for 2-3 cm of
resected tumour specimen to be available for translational research purposes)
3. Provide written informed consent to participate
4. Aged 18 years or over
5. Willing to consent to tumour biopsies at baseline
6. ECOG performance status 0 or 1
7. Ability to comply with study procedures in the Investigator's opinion
8. Adequate renal function
9. Adequate hepatic function
10. Adequate bone marrow function
11. Meeting reproductive status requirements
Exclusion Criteria:
1. Prior allogeneic or autologous bone marrow or organ transplantation
2. Active infections requiring antibiotics, physician monitoring or recurrent fevers
(>38.0°C) associated with a clinical diagnosis of active infection. Active infection
requiring systemic therapy within 1 week of the anticipated first dose of study drug
3. Active viral disease or positive test for hepatitis B virus, hepatitis C virus (HCV)
or HIV/AIDS
4. Patients who have active autoimmune disease that has required systemic therapy in the
past 2 years, are immunocompromised in the opinion of the Investigator, or are
receiving systemic immunosuppressive treatment (see protocol for full criteria)
5. Treatment with any COVID-19 vaccine in the 28 days before the first dose of NG-641,
unless the vaccine is known to not be based on an adenoviral vector (e.g., mRNA
vaccines)
6. Treatment with any vaccine (including known non-adenoviral COVID-19 vaccines) in the 7
days before first dose of NG-641
7. History of clinically significant chronic liver disease
8. History of clinically significant interstitial lung disease (including pneumonitis)
9. History of prior Grade 3-4 acute kidney injury or other clinically significant renal
impairment
10. Use of antiviral agents
11. Incomplete recovery from surgery, incomplete healing of an incision site or evidence
of infection
12. Any of the following in the 3 months before the first dose of study treatment: Grade 3
or 4 gastrointestinal bleeding or risk factors for gastrointestinal bleeding,
infectious or inflammatory bowel disease, pulmonary embolism or other uncontrolled
thromboembolic event, history or evidence of haemoptysis, or significant
cardiovascular or cerebrovascular event
13. Any known Common Terminology Criteria for Adverse Events (CTCAE) Grade =2 coagulation
abnormality/coagulopathy
14. Prior history of bowel obstruction, or infectious or inflammatory bowel disease in the
3 months before the first dose of study treatment
15. Major surgery or treatment with any chemotherapy, radiation therapy, biologics for
cancer or investigational drug/therapy in the 28 days before the first dose of study
treatment:
• All toxicities attributed to prior anti-cancer therapy other than alopecia must have
resolved to Grade 1 or baseline before the first dose of study treatment. Patients
with toxicities (other than renal toxicities) attributed to prior anti-cancer therapy
which are not expected to resolve and result in long lasting sequelae, such as
neuropathy after platinum-based therapy, are permitted to enrol
16. Other prior malignancy active within the previous 3 years
17. Tumour location/extent considered by the Investigator to present a significant risk of
airway obstruction if tumour flare or necrosis were to occur
18. Any serious or uncontrolled medical disorder that, in the opinion of the Investigator
or the Medical Monitor, may increase the risk associated with study participation or
study treatment administration, impair the ability of the patient to receive protocol
therapy or interfere with the interpretation of study results
19. Previous treatment with any other enadenotucirev-based therapy, or fibroblast
activation protein (FAP) targeting agent
20. Known allergy/immune-related adverse reactions to NG-641 transgene or immune
checkpoint inhibitor products or formulation; severe hypersensitivity to another
monoclonal antibody
21. Any other medical or psychological condition that would affect the patient's ability
to comply with all visits and assessments, or compromise ability to give informed
consent
22. Related to or a dependent of the site staff, or a member of the site staff.
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