Clinical Trial Finder

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  INCLUSION CRITERIA:

  - Participants must have histopathologically confirmed gastrointestinal neuroendocrine tumors (GI NET), pheochromocytoma/paraganglioma (PPGL), small cell lung cancers (SCLC), kidney cancers (KC), or Head & Neck cancers (nasopharyngeal carcinoma [NPC], olfactory neuroblastoma [ONB], sinonasal neuroendocrine carcinoma [SNEC]) that are metastatic or inoperable per Standard of Care.

Note: for KC, all histopathologies of kidney cancers are eligible as long as it is a primary renal neoplasm.

• - Required prior therapies: - GI NET, PPGL, H&N: no specific prior therapy is needed.

• - SCLC: At least one prior line of standard of care systemic treatment such as chemotherapy and/or immunotherapy.

• - KC: Renal cell carcinoma (RCC) participants should have received at least one line of prior therapy in the metastatic setting and should have received at least one Programmed cell death protein 1 (PD1) / Programmed death-ligand 1 (PDL1)-targeted immune checkpoint inhibitor as well as one agent targeting the VEGF pathway.

Participants with fumarate hydratase (FH) deficient RCC should have received at least one prior line of systemic therapy (such as bevacizumab plus erlotinib). No prior therapy is needed for participants with other histologic subtypes.

• - Have NOT received prior systemic radioligand therapy for definitive therapeutic purposes.

Prior external beam radiation therapy is allowed.

• - History of disease progression by imaging (e.g., RECIST 1.1) or clinically (defined as increase in severity or frequency of symptoms related to disease) within the past 36 months prior to the first dose of [203Pb]VMT-Alpha-NET.

• - Evidence of somatostatin receptors (SSTR) expression on at least 50% of the radiographically identifiable (i.e., visible on an anatomic scan such as CT or magnetic resonance imaging [MRI]) tumor, as indicated by a positive (uptake qualitatively identifiable as above the local background) on SSTR PET scan.

• - Age >= 18 years.

• - ECOG performance status <=1.

• - Participants must have adequate organ and marrow function as defined below: - Leukocytes: 3,000/microliter.

• - Absolute Neutrophil Count: 1,500/microliter.

• - Platelets 100,000/microliter.

• - Hemoglobin >= 9.0 g/dL.

• - Total bilirubin: within normal institutional limits.

Note: <= 5 X institutional upper limit of normal (ULN) if bilirubin elevation is due to a benign process such as Gilbert syndrome.

• - AST: <= 2.5 X institutional ULN.

• - ALT: <= 2.5 X institutional ULN.

• - Creatinine: within normal institutional limits.

OR.

• - Calculated creatinine clearance (glomerular filtration rate (eGFR): >= 60 mL/min/1.73 m^2 for participants with creatinine levels above institutional normal.

• - Participants with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression at screening.

• - Participants with new or progressive brain metastases or leptomeningeal disease are eligible as long as the participant is asymptomatic and not requiring medication for symptom control from the brain lesions at screening.

• - Participants seropositive for human immunodeficiency virus (HIV) must: - be on effective anti-retroviral therapy; and.

• - have an undetectable viral load at screening.

• - Participants seropositive for hepatitis B virus (HBV), must have HBV viral load undetectable at screening.

• - Participants seropositive for hepatitis C virus (HCV) must: - received curative treatment; and.

• - have an undetectable HCV viral load at screening.

• - Individuals of child-bearing potential (IOCBP) and individuals who can father children must agree to use an effective method of contraception (barrier, hormonal, intrauterine device [IUD], surgical sterilization, abstinence) at study entry and up to 6 months after the last dose of the study agent(s).

• - Nursing participants must be willing to discontinue nursing from study treatment initiation through 6 months after the last dose of the study agents.

• - The ability of the participant to understand and the willingness to sign a written informed consent document.

EXCLUSION CRITERIA:

• - Any investigational agents should be stopped at least 28 days prior to the first dose of [203Pb]VMT-Alpha-NET.

• - Systemic therapy should be stopped at least 28 days prior to the first dose of [203Pb]VMT-Alpha-NET (participants with prior systemic therapies for their malignancy only, except participants with SCLC).

• - Systemic therapy should be stopped at least 14 days prior to the first dose of [203Pb]VMT-Alpha-NET (participants with SCLC only).

• - History of allergic reactions attributed to compounds of similar chemical or biologic composition to VMT-Alpha-NET.

• - Positive Beta human chorionic gonadotropin (Beta-HCG) serum or urine pregnancy test performed in IOCBP at screening.

• - QTc > 450 ms on electrocardiogram (EKG) at screening.

Note: Framingham correction for QTc will be used.

• - History of or detection at screening of active/untreated secondary malignancy except nonmelanoma skin cancer and carcinoma in situ of the uterine cervix.

• - Uncontrolled intercurrent illness, factors, evaluated by medical history and physical exam which would potentially increase in the risk of the participant.

Background:

• - Somatostatin receptors (SSTR) have been shown to be over-expressed in a number of human tumors, including gastrointestinal (GI) neuroendocrine tumors (NET), pheochromocytoma/paragangliomas (PPGL), small cell lung cancers (SCLC), kidney cancers (KC), and some head and neck (H&N) cancers.

• - Targeted radioligand therapy (TRT) is a class of cancer therapeutic agents formed by attaching a radioactive isotope to a ligand that can target specific surface receptors such as SSTR on a tumor cell membrane.

Efficacy is typically determined by the radiation dose deposited onto a tumor, which is determined by the radioactive isotope being used as well as the binding characteristics of the ligand-receptor/transporter pair.

• - Alpha emitters such as 212Pb emit alpha particles that are more damaging to tumor cells than beta emitters such as 177Lu.

Therefore, TRT agents using alpha emitters are considered to be more potent than beta-emitting TRTs.

• - VMT-Alpha-NET is a peptide that binds to SSTR, which when attached to 212Pb becomes an alpha particle-emitting TRT that can be used to treat tumors that have SSTR surface expression.

• - [203Pb]VMT-Alpha-NET is the chemically identical imaging surrogate for [212Pb]VMT-Alpha-NET and has the same mechanism of action via binding to SSTR2.

The nuclide 203Pb contained in [203Pb]VMT-Alpha-NET emits gamma radiation suitable for single-photon emission computerized tomography (SPECT) imaging. These images can be used to assess drug product biodistribution throughout the body. Objective: -To determine the maximum tolerated dose (MTD) of [212Pb]VMT-Alpha-NET (dose escalation cohort) and assess the safety of [212Pb]VMT-Alpha-NET at the MTD (dose expansions cohorts). Eligibility:

• - Age >= 18 years.

• - Histopathologically confirmed GI NET, PPGL, SCLC, KC, or H&N (nasopharyngeal carcinoma [NPC], olfactory neuroblastoma [ONB], sinonasal neuroendocrine carcinoma [SNEC]) cancers that are metastatic or inoperable.

• - No prior systemic radioligand therapy.

• - Eastern Cooperative Oncology Group (ECOG) Performance Status <= 1.

Design:

• - This is an open-label, single-arm, single-center, phase I study evaluating the safety, preliminary efficacy, and pharmacokinetic properties of [212Pb]VMT-Alpha-NET in GI NET, PPGL, SCLC, KC, or H&N cancers.

• - First, participants will be accrued in Dose Escalation Part with 4 dose levels to estimate MTD of [212Pb]VMT-Alpha-NET.

Once MTD is estimated, the following participants with GI NET, PPGL, SCLC, KC, or H&N cancers will be accrued in separate cohorts and treated at MTD of [212Pb]VMT-Alpha-NET.

• - [212Pb]VMT-Alpha-NET will be given IV every 8 weeks for a total of 4 administrations.

• - A subset of participants (Dosimetry Arm 1) will have [203Pb]VMT-Alpha-NET administration followed by whole-body gamma scans combined with dosimetry SPECT/ Computed Tomography (CT) scans and collection of blood and urine samples prior to the first and the second doses of [212Pb]VMT-Alpha-NET (Cycles 1-2).

• - All participants will undergo serial whole-body dose rate measurements after [203Pb]VMT-Alpha-NET and/or [212Pb]VMT-Alpha-NET administration.

• - Participants will have timed clinical laboratory evaluations, imaging studies, and research blood, and urine samples while on the study therapy for safety and efficacy evaluations.

• - Following completion of treatment, participants will be seen at the NIH Clinical Center approximately 30 days later, every 12 weeks for 3 years after that for safety and efficacy assessments.

Beyond 3 years, participants will be contacted annually through any NIH-approved platform to assess for overall survival and health status.

Arms

Experimental: 1/Dosimetry Arm 1

Escalating doses of [212Pb]VMT-alpha-NET, imaging with [203Pb]VMT-alpha-NET

Experimental: 2/Arm 2

Escalating doses of [212Pb]VMT-alpha-NET

Experimental: 3/Arm 3

[212Pb]VMT-alpha-NET at MTD

Interventions

Drug: - 68Ga-DOTATATE

68Ga-DOTATATE PET/CT whole-body scanning will be done at at different intervals to monitor disease.

Drug: - [203Pb]VMT-alpha-NET

[203Pb]VMT-alpha-NET will be given IV 7 days prior to [212Pb]VMT-alpha-NET.

Drug: - [212Pb]VMT-alpha-NET

[212Pb]VMT-alpha-NET will be given IV on Day 1 of every cycle for 4 cycles total at escalating doses in Phase I and at MTD during dose expansion. One cycle is 8 weeks.