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NCT Number: NCT04116138

Antisecretory Factor in Primary Glioblastoma 1

This is a non-randomised, open-label, single center-centre, Phase I-II study in patients with newly diagnosed glioblastoma. 5 patients with newly diagnosed glioblastoma are enrolled in the study and will receive an egg powder enriched for antisecretory factor (AF), Salovum, daily from 2 days before concomitant radio-chemo therapy until 14 days after finalisation.The primary aim of the study is to asses safety and feasibility of this regimen.

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Key information

About this study

Glioblastoma (GBM) is the most common primary brain tumor and also has the worst prognosis with a mean survival time below 1 year and a 5-year survival rate of less than 2%.

AF is a 41kilodalton endogenous and essential protein encompassing antisecretory and anti-inflammatory effect. Endogenous AF activity increases after exposure to bacterial toxins and endogenous triggers of inflammation. The active amino-terminal portion of AF has been synthesized as a 16 amino acid peptide (AF-16) and has been used in animal experimental studies. Salovum® is a product based on egg yolk powder B221® and contains high levels of AF. Salovum® is classified as food for special medicinal purposes (FSMP) by the European Union.

Many tumors show elevated interstitial fluid pressure (IFP) compared to the surrounding tissue due to vascular leakage, providing a barrier for drug uptake in solid tumors, as well as poor perfusion, resulting in hypoxia and relative resistance to radiochemotherapy.

In a mouse model of malignant brain tumor, preliminary findings show that intratumoral infusion of AF-16 greatly enhances the effect of simultaneous intratumoral temozolomide treatment (90% and 40% survival, respectively). AF-16 also has preliminarily significant immune modulatory effects on myeloid cells in vitro, but also effects on the secretion of immune modulatory agents from tumor cells. AF-16 was reported to significantly reduce the IFP in xenotransplanted human glioblastoma by inhibiting an ionic pump, NKCC1, in the tumor tissue. Both Salovum® and AF-inducing specific processed cereals (SPC) prolonged survival in the same models. Systemic temozolomide treatment combined with AF inducing SPC completely blocked tumor growth in GBM xenografts. Likewise, SPC treatment abrogated 90% of pre-established syngeneic tumors in immune competent animals.

Mechanistically, it remains unclear whether AF's effect in tumor models is mediated through decrease of IFP and/or immunomodulation. Also, an effect on the complement system through modulation of circulating complement complexes with proteasome units has been proposed.

Salovum® has been administered to patients with various diseases as, inflammatory bowel disease, Mb Ménière and mastitis and traumatic brain injury without signs of any adverse effects.

The described study is a safety and feasibility study and if these criteria are fulfilled, will be followed by a randomised controlled trial.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pathology verified glioblastoma
  • Age 18-69 years
  • Surgical treatment-biopsy or resection.
  • Scheduled full concomitant radiochemotherapy treatment with radiation (60 Gy) and temozolomide,
  • Informed consent

Exclusion criteria

  • No informed consent
  • Egg yolk allergy

Treatment and study plan

Salovum

Dietary Supplement

Egg yolk powder enriched for anti secretory factor

Other names: Antisecretory factor

Primary outcomes

  1. Number of participants with treatment-related adverse

    Time frame: Cumulative from day 1 to 80

    Treatment related adverse events as assessed by CTCAE v 5.0

  2. Number of participants with completion of prescribed Salovum treatment

    Time frame: Cumulative from day 1 to 80

    Defined as completing prescribed full Salovum treatment

Secondary outcomes

  1. Number of participants with altered blood levels of triglycerides and cholesterol

    Time frame: Change from baseline at day 20, 57 and 70.

    Blood levels of triglyceride and cholesterol above normal range or increased from baseline

  2. Number of participants with reduced or no steroid intake

    Time frame: Change from baseline at day 7, 14, 21, 28, 35, 42, 49, 56, 63 and 70.

    Intake of oral corticosteroids assessed weekly during and after intervention.

  3. Number of participants with detetable blood levels antisecretory factor

    Time frame: Change from baseline at day 20, 57 and 70.

    Analysis of anti secretory factor-16 (AF-16) blood levels by enzyme linked immunoassay

  4. Number of participants with altered blood levels of inflammatory cytokines

    Time frame: Change from baseline at day 20, 57 and 70.

    Analysis of interleukin-6 (IL-6), interleukin- (IL-8), monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory protein-1a (MIP-1a), macrophage inflammatory protein-1b (MIP-1b) by multiplex analysis

Other outcomes

  1. Cognitive function

    Time frame: Change from baseline at day 20, 57 and 70.

    Number of participants with decreased cognitive function assessed by Mini Mental State Examination (MMSE)

  2. Number of participants with decreased neurological function

    Time frame: Change from baseline at day 20, 57 and 70.

    Neurologic function assessed by Neurologic Assessment in Neuro-Oncology (NANO) scale. Minimum 0 (no deficits) and maximum 25 (maximum deficits)

  3. Number of participants with decreased performance

    Time frame: Change from baseline at day 20, 57 and 70.

    Number of participants with decreased performance assessed by Eastern Oncology Cooperative Group (ECOG) scale. Minum 0 (normal function) and maximum 4 (maximum disability)

  4. Number of participants with decreased quality of life

    Time frame: Change from baseline at day 20, 57 and 70.

    Number of participants with decreased quality of life assessed by European Organization of Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C30 and brain cancer module (BN20) questionnaire

Sponsors and collaborators

Lead sponsor

Peter Siesjö

Other

Collaborators

  • Lantmannen Medical AB
  • Lund University
  • Region Skane
  • Skane University Hospital

Registry information

Official study title

Antisecretory Factor, Administered as an Enriched Egg Powder, Salovum®, as Supplementary Therapy for Primary Glioblastoma During Concomitant Radio-chemotherapy.

Acronym: AFGBM1

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Oct 4, 2019
Registry last updated
Apr 28, 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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