| Eligibility |
Inclusion Criteria:
Phase 1a
1. Patients must have histologically or cytologically documented metastatic or advanced
epithelial cancer that has relapsed from or is refractory to standard treatment, or
for which no standard treatment is available.
2. At least one measurable site of disease according to RECIST v1.1 criteria; this lesion
must be either (i) outside a previously irradiated area or (ii) progressive if it is
in a previously irradiated area
3. Tumour accessible for biopsy, biopsy deemed safe by the Investigator, and patient
willing to consent to tumour biopsies
4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
All patients
1. Provide written informed consent to participate
2. Aged 18 years or over on day of signing informed consent
3. Predicted life expectancy of =6 months
4. Adequate lung reserve
5. Adequate renal function
6. Adequate hepatic function
7. Adequate bone marrow/haematological function
8. Meeting reproductive status requirements
Exclusion criteria
1. Prior or planned allogeneic or autologous bone marrow or tissue/organ transplantation
2. Splenectomy
3. Active infections requiring systemic anti-infective treatment, physician
monitoring/hospital admission or recurrent fevers (>38.0°C) associated with a clinical
diagnosis of active infection
4. Treatment with the antiviral agents: ribavirin, adefovir, lamivudine, cidofovir or
paxlovid within 10 days prior to the first dose of study treatment; or pegylated
interferon in the 4 weeks before the first dose of study treatment
5. Known history of hepatitis B infection or known active hepatitis C infection. Known
history of HIV infection
6. 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 chronic systemic immunosuppressive treatment
7. Treatment with any live, live-attenuated or COVID-19 vaccine in the 30 days before
first dose of study drug
8. Treatment with any other vaccine (including known non live/live-attenuated or
non-adenoviral COVID-19 vaccines) in the 7 days before first dose of study drug
9. History of prior Grade 3-4 acute kidney injury or other clinically significant renal
impairment
10. History of clinically significant interstitial lung disease or non-infectious
pneumonitis/interstitial lung disease that required steroids (or current
pneumonitis/interstitial lung disease)
11. Lymphangitic carcinomatosis
12. Infectious or inflammatory bowel disease in the 3 months before the first dose of
study treatment
13. Any known CTCAE Grade =2 coagulation abnormality/coagulopathy
14. Any clinically significant cardiovascular, peripheral vascular, cerebrovascular, or
thromboembolic event in the 6 months before the first dose of study treatment
15. Grade 3 or 4 gastrointestinal bleeding (or risk factors for gastrointestinal
bleeding), haemoptysis, or any history of bleeding requiring an investigative
procedure, transfusion or hospitalization in the 6 months before the first dose of
study treatment
16. Tumour location/extent considered by the Investigator to present a significant risk if
tumour flare or necrosis were to occur
17. Use of the following prior therapies/treatments :
- Treatment with any other enadenotucirev-based virus (parent virus or
transgene-modified variants), or anti-CD40 antibody at any time
- Radiation therapy to the lung that is >30Gy within 6 months of the first dose of
trial treatment
- Treatment with an investigational or licensed anti-cancer monoclonal antibody
(mAb), immune checkpoint inhibitor, immune stimulatory treatment or other
biological therapy in the 28 days prior to the first dose of study treatment.
- Prior anti-PD-1 / PD-L1 therapy is permitted without a 'washout' phase
- Treatment with an investigational or licensed chemotherapy, targeted small
molecule or other investigational drug in the 14 days or five half-lives
(whichever is shorter) before the first dose of study treatment
- Major surgery in the 28 days before the first dose of study treatment or
radiation therapy in the 14 days before the first dose of study treatment
- Bisphosphonate therapy or treatment with Receptor Activator of Nuclear factor
Kappa-? (RANK)-ligand inhibitors for metastatic bone disease is permitted
18. All toxicities attributed to prior anti-cancer therapy must have resolved to Grade 1
or baseline before the first dose of study treatment. (see protocol for exceptions)
19. Participants with a history of radiation pneumonitis are not eligible for inclusion
20. Discontinuation from prior treatment with an anti-PD-1 or anti PD L1/PD-L2 agent, or
an agent directed to another stimulatory or co-inhibitory T cell receptor, due to a
Grade =3 immune-related AE
21. Known allergy or hypersensitivity (Grade =3) to NG-350A transgene, pembrolizumab
and/or any of its excipients or other monoclonal antibodies
22. Known hypersensitivity to both cidofovir and valacyclovir
23. Other prior malignancy active within the previous 3 years (see protocol for
exceptions)
24. Known active central nervous system metastases and/or carcinomatous meningitis.
Participants with previously treated brain metastases may participate provided they
are radiologically stable, i.e. without evidence of progression for at least 4 weeks
by repeat imaging (note that the repeat imaging should be performed during study
screening), clinically stable and have not required steroid treatment for at least 14
days prior to first dose of study treatment
25. Positive pregnancy test prior to treatment (a serum test must be performed within 24
hours)
26. History or current evidence of any condition, therapy, or laboratory abnormality, or
other circumstance that might confound the results of the study or interfere with the
participant's participation for the full duration of the study, such that it is not in
the best interest of the participant to participate, in the opinion of the treating
investigator
27. Known psychiatric or substance abuse disorder that would interfere with the
participant's ability to cooperate with the requirements of the study
|
