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NCT Number: NCT05717699

Oncolytic Virus Ad-TD-nsIL12 for Progressive Pediatric Diffuse Intrinsic Pontine Glioma

This is a single-arm, single-center, drug safety assessment clinical trial with a 3+3 dose escalation design, to observe the safety, tolerability and toxicity of a novel oncolytic virus Ad-TD-nsIL12 intratumoral injection in progressive DIPG patients (NCI-CTCAE V5.0).

Recruiting

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent of the parents or patient.
  • After surgical resection, biopsy, chemotherapy, or radiation therapy, tumor progression must be confirmed by MRI scan.
  • Biopsy is performed prior to injection of Ad-TD-nsIL12 to confirm DIPG (frozen section-based).
  • Pre-enrollment patients LPS (patients aged ≥1 and <16 years) and KPS (patients aged ≥16 years) ≥ 50.
  • Patient must be, in the investigator opinion, able to comply with all the protocol procedures.
  • Age 1-18 years.
  • A negative pregnancy test in fertile women (women are considered of childbearing potential (WOCBP) after menarche, unless permanently infertile, including hysterectomy, bilateral salpingectomy, and bilateral oophorectomy).
  • Lesion considered by the investigator to be accessible for stereotactic biopsy.

Exclusion criteria

  • Serious infections or intercurrent conditions, including but not limited to severe renal failure, liver failure, heart failure, or bone marrow failure, which are not permitted for inclusion according to the investigator's criteria. Patients must be afebrile (<38℃) at the time of viral therapy.
  • Other investigational medications within 30 days prior to viral treatment.
  • Participants with immunodeficiency, autoimmune disease, or active hepatitis.
  • Any medical or psychological condition that might interfere with the patient's ability to participate if older than 16 years or parents ability when younger than 16, or give informed consent or would compromise the patient's ability to tolerate therapy or any disease that will obscure toxicity or dangerously alter drug metabolism.
  • Tumor with multiple location.
  • Pregnant or breast-feeding females.
  • Severe bone marrow hypoplasia.
  • Transaminases (aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT)) or total bilirubin > 3 times the upper limit of normal.
  • Neutrophils < 1x10^9/L.
  • Platelets ≤ 100x10^9/L.
  • Hemoglobin < 9g/dl.
  • Patients with Li-Fraumini syndrome or a known germline defect in the retinoblastoma gene or its associated pathways.
  • Administer any type of vaccine within 30 days prior to Ad-TD-nsIL12 administration.
  • Blood transfusions or drugs (such as G-CSF) within 28 days before viral treatment to treat pancytopenia or other hematological disorders.

Treatment and study plan

Ad-TD-nsIL12

Biological

After stereotactic biopsy, the Ommaya reservoir will be inserted through the biopsy channel and two injections of Ad-TD-nsIL12 will be delivered after surgery by Ommaya reservoir (with an interval of 3days). The interval between following injections in the subsequent treatment period will be 3 weeks ±4 days. The assigned dose for each patient will be 3x10^9vp, 1x10^10vp or 3x10^10 vp suspended in 1 ml NS according to cohort design.

Primary outcomes

  1. Safety of Ad-TD-nsIL12 intratumoral injection in progressive pediatric DIPG patients.

    Time frame: 3 months after virus injection

    The trial will look for possible hematologic and neurologic toxicity of Ad-TD-nsIL12 by NCI-CTCAE v5.0 to determine maximum tolerated dose of this oncolytic adenovirus.

Secondary outcomes

  1. Tumor response

    Time frame: 3 months after virus injection

    To determine tumor response by RAPNO criteria

  2. Over-all survival

    Time frame: 12 months after virus injection

    To determine overall survival at 12 months (OS12).

  3. QoL

    Time frame: 2 years after virus injection

    To measure quality of life baseline assessment and any changes over time by PedsQLTM criteria.

  4. Sample Collection

    Time frame: 3 months after virus injection

    Pre- and post- treatment tumor tissue will be collected and tested to determine the immune response of patients. Collected blood will be used to test possible hematotoxicity of Ad-TD-nsIL12.

Study contacts

Contact information is provided by the study sponsor or research team.

Xiao Qian, Dr.

CONTACT

[email protected]

18020295435

Sponsors and collaborators

Lead sponsor

Capital Medical University

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2028
First posted
Feb 8, 2023
Registry last updated
Feb 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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