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Antisecretory Factor in Primary Glioblastoma 1

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

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04116138
Acronym
AFGBM1
Enrollment
8
Registered
2019-10-04
Start date
2019-09-01
Completion date
2021-03-31
Last updated
2021-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Edema, Chemotherapy Effect, Glioblastoma

Brief summary

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.

Detailed description

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.

Interventions

DIETARY_SUPPLEMENTSalovum

Egg yolk powder enriched for anti secretory factor

Sponsors

Region Skane
CollaboratorOTHER
Lund University
CollaboratorOTHER
Skane University Hospital
CollaboratorOTHER
Lantmannen Medical AB
CollaboratorOTHER
Peter Siesjö
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Phase 1-2, open label, single arm, single center.

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
No

Inclusion criteria

1. Pathology verified glioblastoma 2. Age 18-69 years 3. Surgical treatment-biopsy or resection. 4. Scheduled full concomitant radiochemotherapy treatment with radiation (60 Gy) and temozolomide, 5. Informed consent

Exclusion criteria

1. No informed consent 2. Egg yolk allergy

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with treatment-related adverseCumulative from day 1 to 80Treatment related adverse events as assessed by CTCAE v 5.0
Number of participants with completion of prescribed Salovum treatmentCumulative from day 1 to 80Defined as completing prescribed full Salovum treatment

Secondary

MeasureTime frameDescription
Number of participants with reduced or no steroid intakeChange 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.
Number of participants with altered blood levels of triglycerides and cholesterolChange from baseline at day 20, 57 and 70.Blood levels of triglyceride and cholesterol above normal range or increased from baseline
Number of participants with detetable blood levels antisecretory factorChange from baseline at day 20, 57 and 70.Analysis of anti secretory factor-16 (AF-16) blood levels by enzyme linked immunoassay
Number of participants with altered blood levels of inflammatory cytokinesChange 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

MeasureTime frameDescription
Number of participants with decreased performanceChange 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)
Number of participants with decreased quality of lifeChange 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
Number of participants with decreased neurological functionChange 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)
Cognitive functionChange from baseline at day 20, 57 and 70.Number of participants with decreased cognitive function assessed by Mini Mental State Examination (MMSE)

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026