A Phase 1 Open Label, Multicenter, Multiple Ascending Dose Trial Evaluating the Safety, Tolerability and Immunogenicity of Intramuscular Recombinant NY-ESO-1 Protein With GLA-SE Adjuvant in Patients With Unresectable or Metastatic Cancer
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Melanoma
- Sponsor
- Immune Design, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
- Enrollment
- 13
- Locations
- 4
- Primary Endpoint
- Safety and tolerability
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This is a Phase I, multi-center, multiple ascending dose study to evaluate the clinical safety and immune response of IDC-G305 when injected intramuscularly in patients with unresectable or metastatic cancer. IDC-G305 is an immunotherapy consisting of recombinant NY-ESO-1 antigen and the adjuvant, GLA-SE. The goal is for IDC-G305 to stimulate the body's immune system to fight the spread and growth of cancer for patients whose tumors include the NY-ESO-1 protein. Patients with melanoma, ovarian, renal cell or non-small cell lung cancer may be considered for the trial.
Detailed Description
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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Safety and tolerability
Time Frame: Up to 1 year after last vaccination
To evaluate the safety and tolerability of multiple ascending doses of intramuscular (IM) IDC-G305
Secondary Outcomes
- Immunogenicity(Approximately 12 weeks)