Modified Vaccine for High Risk or Low Residual Melanoma Patients
Recruiting now · Phase 1/Phase 2
Conditions studied: Malignant Melanoma
In brief
This study is designed for patients who had malignant melanoma and, following tumor removal, are now free of disease, or have only very minor residual disease, and are at a very high risk of disease recurrence. These patients will be treated with the A2/4-1BBL melanoma vaccine, a compatible melanoma cell line that has been engineered to express a molecule termed 4-1BBL, which enhances the chances of the cell line to be recognized by the patient's immune system, and to induce its stimulation. The hypothesis that drives the study states that the immune response against the cell line will also be effective against the residual tumor that may still be present in the body.
Key facts
- Study ID
- NCT01898039
- Run by
- Hadassah Medical Organization
- People needed
- 50
- Starts
- 2013-05-01
- Expected to finish
- 2027-04-01
- Last updated by the study team
- 2025-10-02
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients included in this protocol must carry one or more of the following tissue typing alleles: HLA-A2, -A24, -A33, -B35, -B49, -CW04/12(04/08). We estimate that 50% of melanoma patients will be eligible.
- Cutaneous malignant melanoma AJCC stage IIb (>4 mm) or IIc (ulcerated melanoma >4mm).
- Metastatic melanoma AJCC stage III (nodal involvement, N1-3a,b) post-surgical removal of lymph nodes.
- Metastatic melanoma AJCC stage IV, completely resected.
- Non-resectable metastatic melanoma of low burden disease and normal LDH who have undergone at least two treatment lines, including chemotherapy (DTIC, temodal, taxanes, platinum compounds), anti-CTLA-4 (ipilimumab) and B-RAF inhibitor if harboring the V600E BRAF mutation in their tumor.
- Non cutaneous malignant melanoma of respective stages including uveal and mucosal melanoma.
- Melanoma can be of either mutant or wild-type B-RAF.
- Karnofsky performance status > 80 (Normal activity with effort).
- No active cardio-respiratory disease.
- Not pregnant or nursing. Women must take contraceptives during the treatment period.Hematocrit >25% and WBC >3000.
- Informed consent of the patient.
You may not qualify if…
- Administration of cytotoxic drugs or extensive radiotherapy less than 28 days prior to protocol administration.
- Active brain metastases requiring corticosteroids.
- Concurrent malignancy (other than skin cancer, carcinoma in situ of cervix and early stage prostate cancer).
- Active serious infection.
- Allergy to penicillin.
- Patient's will to withdraw from the study at any stage.
- HIV and chronic hepatitis B and C carrier
Where it is running
- Sharett Institute of Oncology, Hadassah Medical Organization — Jerusalem, Israel (enrolling)
Full record on ClinicalTrials.gov
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