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Evaluation of Neuroblastoma cancer treatment by optimized measles vaccine

The first phase and second of the trial investigating the safety and efficacy of Intratumorally optimized measles vaccine in patients with Neuroblastoma cancer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230903059342N4
Enrollment
10
Registered
2025-11-11
Start date
2025-11-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Neuroblastoma Cancer. Malignant neoplasm of peripheral nerves and autonomic nervous system

Interventions

Intervention 1: Intervention group: includes patients who, in addition to standard treatment, receive the optimized measles vaccine intraperitoneally in 2 doses 4 weeks apart. At the same time as bei

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 21 Years

Inclusion criteria

Inclusion criteria: Patient age 2 to 21 The patient must be considered by a pediatric oncologist to be refractory to conventional treatments or for which there is no standard treatment. The non-central nervous system solid tumor has been confirmed by a histologist. Proper functioning of liver, kidney and bone marrow The ability to understand and sign the consent form by the patient and one of these cases: the patient's spouse, parent or guardian. Complying with all protocol steps including sample submission and returning to the clinical study site for subsequent visits Absence of autoimmune diseases or diseases of the immune system

Exclusion criteria

Exclusion criteria: Life-threatening acute infection Absence of any previous record that describes the doctor's treatment and orders were nor followed by patient. Using drugs that weaken the immune system Affected by any diseases that disturbs the immune system Having any previous record of organ transplantation Allergy to measles vaccine Using other investigational treatments at the same time

Design outcomes

Primary

MeasureTime frame
Fever. Timepoint: Hourly in the first 24 hours and then daily up to 7 days. Method of measurement: Thermometer.;Examining changes in the patient's heart condition. Timepoint: Hourly after the start of treatment for up to 7 days. Method of measurement: Electrocardiogram.;Examining changes in the patient's breathing status. Timepoint: Hourly in the first 24 hours and then daily up to 7 days. Method of measurement: pulse oximeter.;Examination of tumor size. Timepoint: Weekly until 6 months after the end of treatment. Method of measurement: Sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRuhollah Dorostkar

Bagheiat-allah University of Medical Sciences

R.dorost@yahoo.com+98 21 8817 0179

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026