Vaccine Tested in Adults with Acute Myeloid Leukemia in Remission

Trial details

Who runs it

University Hospital Tuebingen

Trial code

NCT06252584

Record updated

9 November 2026

Original description

The aim of this Phase I study is to evaluate the immunogenicity along with safety and toxicity as well as first efficacy of a multi-peptide vaccine adjuvanted with the TLR1/2 ligand XS15 emulsified in Montanide ISA 51 VG (AML-VAC-XS15) in AML patients who have achieved CR or CRi with first line treatment.Read full original descriptionShow less

Multi-peptide Vaccination Adjuvanted With the TLR1/2 Ligand XS15 in Acute Myeloid Leukemia (AML) Patients Who Have Achieved Complete Remission With First Line Therapy

The aim of this Phase I study is to evaluate the immunogenicity along with safety and toxicity as well as first efficacy of a multi-peptide vaccine adjuvanted with the TLR1/2 ligand XS15 emulsified in Montanide ISA 51 VG (AML-VAC-XS15) in AML patients who have achieved CR or CRi with first line treatment.

Inclusion: Males or females aged ≥18 years of age; Existence of a written informed consent; Documented diagnosis of AML according to WHO guidelines; morphological complete remission (CR) or complete remission with incomplete blood count recovery (CRi); positive MRD is permitted; completion of previous intensive therapy (first vaccination 4-28 weeks after last application of chemotherapy) or; ongoing low intensity treatment with e.g. hypomethylating agents (HMA), venetoclax, etc; ongoing maintenance treatment with e.g. oral azacytidine or midostaurin is permitted; not eligible for allogeneic stem cell transplantation; Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 2; Adequate organ function laboratory values; bilirubin ≤ 3 times upper limit range (exception isolated indirect hyperbilirubinemia (Morbus Gilbert-Meulengracht)); alanine aminotransferase (ALT) and aminotransferase (AST), ≤ 5 times upper limit range; creatinine clearance GFR > 30 ml/min (CKD-EPI); platelets > 50.000/μl; absolute CD3+ T cell count ≥ 200/μl; negative serological hepatitis B test or negative PCR in case of positive serological test without evidence of an active infection, negative testing of hepatitis C RNA, negative HIV test within 6 weeks prior to study inclusion; Female patients of child bearing potential (FCBP) and male patients with partners of child bearing potential, who are sexually active, must agree to the use of two effective forms (at least one highly effective method) of contraception (for more detailed information see chapter 5.7 Contraception, pregnancy, sperm donation and nursing). This should be started from the signing of the informed consent and be continued until 3 months (both female and male patients) after last vaccination); For FCBP two negative pregnancy tests (sensitivity of at least 25 mlU/mL) prior to first application of first vaccination, one at screening and the other prior (< 24 h) to first vaccination; Postmenopausal or evidence of non-child-bearing status.

Exclusion: Chemotherapy or other systemic therapy or radiotherapy, up to 14 days prior to the first dose of study drug (ongoing maintenance treatment or low intensity treatment is permitted); Concurrent or previous treatment within 28 days in another interventional clinical trial with an investigational anticancer therapy or any other investigational therapy, which would interfere with the study's primary and secondary endpoints; Major surgery within 28 days of dosing of study drug; Treatment with immunotherapy agents within 28 days of dosing of study drug; Autoimmune disease that requires or has required treatment with systemic immunosuppressive treatments, except low dose corticosteroids (< 10 mg/ day), in the past 1 year; Prior stem cell allograft or organ transplantation; Have received any live vaccination within 28 days prior to the first dose of AML-VAC-XS15; Ongoing or active infection (including SARS-CoV-2); Prior history of malignancies, other than AML/myelodysplastic syndrome (MDS), unless the subject has been free of the disease for; ≥ 2 years. Exceptions include the following: basal cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, histological finding of prostate cancer of TNM stage T1; Pregnant or breastfeeding; Unwilling or unable to follow the study schedule for any reason; Diagnosis of acute promyelocytic leukemia (APL).

ClinicalTrials.gov NCT06252584