A Phase 1 Trial of NY-ESO-1 With GLA-SE in Patients With Unresectable or Metastatic Cancer

This is a Phase 1, open label, multicenter, multiple ascending dose trial of IDC-G305
administered by intramuscular injection in a 3+3 sequential dose escalation design.
IDC-G305 is an immunotherapy consisting of recombinant NY-ESO-1 antigen and the adjuvant,
GLA-SE. Patients with unresectable, relapsed or metastatic cancer but with low disease
burden and indolent disease course may be considered for the trial. Tumors must express the
NY-ESO-1 gene signature and tumor types that will be studied are: melanoma, ovarian,
sarcoma,non-small cell lung and breast cancer.

Each of three dose level cohorts will be treated contingent upon absence of dose limiting
toxicity (DLT) and acceptable safety data for the preceding cohort. Initially, three
patients will be scheduled to receive IDC-G305 in each dose level cohort. Dose escalation
will be contingent upon the assessment of safety data obtained during the initial
injections.

Patients will be evaluated at baseline and at regular intervals for safety and immune
response. Both cellular and humoral immunogenicity will be explored.

Inclusion Criteria:

- Confirmed diagnosis of melanoma, ovarian cancer, sarcoma, breast cancer or non-small
cell lung cancer (NSCLC)

- Unresectable, relapsed and/or metastatic cancer with minimal or low disease burden.
Disease may or may not be measurable and should not be rapidly progressive.
Inadequate response, relapse and/or unacceptable toxicity with one or more prior
systemic, surgical, or radiation cancer therapies, except patients with NSCLC and
breast cancer who must have experienced an inadequate response and/or unacceptable
toxicity with two or more prior systemic, surgical, or radiation cancer therapies.

- Cancer expresses NY-ESO-1

- ≥ 18 years of age

- Life expectancy of ≥ 6 months

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

- ECG without evidence of clinically significant arrhythmia or ischemia

- Negative pregnancy test for females of childbearing potential

Exclusion Criteria:

- Pregnant or nursing

- Vaccine or other therapy directed against NY-ESO-1 at any time in the past and any
investigational therapy within three weeks prior to IDC-G305 dosing

- Significant immunosuppression

- Cancer chemotherapy, G-CSF or GM-CSF within three weeks prior to the first study
treatment

- Significant autoimmune disease

- Myocardial infarction within six months of treatment, active cardiac ischemia or
Grade III or IV heart failure

- Inadequate hematology or chemistry profiles

- History of other cancer within three years

- Active, concurrent or recent infection, including tuberculosis, hepatitis B,
hepatitis C or HIV

- Uveal melanoma

- Brain metastases considered unstable