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NCT05717712RecruitingPhase 1

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

Source: ClinicalTrials.gov · Last updated 28 Feb 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a 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 primary DIPG patients (NCI-CTCAE V5.0).

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
18 (estimated)
First submitted
18 Dec 2022
Start date
4 Jan 2023
Primary completion date
4 Jan 2025
Lead sponsor
Capital Medical University
NCT number
NCT05717712

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 18
  • From 4 Jan 2023 to the primary completion date, 4 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Other investigational medications within 30 days prior to viral treatment.
  • 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 baseline to treat pancytopenia or other blood disorders.

Other illness

  • 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 at baseline (\<38℃).
  • Participants with immunodeficiency, autoimmune disease, or active hepatitis.
  • Patients with Li-Fraumini syndrome or a known germline defect in the retinoblastoma gene or its associated pathways.

Lab values

  • 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 \< 9 g/dl.

Age

  • 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.

Other

  • Tumor with multiple location.
  • Pregnant or breast-feeding females.
  • Severe bone marrow hypoplasia.

Who the study is looking for

  • Informed consent of the parents or patient.
  • 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).
  • Patient newly diagnosed of DIPG in MRI.
  • Pre-enrollment patients LPS (patients aged ≥1 and \<16 years) and KPS (patients aged ≥16 years) ≥ 50.
  • Lesion considered by the investigator to be accessible for stereotactic biopsy. The location of the lesion allows injection without virus entering the ventricular system.
  • No previous treatment for DIPG.

Age in the registry: 1 year to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sanbo Brain Hospital, Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.