Inclusion Criteria:
1. Male or female patients, 18 years of age or older at the time of consent.
2. Life expectancy of 6 months or greater as assessed by the treating oncologist.
3. Have advanced metastatic disease that has progressed on at least one line of
available therapy.
4. Histologically or cytologically confirmed diagnosis of Grade 3 well-differentiated
neuroendocrine tumor (NET) or poorly differentiated neuroendocrine carcinoma (NEC;
large-cell neuroendocrine carcinoma, small-cell carcinoma, mixed neuroendocrine non
neuroendocrine carcinoma). Note: if an archival tissue sample collected ≤ 2 years
from enrollment is unavailable at Screening for diagnostic confirmation, at the
Principal Investigator's (PI's) discretion, a screening biopsy will be ordered.
5. For patients in Part 1A, in addition to histological or cytological confirmation of
NEC or NET (see Inclusion #4), radiological confirmation of tumor is required.
6. Parts 1B and 2 only: Measurable disease as determined by Response Evaluation
Criteria in Solid Tumors (RECIST) v1.1 or immune-related Response Evaluation
Criteria in Solid Tumors (iRECIST). At least one lesion must be suitable for
multiple injections (up to 6 injections every 2 weeks) with SVV-001. Lesions for
injection must be ≥10 mm and ≤50 mm in longest diameter and deemed safe and suitable
for injection by the Investigator.
7. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
8. Recovered to Grade 1 or baseline from any clinically significant toxicity associated
with prior treatments (excluding alopecia) prior to initiation of investigational
medicinal product (IMP) administration.
9. Adequate hematological, renal, and liver function defined as follows:
Hepatic:
Serum alanine aminotransferase (ALT) and aspartate aminotransferase
(AST) ≤2.5 × upper limit of normal (ULN) (≤5 × ULN if liver metastases are
present)
Serum bilirubin ≤1.5 × ULN (unless due to Gilbert's syndrome or
hemolysis)
Renal:
Creatinine clearance ≥50 mL/minute using Cockcroft Gault equation.
Hematologic:
Absolute neutrophil count ≥1500 cells/µL.
Platelet count ≥100,000 platelets/µL.
Hemoglobin ≥9.0 g/dL.
International normalization ratio (INR) within the institutional
normal range.
Normal prothrombin time (PT) and partial thromboplastin time (PTT)
10. For Part 2 Expansion Cohort patients only, patients will submit archival tissue at
Screening and undergo a post-treatment biopsy according to the treating
institution's guidelines with the following exceptions:
If an archival tissue sample collected ≤ 2 years from enrollment is
unavailable at Screening, at the PI's discretion, a screening biopsy will be
ordered.
Participants will not undergo a biopsy procedure for collection of the
post-treatment biopsy if, in the discretion of their treating physician, the
participant's condition has deteriorated to the point where performance of a
biopsy procedure would place the participant at an increased risk for
complications beyond what is reasonably expected for a biopsy collected as part
of the participant's standard medical care.
11. Women of childbearing potential must agree to use a reliable form of contraceptive
during the trial treatment period and for at least 7 months following the last dose
of IMP.
12. Male patients must agree to use an adequate method of contraception during the trial
treatment period and for at least 7 months following the last dose of IMP.
13. Patient is willing and able to comply with all protocol-required assessments,
visits, and procedures.
14. Provide written informed consent prior to performing any trial-related procedure.
Exclusion Criteria:
1. Any active second malignancy within the 2 years prior to the screening visit, unless
the patient has undergone curative surgery for the tumors such as in situ cervical
cancer or squamous cell cancer of the skin.
2. Has had cytotoxic chemotherapy or radiation therapy within 3 weeks; and less than 5
half-lives or 6 weeks, whichever is shorter, from prior biologic therapies, prior to
the first dose of SVV-001.
3. Has undergone a major surgical procedure (as defined by the Investigator) or
significant traumatic injury within 28 days prior to the first dose of SVV-001.
4. Has any physical abnormality of the tissue/organ to be biopsied that would put the
patient at increased risk of bleeding secondary to the injection and/or biopsy.
5. Has received a live-virus immunization within 30 days prior to the screening visit
or anticipates receiving a live virus immunization during the trial or within 30
days of the last treatment with IMP.
6. Presence of an active autoimmune or inflammatory disease requiring systemic
treatment within the past 2 months or a documented history of clinically severe
autoimmune disease that requires systemic steroids or other immunosuppressive
medications. Local steroid injections, intermittent use of topical, inhaled,
ophthalmologic, intra-articular, or intranasal corticosteroids, or systemic
corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or
equivalent would not result in exclusion from the trial.
7. Presence of primary immunodeficiency or receiving systemic steroids of >10 mg/day
prednisone or equivalent or other immunosuppressive agents within 14 days prior to
the first dose of SVV-001.
8. Any active infection, including known infection with human immunodeficiency virus
(HIV), active hepatitis, or seropositive for hepatis B immunoglobulin (Ig) M core
antibody or hepatitis C ribonucleic acid (RNA) at the screening visit.
9. Patients with a history of solid-organ or bone marrow transplant.
10. Known hypersensitivity to ipilimumab or nivolumab or their excipients. 11. Has known untreated central nervous system metastases. Patients with treated brain
metastases are eligible as long as they are stable and there is no evidence of
progression for at least 4 weeks after central nervous system-directed treatment, as
ascertained by clinical examination and brain imaging (magnetic resonance imaging
(MRI) or computed tomography (CT)) during the screening period.
12. Any clinically significant (i.e., active) cardiovascular disease, including cerebral
vascular accident/stroke (<6 months prior to enrollment), myocardial infarction (<6
months prior to enrollment), unstable angina, congestive heart failure (≥ New York
Heart Association Classification Class II), or serious cardiac arrhythmia requiring
medication.
13. Patients with an ejection fraction (EF) < 50 on a 2D echocardiogram (ECHO).
14. Patients whose baseline pulse oximetry (saturation of peripheral oxygen (SpO2)) is <
92% on Room air.
15. Any chronic illness, psychiatric condition, or social situation that is life
threatening or, in the opinion of the Investigator, renders the patient unsuitable
for participation in a clinical trial due to possible noncompliance or would place
the patient at an unacceptable risk and/or have the potential to affect
interpretation of the results of the trial.
16. Female participants who are breastfeeding and/or who have a positive pregnancy test
result prior to receiving any treatment with IMP.
17. Patients with impaired decision-making capacity.
