NCT07767110Not yet recruitingPhase 1/2
Targeted LSAM-Cisplatin Infusion in Gliomas, Evaluation of Response
Phase 1/2a Study to Determine the Safety of Intratumoral Infusion of Large Surface Area Microparticle (LSAM)-Cisplatin in Participants With Diffuse Midline Glioma (DMG), Including Diffuse Intrinsic Pontine Glioma (DIPG)
Source: ClinicalTrials.gov · Last updated 18 Aug 2026
Brief summary (registry, in English)
Open-label, dose-escalating, Phase 1/2a trial of Large Surface Area Microparticle (LSAM)-Cisplatin to treat participants with diffuse midline glioma (DMG), including diffuse intrinsic pontine glioma (DIPG), via stereotactic infusion under intraoperative magnetic resonance imaging (MRI) guidance.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 1/2
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 11 Aug 2026
- Start date
- 1 Dec 2026
- Primary completion date
- 31 Dec 2029
- Lead sponsor
- NanOlogy, LLC
- Diseases
- Childhood cancers
- NCT number
- NCT07767110
What you commit to
- Study type: Interventional · Phase 1/2
- Planned participants: 20
- From 1 Dec 2026 to the primary completion date, 31 Dec 2029
- No sites listed in no 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
- Receiving any anticoagulants or antiplatelet drugs; any drugs known to cause ototoxicity and nephrotoxicity; receiving any other tumor-directed therapy.
Other illness
- Untreated symptomatic hydrocephalus at the time of consent, has metastatic or disseminated disease, or leptomeningeal disease.
- Known allergy or hypersensitivity to the study agent (including cisplatin and diluent components).
Lab values
- Intercurrent illnesses or conditions which preclude participation: active systemic infections, autoimmune disease requiring systemic immunomodulation, active or uncontrolled seizure disorder, central nervous system (CNS) vasculopathy or aneurysms, Grade ≥3 cardiac dysfunction, Fridericia-corrected QT interval (QTcF) ≥470 ms.
- Abnormal organ function:
- Renal insufficiency: glomerular filtration rate (GFR) ≤ 60 mL/min/1.73m² (with Schwartz equation)
- Hepatic dysfunction: aspartate aminotransferase (AST) / alanine aminotransferase (ALT) ≤ 1.5 x upper limit of normal (ULN) and 3 x upper limit of normal (ULN) in the presence of liver metastases; or bilirubin ≤ 1.5 x upper limit of normal (ULN) and 3 x upper limit of normal (ULN) in the presence of Gilbert disease
- Bone marrow suppression:
- absolute neutrophil count (ANC) \< 1,000/μL
- platelets \< 100,000/μL
- Coagulopathy or international normalized ratio (INR) \> 1.5
Other
- Magnetic resonance imaging (MRI) findings that preclude stereotactic procedure.
- Female participants of childbearing potential must not be pregnant or breast-feeding.
Who the study is looking for
- Aged 3 to ≤ 21 years.
- Diagnosis of diffuse midline glioma (DMG), including diffuse intrinsic pontine glioma (DIPG), based on characteristic magnetic resonance imaging (MRI) findings and/or histopathologic confirmation.
- Prior radiation treatment must have included focal radiation therapy per institutional standard of care and must have been initiated within 6 weeks of diagnosis.
- At least 4 weeks, but no more than 12 weeks, post-completion of radiotherapy treatment.
- A standard of care post-radiation magnetic resonance imaging (MRI) performed 4 to 6 weeks after radiation therapy is required for confirmation of eligibility.
- Performance status \[Karnofsky Performance Scale or Lansky Performance Score\] within 14 days of Day 1 ≥ 60.
- Absence of other significant medical condition.
- A legal parent/guardian and/or participant must be able to understand and be willing to sign a written informed consent and/or assent document, as appropriate.
Age in the registry: 3 years to 21 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.