In this first-in human, phase I/IIa study, the safety and efficacy of \[212Pb\]VMT01, an alpha-particle emitting therapeutic agent targeted to melanocortin sub-type 1 receptor (MC1R) is being evaluated as a monotherapy and in combination with nivolumab in subjects with unresectable and metastatic melanoma.
This is a prospective, multi-center open-label dose-finding, dose-expansion study of \[212Pb\]VMT01 as a monotherapy or in combination with nivolumab in up to 300 subjects with histologically confirmed melanoma and a positive MC1R imaging scan with imaging agents \[203Pb\]VMT01 or \[68Ga\]VMT02. MC1R is a receptor that is expressed on the surface of melanoma cells and therefore is an attractive therapeutic target for melanoma treatment. Lead-212 (\[212Pb\]-) based peptide-radiopharmaceuticals are an emerging class of targeted alpha-particle cancer therapies that have potential to improve delivery of a highly effective form of radiation. This study will be conducted in 3 parts: Part 1: Monotherapy Dose-Finding Part 2: Combination-Therapy Dose-Finding Part 3: Dose Expansion Enrolled subjects in Monotherapy may receive up to 3 doses of \[212Pb\]VMT01 approximately 8 weeks apart and subjects in combination therapy may receive up to 3 doses of \[212Pb\]VMT01 along with nivolumab. Nivolumab will be administered every 4 weeks for up to 24 months. A Dosimetry sub-set utilizing an imaging surrogate, \[203Pb\]VMT01, has been incorporated into the study in order to assess organ biodistribution and tumor uptake of the investigational products. This study will also estimate radiation dosimetry and correlate uptake of the investigation products with observed toxicities and efficacy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
300
\[203Pb\]VMT01 is administered intravenous (IV) as an imaging agent for SPECT/CT
Subjects with positive uptake of \[203Pb\]VMT01 will receive a fixed dose of \[212Pb\]VMT01 administered IV every 8 weeks starting at Cycle 1 Day 1.
For all combination-therapy cohorts, 480 mg nivolumab will be administered every 4 weeks as an IV infusion.
University of California Irvine
Orange, California, United States
RECRUITINGUniversity of Miami
Miami, Florida, United States
RECRUITINGSarasota Memorial Hospital
Sarasota, Florida, United States
RECRUITINGUniversity of Iowa
Iowa City, Iowa, United States
RECRUITINGUniversity of Kentucky
Lexington, Kentucky, United States
RECRUITINGMayo Clinic Rochester
Rochester, Minnesota, United States
RECRUITINGSaint Louis University Hospital
St Louis, Missouri, United States
RECRUITINGWashington University of St. Louis
St Louis, Missouri, United States
RECRUITINGNebraska Cancer Specialists
Omaha, Nebraska, United States
RECRUITINGFox Chase Cancer Center
Philadelphia, Pennsylvania, United States
RECRUITING...and 2 more locations
Number of subjects with dose-limiting toxicities (DLTs) after the first administration of [212Pb]VMT01 as a monotherapy or in combination with nivolumab.
DLTs describe side effects of a drug that are serious enough to prevent an increase in dose
Time frame: Incidence of DLTs during the first 42 days of study Treatment will be assessed.
Objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1
Percentage of subjects with complete responses (CRs) or partial responses (PRs) to at least 1 administration of \[212Pb\]VMT01 as a monotherapy or in combination with nivolumab
Time frame: Up to approximately 2 years
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) following administration of [212Pb]VMT01 as a monotherapy or in combination with nivolumab
Any untoward medical occurrence in a clinical investigational participant administered \[212Pb\]VMT01 as a monotherapy or in combination with nivolumab. Associated AE or SAE is assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0
Time frame: Up to approximately 2 years
Duration of response (DOR) following treatment with [212Pb]VMT01 as a monotherapy and in combination with nivolumab as assessed by RECIST v1.1 criteria
DOR is time interval between the onset of a treatment response and the subsequent progression of disease or death
Time frame: Up to approximately 2 years
Progression free survival (PFS) for subjects receiving at least one administration of [212Pb]VMT01 as a monotherapy and in combination with nivolumab, as assessed by RECIST v1.1 criteria
PFS a measure of how long a patient with a cancer lives without their cancer progressing or worsening.
Time frame: Up to approximately 2 years
Determination of pharmacokinetic properties (PK) of [212Pb]VMT01: Area under the concentration versus time curve
Blood radioactivity PK endpoint reported as Ci\*h/L
Time frame: Up to week 16
Determination of pharmacokinetic properties of [212Pb]VMT01]: Apparent terminal elimination half-life (T1/2)
Blood radioactivity PK endpoint (reported as time in minutes)
Time frame: Up to week 16
ClinicalTrials at Perspectivetherapeutics
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