SBIR-STTR Award

IGF OT IGF I CLR as a NEO Adjuvant Treatment Option for Triple Negative Breast Cancer Period of Performance
Award last edited on: 6/17/22

Sponsored Program
SBIR
Awarding Agency
NIH : NIMHD
Total Award Amount
$1,999,370
Award Phase
1
Solicitation Topic Code
NCI
Principal Investigator
Andrew M May

Company Information

Cellectar Biosciences Inc (AKA: Novelos Therapeutics Inc~Novellas)

100 Campus Drive
Madison, NJ 07932
   (608) 441-8120
   slichaw@novelos.com
   www.cellectar.com
Location: Multiple
Congr. District: 11
County: Morris

Phase I

Contract Number: 261201500071C-3-0-0
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2015
Phase I Amount
$1,999,370
Poor prognosis of triple negative breast cancer (TNBC) is attributable to the absence of efficacious, molecularly-targeted, neoadjuvant therapies. Micrometastases contribute to poor prognosis by increasing recurrence rate. Consequently, an effective treatment option that is capable of targeting and sterilizing micrometastatic disease in patients with TNBC is warranted. I-125-CLR1404 is proposed as a neoadjuvant therapy option for TNBC patients. In the first aim of this proposal, I-125 will conjugated to a tumor-targeting moiety, CLR1404. Subsequently, the physico-chemical properties of I-125-CLR1404 will be characterized and the chemical reactions to maximize chemical yield and minimize the amount of chemical impurities will be optimized. I-125-CLR1404 will be synthesized reliably with a radiochemical yield > 60%, a radiochemical purity (final product) > 95%, and chemical purity (final product) >90.0%. In the second aim, I-125-CLR1404 will be characterized biologically in murine TNBC models. This will include the assessment of pharmacokinetics, radiation dosimetry, and the investigation of normal tissue toxicities. Hematological toxicity will most likely be dose-limiting. In the final aim, efficacy studies of I-125-CLR1404 in an appropriate murine model of TNBC will be conducted. It is hypothesize that neoadjuvant I-125-CLR1404 leads to reduced tumor metastasis and improved survival in clinically relevant mouse models of TNBC. Public Health Relevance Statement Data not available. NIH Spending Category Breast Cancer Cancer Clinical Research

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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