Clinical trial · Interventional
Active Specific Intranodal Immunotherapy of Recombinant Vaccinia Virus in Locally Advanced to Metastatic Melanoma
Active Specific Intranodal Immunotherapy With a Recombinant Vaccinia Virus Expressing Three Melanoma Associated Epitopes and Two Costimulatory Molecules, Followed by Immunization With Synthetic Melanoma Associated Epitopes. A Phase I/II Trial in Patients With Stages IIb to 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)
The purpose of this study is to assess intranodal immunotherapy in locally advanced to metastatic melanoma patients (American Joint Committee on Cancer \[AJCC\] stages IIb to IV). For this, the investigators capitalize on their previous melanoma clinical trial (published by Zajac P et al in Human Gene Ther 2003) and take advantage of a proprietary recombinant vaccinia virus (replication inactivated) expressing 5 minigenes: 3 melanoma associated antigens and 2 costimulatory molecules. Immunization with the recombinant vaccinia virus is followed by 3 boosts with soluble, synthetic melanoma associated antigens. The patients are immunized intranodally (groin lymph node) under ultrasonographic guidance in an outpatient clinic. The protocol foresees 2 cycles of immunotherapy for alternate weeks and lasts 15 weeks.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Melanoma | Melanoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Intranodal booster immunizations with synthetic melanoma associated epitopes | Biological | — | UNRESOLVED |
| Intranodal immunization with a recombinant vaccinia virus expressing 5 transgenes | Genetic | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (3)
- measure
- Safety evaluation
- measure
- Clinical response
- measure
- Immune response assessment
Secondary outcomes (2)
- measure
- Survival (disease-free survival [DFS], overall survival [OS])
- measure
- Dose adaptation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients older than 18 years * Histologically proven melanoma in AJCC stages IIb to IV * Resected, recurrent or disseminated disease * HLA-A2.1 MHC phenotype * Karnofsky performance status equal or higher than 70% Exclusion Criteria: * Patients younger than 18 years * Pregnancy or inability to perform anticonception * MHC phenotype other than HLA-A2.1 * Other concurrent malignant disease * Estimated life expectancy of less than 6 months * Allergic skin diseases, including eczema, psoriasis and neurodermitis * Fever or active infection of the respiratory system * Concurrent severe cardiac or pulmonary disease (New York Heart Association \[NYHA\] III and IV) * Significant impairment of liver or kidney function (bilirubin \> 30umol/l, GOT \>2.5xN, GPT \>2.5xN, alkaline phosphatase \>2.5xN, creatinine \>1.5xN adapted to the age) * Impairment of the immune system (leucocyte counts \<3000/mm3 or granulocytes counts \<1500/mm3) * Concurrent immunosuppressive therapy * Preexisting severe anemia (hemoglobin lower than 80 g/l) * Preexisting thrombocytopenia (platelet counts lower than 75,000/ul) * Ongoing chemotherapy or chemotherapy completed less than 6 weeks before enrollment in the trial * Any medical or psychiatric condition which, in the opinion of the treating physician or principal investigator, would unacceptably reduce the safety of the proposed treatment, would impair the delivery of treatment, or would preclude obtaining voluntary informed consent * Patients receiving any other concurrent investigational treatment, or any other concurrent treatment for their cancer * Patients who cannot avoid close contact with children less than 3 years of age or with immunocompromised household members
References
Publications (6)
- BACKGROUNDSpagnoli GC, Zajac P, Marti WR, Oertli D, Padovan E, Noppen C, Kocher T, Adamina M, Heberer M. Cytotoxic T-cell induction in metastatic melanoma patients undergoing recombinant vaccinia virus-based immuno-gene therapy. Recent Results Cancer Res. 2002;160:195-201. doi: 10.1007/978-3-642-59410-6_23. PMID 12079214
- BACKGROUNDZajac P, Schutz A, Oertli D, Noppen C, Schaefer C, Heberer M, Spagnoli GC, Marti WR. Enhanced generation of cytotoxic T lymphocytes using recombinant vaccinia virus expressing human tumor-associated antigens and B7 costimulatory molecules. Cancer Res. 1998 Oct 15;58(20):4567-71. PMID 9788602
- BACKGROUNDAdamina M, Oertli D. Antigen specific active immunotherapy: lessons from the first decade. Swiss Med Wkly. 2005 Apr 16;135(15-16):212-21. doi: 10.4414/smw.2005.10127. PMID 15971113
- RESULTZajac P, Oertli D, Marti W, Adamina M, Bolli M, Guller U, Noppen C, Padovan E, Schultz-Thater E, Heberer M, Spagnoli G. Phase I/II clinical trial of a nonreplicative vaccinia virus expressing multiple HLA-A0201-restricted tumor-associated epitopes and costimulatory molecules in metastatic melanoma patients. Hum Gene Ther. 2003 Nov 1;14(16):1497-510. doi: 10.1089/104303403322495016. PMID 14577912
- RESULTOertli D, Marti WR, Zajac P, Noppen C, Kocher T, Padovan E, Adamina M, Schumacher R, Harder F, Heberer M, Spagnoli GC. Rapid induction of specific cytotoxic T lymphocytes against melanoma-associated antigens by a recombinant vaccinia virus vector expressing multiple immunodominant epitopes and costimulatory molecules in vivo. Hum Gene Ther. 2002 Mar 1;13(4):569-75. doi: 10.1089/10430340252809856. PMID 11874634
- RESULTAdamina M, Rosenthal R, Weber WP, Frey DM, Viehl CT, Bolli M, Huegli RW, Jacob AL, Heberer M, Oertli D, Marti W, Spagnoli GC, Zajac P. Intranodal immunization with a vaccinia virus encoding multiple antigenic epitopes and costimulatory molecules in metastatic melanoma. Mol Ther. 2010 Mar;18(3):651-9. doi: 10.1038/mt.2009.275. Epub 2009 Nov 24.