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Antisecretory Factor Glioblastoma Phase 2

Antisecretory Factor During Concomitant and Adjuvant Therapy of Primary Glioblastoma, a Randomised, Prospective and Double Blinded Study

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05669820
Acronym
AFGB2
Enrollment
300
Registered
2023-01-03
Start date
2024-01-15
Completion date
2027-12-01
Last updated
2026-01-09

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

Conditions

Glioblastoma

Keywords

Antisecretory factor, Trials, Randomized Clinical

Brief summary

This is a randomised, double blinded and multiple center , Phase 2 study in patients with newly diagnosed glioblastoma. Participants will receive an egg powder enriched for antisecretory factor (AF), Salovum, or a placebo egg powder daily from 2 days before concomitant radio-chemo therapy or chemotherapy until 14 days after finalisation plus during adjuvant chemotherapy.The primary aims of are overall survival at 6 and 12 months after diagnosis

Detailed description

Glioblastoma (GB) 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 with antisecretory and anti-inflammatory effects. 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 an din other countries. 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. 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. Intratumoral delivery of AF-16 potentiated the effect of intratumoral temozolomide in an experimental model of glioblastoma. 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. In a completed phase1-2 trial in participants with primary gliobalstoma the add on of Salovum during concomitant radiochemotherapa was considered safe and feasible. The current study is aimed at assessing the efficacy of Salovum in a RCT (randomised controlled trail).

Interventions

DIETARY_SUPPLEMENTSalovum

Salovum is an eggyolkpowder derived from hens fed with SPC (specially processed cereals) and contains increased amounts of the endogenous protein antisecretory factor.

DIETARY_SUPPLEMENTPlacebo egg yolk powder

Egg yolk powder derived from hen fed with normal feed.

Sponsors

Lund University
CollaboratorOTHER
Peter Siesjö
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Eggyolk powder with same smell, texture and colour in identical packages.

Intervention model description

Randomized, prospective, double blinded

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Pathology verified glioblastoma or astrocytoma grade 4 2. Age 18-75 years 3. Surgical treatment-resection. 4. Scheduled concomitant radiochemotherapy, or only chemotherapy. 5. Informed consent

Exclusion criteria

1. No informed consent 2. Egg yolk allergy 3. Only surgical biopsy 4. Only radiotherapy

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalup to 12 months from primary surgerySurvival

Secondary

MeasureTime frameDescription
Progress free survival at 6 and 12 monthsAt 6 and 12 months from primary surgeryProgress free survival as a compound assessment by a multidisciplinary conference (MDC)

Other

MeasureTime frameDescription
QOL Assessed by European Organization of Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C30up to 1 yearsAssessed by European Organization of Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C30 questionnaire
Cognitive functionup to 1 yearAssessed by Montreal Cognitive Assessment (MoCA)
Performance Assessed by Eastern Oncology Cooperative Group (ECOG) performance scaleup to 1 yearAssessed by Eastern Oncology Cooperative Group (ECOG) performance scale
quality of life (QOL) assessed by brain cancer module (BN20) questionnaireup to 1 yearsAssessed by brain cancer module (BN20) questionnaire
Neurological functionup to 1 yearAssessed by Neurologic Assessment in Neuro-Oncology (NANO) scale

Countries

Sweden

Contacts

Primary ContactPeter Siesjö, MD, PhD
peter.siesjo@med.lu.se+4646171274
Backup ContactJohan Bengzon, MD, PhD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026