Antisecretory Factor for Newly Diagnosed Glioblastoma
Antisecretory Factor Glioblastoma Phase 2
Recruiting
Phase 2Phase 3Interventional Study
Glioblastoma
Pivotal Trial
This treatment is in the last trial phase before FDA approval.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 2/3
Study type
Interventional
Purpose
Treatment
Participants needed
300 (estimated)
Sponsor
Peter Siesjö · Other
Who this trial is looking for
This trial is looking for adults with newly diagnosed glioblastoma. Participants will take either an egg powder containing a special factor or a placebo daily around the time they receive chemotherapy and radiotherapy.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with glioblastoma or grade 4 astrocytoma.
I am between 18 and 75 years old.
I have had surgical treatment for my tumor.
I am scheduled to receive radiochemotherapy or chemotherapy.
I can provide informed consent.
You may not be able to join if
I cannot provide informed consent.
I am allergic to egg yolk.
I have only had a surgical biopsy.
I will only receive radiotherapy.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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 ove…
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
Trial Locations
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Eligibility Criteria
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 b…
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
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