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OpenTrials
Completed

NCT Number: NCT03381768

Peptide Vaccination Against PD-L1 and PD-L2 in Relapsed Follicular Lymphoma

An open phase-1, first-in-human, clinical trial investigating the safety and immunological effects of peptide vaccination with Programmed Death Ligand 1 and 2 (PD-L1 and PD-L2) peptides in patients with relapsed follicular lymphoma.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Herlev Hospital

Herlev, RegionH, 2730, Denmark

About this study

Follicular lymphoma (FL) is the the most common of the indolent lymphomas, with an incidence in Denmark of 220 per year. In 90% of the cases the disease is incurable why the treatment strategy often is watchful waiting until significant signs of progression or transformation. After chemotherapy, maintenance therapy is often used to increase disease control.

The microenvironment and immune escape mechanism are believed to play a major role in the persistence of the lymphoma. One escape mechanism is the PD-L1 and PD-L2 molecules expressed in the microenvironment of follicular lymphoma inhibiting the T-cells. By stimulating the T-cells to attack PD-L1 and PD-L2 expressing cells we hope to hamper the immunosuppressive tumor environment and establish immune tumor control.

10 patients treated with standard therapy are needed for the trial and each patient will receive 15 vaccinations over the course of one year.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically documented FL grade I-IIIa, with no sign of current transformation. Patients cured of transformed lymphoma are eligible.
  • A minimum of one line of induction therapy. Maintenance rituximab can continue along with the vaccination
  • At least partial response to the latest standard treatment
  • A minimum of 4 weeks since last treatment
  • Age ≥ 18
  • ECOG performance status of 0 or 1
  • Life expectancy ≥ 12 weeks
  • Adequate hematologic and end-organ function

Exclusion criteria

  • Progression with the presence of at least one GELF criteria or transformation at inklusion time.
  • Other active malignant diseases
  • Significant medical condition per investigators judgement e.g. severe Asthma/COLD, poorly regulated heart condition, insulin dependent diabetes mellitus.
  • Acute or chronic viral/bacterial infection e.g. HIV, CMV, EBV, hepatitis or tuberculosis
  • Serious known allergies or earlier anaphylactic reactions.
  • Known sensibility towards Montanide ISA-51
  • Any active autoimmune diseases e.g. autoimmune neutropenia, thrombocytopenia or hemolytic anemia, systemic lupus erythematosus, scleroderma, myasthenia gravis, autoimmune glomerulonephritis, autoimmune adrenal deficiency, autoimmune thyroiditis etc.
  • Pregnancy

Treatment and study plan

PD-L2 peptide

Biological

100 ug PD-L2 peptide dissolved in DMSO and water mixed with 500ul montanide.

PD-L2 and PD-L1 peptide

Biological

100 ug PD-L2 peptide and 100ug PD-L1 peptide dissolved in DMSO and water mixed with 500ul montanide.

Primary outcomes

  1. Adverse events evaluated by CTCAE 4.03

    Time frame: 1 year follow up

    Adverse events are graded 1-5 according to the criteria

Secondary outcomes

  1. Immune responses

    Time frame: 1 year

    T-cell cytokine release towards target antigens

Other outcomes

  1. Clinical response according to Lugano criteria

    Time frame: 1 year

    Changes in tumor size on CT

  2. Clinical response according to Lugano criteria

    Time frame: 1 year

    Changes in tumor metabolism on PET

  3. Minimal residual disease

    Time frame: 1 year

    measured by circulating tumor DNA

Sponsors and collaborators

Lead sponsor

Lars Møller Pedersen

Other

Registry information

Official study title

PD-L1 and PD-L2 Peptide Vaccination as Consolidation for Relapsed Follicular Lymphoma

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Dec 22, 2017
Registry last updated
Feb 24, 2021

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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