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Antisecretory Factor Glioblastoma Phase 2 (AFGB2)

Primary Purpose

Glioblastoma

Status
Recruiting
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Salovum
Placebo egg yolk powder
Sponsored by
Peter Siesjö
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma focused on measuring Antisecretory factor, Trials, Randomized Clinical

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Pathology verified glioblastoma or astrocytoma grade 4 Age 18-75 years Surgical treatment-resection. Scheduled concomitant radiochemotherapy, or only chemotherapy. Informed consent Exclusion Criteria: No informed consent Egg yolk allergy Only surgical biopsy Only radiotherapy

Sites / Locations

  • Skåne University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Salovum

Placebo

Arm Description

Salovum, an egg yolk powder will be orally at dose of 11 g 3 times daily.

Placebo, an egg yolk powder will be orally at dose of 11 g 3 times daily.

Outcomes

Primary Outcome Measures

Overall survival
Survival

Secondary Outcome Measures

Progress free survival at 6 and 12 months
Progress free survival as a compound assessment by a multidisciplinary conference (MDC)

Full Information

First Posted
December 20, 2022
Last Updated
June 20, 2023
Sponsor
Peter Siesjö
Collaborators
Lund University
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1. Study Identification

Unique Protocol Identification Number
NCT05669820
Brief Title
Antisecretory Factor Glioblastoma Phase 2
Acronym
AFGB2
Official Title
Antisecretory Factor During Concomitant and Adjuvant Therapy of Primary Glioblastoma, a Randomised, Prospective and Double Blinded Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 2023 (Anticipated)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
January 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Peter Siesjö
Collaborators
Lund University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
Antisecretory factor, Trials, Randomized Clinical

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomized, prospective, double blinded
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Eggyolk powder with same smell, texture and colour in identical packages.
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Salovum
Arm Type
Active Comparator
Arm Description
Salovum, an egg yolk powder will be orally at dose of 11 g 3 times daily.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, an egg yolk powder will be orally at dose of 11 g 3 times daily.
Intervention Type
Dietary Supplement
Intervention Name(s)
Salovum
Other Intervention Name(s)
Antisecretory factor
Intervention Description
Salovum is an eggyolkpowder derived from hens fed with SPC (specially processed cereals) and contains increased amounts of the endogenous protein antisecretory factor.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo egg yolk powder
Intervention Description
Egg yolk powder derived from hen fed with normal feed.
Primary Outcome Measure Information:
Title
Overall survival
Description
Survival
Time Frame
up to 12 months from primary surgery
Secondary Outcome Measure Information:
Title
Progress free survival at 6 and 12 months
Description
Progress free survival as a compound assessment by a multidisciplinary conference (MDC)
Time Frame
At 6 and 12 months from primary surgery
Other Pre-specified Outcome Measures:
Title
Cognitive function
Description
Assessed by Montreal Cognitive Assessment (MoCA)
Time Frame
up to 1 year
Title
Neurological function
Description
Assessed by Neurologic Assessment in Neuro-Oncology (NANO) scale
Time Frame
up to 1 year
Title
QOL Assessed by European Organization of Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C30
Description
Assessed by European Organization of Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C30 questionnaire
Time Frame
up to 1 years
Title
quality of life (QOL) assessed by brain cancer module (BN20) questionnaire
Description
Assessed by brain cancer module (BN20) questionnaire
Time Frame
up to 1 years
Title
Performance Assessed by Eastern Oncology Cooperative Group (ECOG) performance scale
Description
Assessed by Eastern Oncology Cooperative Group (ECOG) performance scale
Time Frame
up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pathology verified glioblastoma or astrocytoma grade 4 Age 18-75 years Surgical treatment-resection. Scheduled concomitant radiochemotherapy, or only chemotherapy. Informed consent Exclusion Criteria: No informed consent Egg yolk allergy Only surgical biopsy Only radiotherapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Siesjö, MD, PhD
Phone
+4646171274
Email
peter.siesjo@med.lu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Johan Bengzon, MD, PhD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charlotte Edwardsson
Organizational Affiliation
Skane University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Erik Ehinger, MD
Organizational Affiliation
Skane University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Skåne University Hospital
City
Lund
ZIP/Postal Code
22185
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter Siesjö, MD
Phone
+46705655778
Email
peter.siesjo@med.lu.se
First Name & Middle Initial & Last Name & Degree
Erik Ehinger, MD
Phone
+46707970783
Email
erik.ehinger@med.lu.se

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The datasets used and analysed in the current trial will be available in anonymized form after completion of the study, on reasonable request.

Learn more about this trial

Antisecretory Factor Glioblastoma Phase 2

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