MPNST (Malignant Peripheral Nerve Sheath Tumor)

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Review clinical trials related to MPNST (Malignant Peripheral Nerve Sheath Tumor). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Combination of Avutometinib and Defactinib for Treatment of Relapsed, Refractory, Metastatic, or Unresectable Malignant Peripheral Nerve Sheath Tumor

The purpose of this study is to learn whether the study drugs avutometinib and defactinib can help stop or shrink malignant peripheral nerve sheath tumors (MPNST) that have returned or cannot be removed with surgery.

Participants needed: 23
Trial details
Phase: Phase 2Age: 12+Biological sex: AllType: InterventionalSponsor: Girish Dhall, MDUpdated: Aug 4, 2026
Eligibility criteria

Age > 12 years old with a body surface area (BSA) of at least 1.5 mm2 [+33]

Current warfarin use. If a participant is currently being treated for a pulmonar... [+14]

Status: Available

BLESSED: Expanded Access for DNG64-CAR-V for Advanced Pancreatic Cancer, Sarcoma and Carcinoma of Breast

Forty patients with pancreatic cancer, sarcoma and carcinoma of breast will receive DNG64-CAR-V intravenously or intratumorally at a dose of 1-4 x 10e11 colony forming units (cfu) or equivalent 1.0-6.0 x 10e10 Vector Copies (VC) per dose one to three times a week. DNG64-CAR-V may be given alone or with one or more FDA approved cancer therapies/immunotherapies, or with certain FDA authorized investigational agents. Based on previous Phase 1/2 US based clinical studies, DNG64-CAR-V does not suppress the bone marrow or cause organ dysfunction, and enhanced immune cell trafficking in tumors may cause the tumors to appear larger or new lesions to appear on CT, PET or MRI (pseudoprogression). Further, tumor stabilization/regression/remission have occurred later during the treatment period with DNG64-CAR-V monotherapy. Therefore, DNG64 -CAR-V will be continued if the patient has clinical benefit and does not have symptomatic disease progression.

Trial details
Age: 12-100Biological sex: AllType: Expanded AccessSponsor: Aveni FoundationUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Patient is ≥12 years of age, either male or female for patients with sarcoma; >1... [+4]

Patient is unwilling to provide formal informed consent. [+1]