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Taking people in SwedenPhase 2/3

Tests an egg powder with antisecretory factor in newly diagnosed glioblastoma

Compares an egg powder enriched with antisecretory factor against placebo in adults with glioblastoma.

Plain-language title generated from the registry record
Registry title: Antisecretory Factor Glioblastoma Phase 2

Key facts

Where
Lund, SwedenSee the site
Phase
Phase 2/3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT05669820, who can take part

Where in Sweden

  • Skåne University HospitalLund, SwedenTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Peter Siesjö
Trial code
NCT05669820
Record updated
9 January 2026
Original description
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 diagnosisRead full original descriptionShow less

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

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

Inclusion: Pathology verified glioblastoma or astrocytoma grade 4; Age 18-75 years; Surgical treatment-resection; Scheduled concomitant radiochemotherapy, or only chemotherapy; Informed consent.

Exclusion: Only surgical biopsy; Only radiotherapy; Egg yolk allergy; No informed consent.

ClinicalTrials.gov NCT05669820