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Status unknownNCT04145232Updated Aug 10, 2020

AImmune - Artificial Intelligence Algorithm for Identification of Immunogenic Neoepitopes of Cancer to Predict and Boost Patient's Response to Immunotherapies.

An observational study in Non Small Cell Lung Cancer, Neoepitopes and Neoantigens, sponsored by Ardigen. Status unknown at 1 site in Poland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-08-10.

Sponsored by Ardigen · Observational

The sponsor has not verified this record recently (last verified Aug 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
30
Ages
18 Years and older
Sex
All
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Study summary

The goal of the project is to develop and validate A.I.mmune technology. It performs complex analyses of patients' tumor and immune system state using data derived from next-generation sequencing of tumor and healthy tissue to identify cancer neoantigens, which are likely to elicit an immune response.

A key challenge to be solved using the technology is to predict for each patient which neoepitopes are not only likely to bind to HLA or be presented on the tumor cell surface, but also will be recognized by the T-cell receptor and create the immunogenic response. The presence of such epitopes is required for immunotherapy by immune checkpoint inhibition to have an effect on the disease. Knowledge of those epitopes enables therapeutic strategies to boost the immune response by designing personalized cancer vaccines and adoptive cell therapies.

The samples and data collected in this clinical study will be used for clinical validation of A.I.mmune technology. For all patients treated with immunotherapy (using anti-PD1 / anti-PDL1 and / or anti-CTLA-4 antibodies) peripheral blood samples (PBMC) and biopsy (FFPE) collection will be performed before treatment. Samples will be sequenced by next-generation sequencing platform. In parallel, the investigators will also collect samples of stool (one sample before the start of immunotherapy) and follow-up information of responses to treatment.

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Conditions studied

  • Non Small Cell Lung Cancer
  • Neoepitopes
  • Neoantigens
  • Immunotherapy
  • Next Generation Sequencing (NGS)
  • Personalized Neoantigen Cancer Vaccine

Keywords

  • Cancer
  • Non Small Cell Lung Cancer
  • Neoepitopes
  • Neoantigens
  • Immunotherapy
  • Nivolumab
  • Ipilimumab
  • Atezolizumab
  • Neoantigen cancer vaccine
  • Personalized neoantigen cancer vaccine
  • FFPE
  • PBMC
  • Stool
  • Immuno-Oncology
  • Next generation sequencing (NGS)
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In context

Carcinoma, Non-Small-Cell Lung

6,485 studies on the registry are indexed under Carcinoma, Non-Small-Cell Lung; 1,630 are open to participants now.

This study's planned enrollment of 30 is below the median of 161 across 948 observational studies indexed under Carcinoma, Non-Small-Cell Lung.

Browse Carcinoma, Non-Small-Cell Lung studies →

Lead sponsor

Ardigen is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients receiving routine treatment.

Inclusion criteria

  • Men or women ≥18 years of age.
  • Patients with non-small cell lung cancer.
  • Patients with informed consent to participate in the study.
  • Patients receiving routine treatment (immunotherapy using anti-PD1 / anti-PDL1 and / or anti CTLA4 antibodies), financed by the Polish National Health Fund (NFZ).
  • The applied immunotherapy should be the first or second line of treatment.

Exclusion criteria

Exclusion Criteria:

  • Patients who are unable to understand, read and / or sign informed consent.
  • Patients who can not collect stools.
  • Patients with fecal transplant.
  • The applied immunotherapy is not the first or second line of treatment.
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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
30 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • NSCLC

    This cohort will consist of 30 patients with non-small cell lung cancer (NSCLC).

    Biological: Collection of biopsy (FFPE), blood (PBMC) and stool

Interventions

  • BiologicalCollection of biopsy (FFPE), blood (PBMC) and stool

    Patients receiving routine treatment (immunotherapy using anti-PD1 / anti-PDL1 and / or anti CTLA4 antibodies), financed by the Polish National Health Fund (NFZ).

    Also known as: Nivolumab, Ipilimumab, Atezolizumab

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What researchers measure

Primary outcomes

  1. Number of Responders and Non-responders on immunotherapy (evaluated using RECIST 1.1 criteria)

    Standard follow-up care after cancer treatment.

    Time frame: Up to 6 months

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Study locations

1 of 1 sites recruiting
  • University Clinical Centre in Gdansk
    Gdańsk, Poland
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 10, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04145232
Lead sponsor
Ardigen
Collaborators
Małopolskie Centre of Entrepreneurship
Responsible party
Sponsor
First posted
Oct 30, 2019
Start date
Jun 13, 2019
Primary completion
Oct 15, 2020 (estimated)
Completion
Nov 30, 2020 (estimated)
Last update
Aug 10, 2020

Study contacts

Martyna Balawejder
Contact
martyna.balawejder@ardigen.com
+48 883 319 890
Bozena Augustyn
Contact
bozena.augustyn@ardigen.com
+48 12 340 94 94
Piotr Stepniak
principal investigator · Ardigen

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

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