Clinical trial · Interventional
Monoclonal Antibody and Vaccine Therapy in Treating Patients With Stage III or Stage IV Melanoma That Has Been Removed During Surgery
An Open-label Study Of MDX-CTLA4 In Combination With Tyrosinase/gp100/MART-1 Peptides Emulsified With Montanide ISA 51 In The Treatment Of Patients With Resected Stage III Or Stage IV Melanoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Monoclonal antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Vaccines made from a person's cancer cells may make the body build an immune response to kill tumor cells. PURPOSE: Phase I trial to study the effectiveness of combining monoclonal antibody therapy and vaccine therapy in treating patients who have stage III or stage IV melanoma that has been removed during surgery.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Intraocular Melanoma | Uveal Melanoma | ALIAS | 0.90 |
| Melanoma (Skin) | Melanoma | ONTOLOGY_EXACT | 0.85 |
Interventions
Interventions (6)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| adjuvant therapy | Procedure | — | UNRESOLVED |
| gp100 antigen | Biological | — | UNRESOLVED |
| incomplete Freund's adjuvant | Biological | — | UNRESOLVED |
| ipilimumab | Biological | Ipilimumab | ALIAS |
| MART-1 antigen | Biological | — | UNRESOLVED |
| tyrosinase peptide | Biological | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically confirmed completely resected stage III or IV melanoma * Mucosal or ocular subtypes allowed * HLA-A2 positive * Positive staining of tumor tissue with antibody HMB-45 for gp100, tyrosinase, and/or MART-1 * Failed (or ineligible for or refusal of) interferon alfa PATIENT CHARACTERISTICS: Age: * Not specified Performance status: * Karnofsky 60-100% Life expectancy: * At least 12 months Hematopoietic: * WBC at least 2,500/mm\^3 * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 * Hemoglobin at least 10 g/dL * Hematocrit at least 30% Hepatic: * Bilirubin no greater than upper limit of normal (ULN) * AST no greater than 1.25 times ULN * Hepatitis B surface antigen negative * Hepatitis C antibody nonreactive Renal: * Creatinine less than 1.25 times ULN Immunologic: * Antinuclear antibody (ANA) negative OR * If ANA positive, must be: * Antithyroglobulin antibody negative * Rheumatoid factor negative * Anti-LKM antibody negative * Anti-phospholipid antibody negative * Anti-islet cell antibody negative * Anti-neutrophil cytoplasmic antibody negative * HIV negative * No autoimmune disease (e.g., uveitis or autoimmune inflammatory eye disease) * No active infection * No hypersensitivity to tyrosinase:368-376, gp100:209-217, MART-1:26-35, or Montanide ISA-51 Other: * No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the cervix * No underlying medical condition that would preclude study * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * See Disease Characteristics * No prior anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody * No prior tyrosinase, gp100, or MART-1 peptide * No prior antitumor vaccination * No prior interleukin-2 * At least 4 weeks since prior immunotherapy for melanoma Chemotherapy: * At least 4 weeks since prior chemotherapy for melanoma Endocrine therapy: * At least 4 weeks since prior hormonal therapy for melanoma * At least 4 weeks since prior corticosteroids * No concurrent systemic or topical corticosteroids Radiotherapy: * At least 4 weeks since prior radiotherapy for melanoma Surgery: * See Disease Characteristics Other: * No prior cytotoxic therapy * At least 4 weeks since any other prior therapy for melanoma * Concurrent analgesics allowed if on stable dose for at least 2 weeks before study
References
Publications (0)
Data not yet available