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Completed

NCT Number: NCT04335890

IKKb-matured, RNA-loaded Dendritic Cells for Metastasised Uveal Melanoma

A Phase I vaccination trial in patients suffering from recently diagnosed metastatic uveal melanoma not cureable with local therapy and needing systemic therapy. IKKb-matured Dendritic Cells loaded with autologous tumor-RNA + RNA coding for defined antigens and driver mutations will be added to a standard therapy chosen by the tumor board (either checkpoint blockade or chemotherapy).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University Hospital Erlangen Dept. of Dermatology

Erlangen, Bavaria, 91054, Germany

About this study

Intravenous infusion of 7.5 to 30 mio DCIKKb at 9 vaccination time points (week 1, 3, 7, 13, 19, 25, 31, 37 and 42) and in intervals of 2, 4, and 6 intervals of 6 weeks) is scheduled; the first 4 patients will receive reduced doses for the first 4 vaccinations, namely 7.5 mio (1st and 2nd vaccination) and 15 mio (3rd and 4th vaccination) DC followed by the full dose of 30 mio for subsequent vaccinations. Patients number 5 to 8 will receive initially reduced doses of 15 mio (1st and 2nd vaccination) DC for the first 2 vaccinations, and the full dose of 30 mio for subsequent vaccinations. Patients number 8 to 12 will receive the full dose of 30 mio cells from vaccination 1 onwards provided that no major side effects occurred. Patients will be vaccinated in a staggered approach by selectively decelerating release of the vaccine.

DCIKKb = autologous, monocyte-derived DC that are matured with the standard cocktail (TNF-alpha, IL-1 beta, IL-6 and PGE2) and IKKb-RNA loaded by electroporation with 1) autologous PCR-amplified total tumor mRNA, 2) RNA coding for defined tumor associated antigens (TAA) namely gp100, tyrosinase, PRAME, MAGE-A3, IDO) and 3) RNA coding for driver mutations (GNAQ/GNA11Q209 or R183, or the less frequently occurring SF3B1R625, CYSLTR2L129Q or PLCB4D630) by electroporation; RNAs for selected TAAs are in stock and will be transfected into the DCs only if expressed in the individual tumor of a patient (shown by RNA sequencing of the tumor); RNAs for selected driver mutations are in stock and will be loaded into the DCs only if the respective mutation is found (proven by exome and RNA sequencing) in the individual tumor.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed unresectable stage IV metastatic uveal melanoma as per AJCC staging system 2014, 7th edition (updated 2018) not curable with local therapy modalities
  • WHO performance status of 0, 1 or 2
  • age from 18 and ≤ 75 years
  • negative pregnancy test
  • signed informed consent

Exclusion criteria

  • Major serious illness
  • evidence for HIV-1, HIV-2, HTLV-1, HBV or HCV infection
  • active autoimmune disease requiring immunosuppressive therapy
  • splenectomy or radiation therapy of the spleen
  • organ allografts
  • pregnancy
  • lactation
  • psychiatric disorders
  • severe organic brain syndrome

Treatment and study plan

Vaccination with IKKb matured Dendritic Cells

Biological

IKKb matured autologous monocyte derived dendritic cells loaded with RNAs; intravenous Infusion with a dose escalation starting with 7.5 mio Dendritic Cells for the first vaccination up to 30 mio cells per vaccination

Other names: Dendritic Cell vaccine

Primary outcomes

  1. Safety of DCIKKb

    Time frame: 1 year

    Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)

  2. Tolerability of DCIKKb

    Time frame: 1 year

    Assesment of Quality of life using Quality of life EORTC QLQ-C30, Version 2

  3. Dose-limiting toxicities (DLTs) of DCIKKb

    Time frame: 1 year

    Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)

  4. Maximum tolerated dose (MTD) of DCIKKb

    Time frame: 1 year

    Assesment of side effects using the Common Toxicity Criteria (CTC v4.0)

Secondary outcomes

  1. Prolongation of median overall survival

    Time frame: 2 years

    Assesment of survival

  2. Prolongation of overall survival (OS) after 1 and 2 years

    Time frame: 2 years

    Assesment of survival

  3. Induction of antigen specific CD8+ T cells and / or CD4+ T cells against TAA and mutated drivers

    Time frame: 2 years

    Assesment of immune responses

Sponsors and collaborators

Lead sponsor

Hasumi International Research Foundation

Other

Registry information

Official study title

Phase I Vaccination Trial in Metastatic Uveal Melanoma Using IKKb-matured Dendritic Cells Loaded With Autologous Tumor-RNA + RNA Coding for Defined Antigens and Driver Mutations

Important dates

Study start
2020
Primary completion
2022
Study completion
2024
First posted
Apr 7, 2020
Registry last updated
Mar 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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