[203Pb]VMT-α-NET: \[203Pb\]VMT-α-NET is administered by intravenous bolus injection for single-photon emission computed tomography imaging.
[212Pb]VMT-α-NET: \[212Pb\]VMT-α-NET is administered by intravenous infusion for treatment of SSTR2 expressing tumors.
Study summary
This study is Phase I/IIa First-in-Human Study of \[212Pb\]VMT-α-NET Targeted Alpha-Particle Therapy for Advanced SSTR2 Positive Tumors
Eligibility
Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria:
1. Adult (ages ≥18) PRRT-naïve subjects with NETs or meningioma by local pathology.
2. Disease described clinically as: (a) Locally advanced/unresectable or metastatic NETs for dose-finding part of the study (b) Locally advanced/unresectable or metastatic GEP-NETs, bronchial NETs, pheochromocytoma, or paragangliomas for the dose-expansion part of the study (c) Requiring at least 1 prior surgery (resection/biopsy) and a maximum of 1 line of EBRT, if technically feasible, for meningioma.
3. For meningioma: histologically confirmed diagnosis of meningioma, i.e., all grades (1 to 3) per World Health Organization Classification of Tumors of the Central Nervous System (5th edition; WHO-CNS5)
4. Radiological evidence of measurable disease by: (a) For NETs: RECIST v1.1 criteria on CT with contrast or MRI of the areas of tumor involvement within 60 days of enrollment.
5. Lesions must have shown radiological evidence of disease progression in the 12 months prior to enrollment. (b) For meningioma: RANO meningioma criteria on contrast-enhanced skull MRI for meningioma within 3 weeks prior to enrollment.
6. Demonstration of lesional SSTR expression: (a) For NETs: using an FDA-approved somatostatin receptor PET imaging agent, e.g. \[68Ga\]DOTATATE, \[64Cu\]DOTATATE, or \[68Ga\]DOTATOC (b) For meningioma: using a standard-of-care SSTR PET imaging agent within 45 days of enrollment
7. ECOG Performance Status ≤ 1.
8. Subjects with HIV positivity are allowed if CD4 Count \> 350 cells/μL.
9. Concurrent Somatostatin Analog (SSA) Therapy use while on protocol therapy is allowed provided that the subject must be able to tolerate withholding long-acting SSA therapy for a minimum of 28 days and short-acting SSA therapy for a minimum of 24 hours before the first and subsequent administrations of \[203Pb\]VMT-α-NET or \[212Pb\]VMT-α-NET
10. For NETs: Progressive Disease on approved therapies other than radionuclide therapy.
11. For subjects with meningioma who are receiving corticosteroid treatment, the dose must be ≤ 4 mg/day dexamethasone (or other corticosteroid equivalent dose) for a minimum of 7 days before the initiation of study treatment.
12. Must have clinically demonstrated adequate catecholamine blockade if catecholamine-secreting pheochromocytoma/paraganglioma tumors are present.
13. Able to understand and sign informed consent and comply with all study requirements.
14. Life expectancy \> 3 months.
15. Satisfactory organ function as determined by laboratory testing.
16. For females of reproductive potential: agree to use of highly effective contraception and refrain from donating eggs (ova, oocytes) for the purpose of reproduction starting from screening, during treatment, and for at least 6 months after the last dose of \[212Pb\]VMT-α-NET
17. For males of reproductive potential: agree to use of condoms or other methods to ensure effective contraception with partner and refrain from donating sperm starting from screening, during treatment, and for at least 6 months after the last dose of \[212Pb\]VMT-α-NET
Exclusion Criteria:
1. Known hypersensitivity to SSA, SSTR imaging agents or any of the excipients of \[212Pb\]VMT-α-NET.
2. Known additional malignancy that is progressing or requires active treatment.
3. Pregnancy or breastfeeding a child.
4. Febrile illness within 48 hours of any scheduled \[212Pb\]VMT-α-NET administration should be rescheduled \> 48 hours after resolution of fever\].
5. Treatment with another investigational medicinal product within 30 days of anticipated treatment.
6. Prior treatment with systemic PRRT based therapies (i.e., \[90Y\] DOTATATE/DOTATOC or \[177Lu\] DOTATATE)
7. Prior treatment with 90-Yttrium radioembolization must be completed at least 6 months prior to enrollment.
8. External beam radiation therapy (EBRT) must be completed at least 30 days prior to enrollment.
9. Subjects who have received prior treatment with 90Y radioembolization or EBRT should have radiation absorbed dose to critical organs documented.
10. Prior treatment with systemic anticancer therapy must be completed at least 30 days prior to enrollment (except for SSAs in subjects with functional tumors).
11. Major surgery must be completed at least 30 days prior to enrollment.
12. For Subjects with NETs: Known brain metastases; unless these metastases have been treated and stabilized 6 months prior to enrollment and the subject has been off steroid support for at least 14 days prior to enrollment.
13. Recently diagnosed and active infections requiring a time-limited course of antifungals or antibiotics in the 3 days prior to enrollment.
14. Receipt of live attenuated vaccines in the 7 days prior to enrollment.
15. Grade 3 nausea/vomiting or diarrhea within 72 hours before the of first scheduled dose of \[212Pb\]VMT-α-NET despite adequate antiemetic and other supportive care
16. Known medical condition which would make this protocol unreasonably hazardous for the subject.
17. Medical history of a condition resulting in a severe allergic reaction such as anaphylaxis or angioedema to known components of the Investigational Medicinal Product or excipients.
18. Current abuse of alcohol or illicit drugs (exclusive of use of medically prescribed cannabinoids).
19. Existence of any medical or social issues likely to interfere with study conduct or that may cause increased risk to the subject or to others, e.g., lack of ability to follow radiation safety precautions.
20. QTc \> 450 milliseconds for males and females.
Primary outcome measure(s)
Number of participants with dose-limiting toxicities (DLTs) after the first administration of [212Pb]VMT-α-NET — Incidence and severity of DLTs during the first 42 days of study treatment will be assessed. DLTs describe side effects of a drug that are serious enough to prevent an increase in dose
Objective response rate (ORR) per Response Evaluation Criteria in Solid Tumours (RECIST) Version 1.1 in subjects with NETs — Up to week 96 Percentage of subjects with complete responses (CRs) or partial responses (PRs) to at least 1 administration of \[212Pb\]VMT-α-NET
ORR per Response Assessment in Neuro-Oncology (RANO) meningioma criteria in subjects with meningioma — Up to week 96 Percentage of subjects with complete responses (CRs) or partial responses (PRs) to at least 1 administration of \[212Pb\]VMT-α-NET
Number of subjects with adverse events (AEs) — Until the end of study (3 years after end-of-study visit) Any untoward medical occurrence in a clinical investigational participant administered \[212Pb\]VMT-α-NET and which does not necessarily have a causal relationship with this treatment. Associated Adverse Events (AE) or Serious AEs are assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Trial sites (19)
Facility
City
Region
Status
Mayo Clinic
Jacksonville
Florida
Recruiting
Biogenix Molecular
Miami
Florida
Recruiting
The University of Chicago
Chicago
Illinois
Recruiting
University of Iowa
Iowa City
Iowa
Recruiting
University of Kentucky
Lexington
Kentucky
Recruiting
Johns Hopkins
Baltimore
Maryland
Recruiting
Barbara Ann Karmanos Cancer Institute
Detroit
Michigan
Recruiting
BAMF Health
Grand Rapids
Michigan
Recruiting
Michigan Health Professionals
Troy
Michigan
Recruiting
Mayo Clinic
Rochester
Minnesota
Recruiting
Washington University
St Louis
Missouri
Recruiting
Nebraska Cancer Specialists
Omaha
Nebraska
Recruiting
University of North Carolina
Chapel Hill
North Carolina
Recruiting
UH Cleveland Medical Center
Cleveland
Ohio
Recruiting
Ohio State University
Columbus
Ohio
Recruiting
Vanderbilt-Ingram Cancer Center
Nashville
Tennessee
Recruiting
Virginia Cancer Specialists
Fairfax
Virginia
Recruiting
Fred Hutchinson Cancer Center
Seattle
Washington
Recruiting
Froedtert Medical College of Wisconsin
Milwaukee
Wisconsin
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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