About this trial

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.

Eligibility criteria

Qualifiers

Ability to understand and willingness to provide informed consent, willingness to comply with all study procedures for the duration of the study

Aged ≥ 18 years

Diagnosed with unresectable Stage III or Stage IV metastatic or recurrent melanoma

Previously progressed (radiological progression) on at least one approved systemic therapy for advanced melanoma

Disqualifiers

Active secondary malignancy

Prior systematic treatment with radioactive nuclides. Subjects who had localized treatment with radioactive nuclides or imaging using radioactive imaging agents may be enrolled

Pregnancy or breastfeeding a child

Any serious/active/uncontrolled infection requiring parenteral antibiotics within 2 weeks before the first administration of [212Pb]VMT01

Trial design

Treatments tested in this trial

  • [203Pb]VMT01
  • [212Pb]VMT01
  • Nivolumab

Treatment groups

300 Participants
are divided into 4 treatment groups

Locations

13
California
University of California Irvine92868, Orange United States
Florida
Mayo Clinic32224, Jacksonville United States
University of Miami33136, Miami United States
Sarasota Memorial Hospital34239, Sarasota United States

Sponsors and collaborators

Perspective Therapeutics

Lead sponsor