SBIR/STTR Research Award

IGF OT IGF RADIOIMMUNOTHERAPY OF MELANOMA WITH NOVEL LGG TO MELANIN

Award identifier 4db269cda9fb3abed85be5fd38062d681207e0e5319135218715796fac17e63eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$295,782

Program and phase

SBIR · Phase I

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Rad Immune Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
EZJ3T8AFYMC3
Solicitation number
Not reported
Topic code
NCI

Research abstract

In spite of several novel drugs for metastatic melanoma entering the market in the last few years there is an enormous need for novel effective treatments that would not rely on patients specific genotypes biochemical pathways or the variability of an individual s immune response Previously we conducted a successful Phase clinical trial of an antibody to melanin radiolabeled with beta emitter Rhenium However the IgM isotype of that antibody presented an impediment to further clinical development Recently we have identified a novel antibody to melanin with the IgG isotype which can be easily humanized for future clinical trials The long term goal of the proposal is to develop and bring to the market the radioimmunotherapy of metastatic melanoma based on this novel IgG to melanin We are planning the following Aims Perform the conjugation of C IgG with the chelating agents to enable radiolabeling with alpha and beta emitting therapeutic radionuclides Carry out pharmacokinetics pharmacodynamics studies of radiolabeled C in murine and human melanoma models Use the data from these studies to perform radiation dosimetry calculations Perform proof of concept RIT experiments in murine and human melanoma models Assess the efficacy and short term toxicity of the treatment We anticipate that both beta and alpha emitting radionuclide radiolabeled IgG to melanin will be effective in slowing down or abrogating experimental tumor growth and also safe towards all major organs Based on the realistic estimates of radionuclides commercial availability we will make the selection of the most suitable radiolabeled form of IgG to melanin for the future IND enabling experiments

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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