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Virus Therapy

EO4010 for Colorectal Cancer (AUDREY Trial)

Phase 1 & 2
Waitlist Available
Research Sponsored by Enterome
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12months
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a new drug on participants at multiple locations with no placebo or blinds.

Who is the study for?
This trial is for adults over 18 with advanced, non-resectable colorectal adenocarcinoma that's HLA-A2 positive. They must have had prior treatment or be unsuitable for standard therapies, have a life expectancy of at least 3 months, and agree to contraception. Exclusions include recent high-dose steroids or chemotherapy, unresolved toxicities, certain abnormal lab values (like low blood counts), active infections including TB/HIV/HBV/HCV, pregnancy/breastfeeding, history of severe allergies to study drug components or autoimmune disorders.
What is being tested?
EO4010 is being tested in this open-label multicenter study on patients with metastatic colorectal cancer who've already undergone treatment. The focus is on the safety and effectiveness of EO4010 as a potential new therapy option.
What are the potential side effects?
While specific side effects for EO4010 are not listed here, common side effects from similar cancer treatments may include fatigue, nausea, diarrhea, lowered immunity leading to increased infection risk; allergic reactions; and potentially organ-specific inflammation.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Safety and tolerability of EO4010 in combination with nivolumab and/or bevacizumab
Secondary study objectives
Disease control rate
Duration of response
Overall response rate
+4 more

Side effects data

From 2024 Phase 3 trial • 529 Patients • NCT02017717
80%
Fatigue
70%
Diarrhoea
70%
Headache
40%
Vomiting
40%
Aspartate aminotransferase increased
40%
Rash maculo-papular
40%
Alanine aminotransferase increased
40%
Lipase increased
30%
Partial seizures
30%
Hemiparesis
30%
Gait disturbance
30%
Fall
30%
Cough
30%
Dry skin
30%
Amylase increased
30%
Nausea
30%
Confusional state
20%
Malignant neoplasm progression
20%
Pyrexia
20%
Candida infection
20%
Mucosal infection
20%
Decreased appetite
20%
Back pain
20%
Dysphonia
20%
Hypotension
20%
Colitis
20%
Hyperthyroidism
20%
Oedema peripheral
20%
Muscular weakness
20%
Hypothyroidism
10%
Tinnitus
10%
Cushingoid
10%
Diabetic ketoacidosis
10%
Procedural haemorrhage
10%
Blood bilirubin increased
10%
Bradycardia
10%
Sinus tachycardia
10%
Hyperglycaemia
10%
Hypocalcaemia
10%
Neck pain
10%
Brain oedema
10%
Hydrocephalus
10%
Lethargy
10%
Seizure
10%
Hypertension
10%
Palpitations
10%
Cheilitis
10%
Presyncope
10%
Face oedema
10%
Oedema
10%
Conjunctivitis
10%
Enterocolitis infectious
10%
Oral candidiasis
10%
Pneumonia
10%
Sinusitis
10%
Staphylococcal infection
10%
Blood alkaline phosphatase increased
10%
Spinal pain
10%
Tremor
10%
Dizziness
10%
Dysarthria
10%
Urinary retention
10%
Dyspnoea exertional
10%
Nasal congestion
10%
Pneumonitis
10%
Dermatitis
10%
Erythema
10%
Rash
10%
Klebsiella infection
10%
Hypomagnesaemia
10%
Syncope
10%
Haemorrhage intracranial
10%
Pancreatitis
10%
Cholecystitis
10%
Upper respiratory tract infection
10%
Acute kidney injury
10%
Dermatitis bullous
10%
Lymphopenia
10%
Optic nerve disorder
10%
Visual impairment
10%
Dehydration
10%
Hypokalaemia
10%
Scoliosis
10%
Cognitive disorder
10%
Memory impairment
10%
Hallucination
10%
Insomnia
10%
Irritability
10%
Urinary incontinence
10%
Dyspnoea
10%
Dermatitis acneiform
10%
Pelvic venous thrombosis
10%
Sepsis
100%
80%
60%
40%
20%
0%
Study treatment Arm
Cohort 1: Arm N1+I3
Cohort 2: Arm B
Part A Cohort 1c: Arm N3+RT+TMZ
Part A Cohort 1d: Arm N3+RT
Part B Cohort 1c: Arm N3+RT+TMZ
Part B Cohort 1d: Arm N3+RT
Cohort 1: Arm N3
Cohort 1b: Arm N3+I1
Cohort 2: Arm N3

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Cohort 3Experimental Treatment1 Intervention
E04010 in combination with nivolumab and/or bevacizumab
Group II: Cohort 2Experimental Treatment1 Intervention
E04010 in combination with nivolumab
Group III: Cohort 1Experimental Treatment1 Intervention
E04010 Monotherapy

Find a Location

Who is running the clinical trial?

EnteromeLead Sponsor
8 Previous Clinical Trials
511 Total Patients Enrolled
Jan FagerbergStudy DirectorEnterome
1 Previous Clinical Trials
70 Total Patients Enrolled
~18 spots leftby Feb 2026
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