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FBO DAILY ISSUE OF MAY 26, 2010 FBO #3105
SOLICITATION NOTICE

A -- Large Animal Studies for Nanotherapeutics

Notice Date
5/24/2010
 
Notice Type
Combined Synopsis/Solicitation
 
NAICS
541711 — Research and Development in Biotechnology
 
Contracting Office
Department of Health and Human Services, National Institutes of Health, National Cancer Institute, Bldg 427, Room 12, Frederick, Maryland, 21702
 
ZIP Code
21702
 
Solicitation Number
S10-155
 
Archive Date
7/14/2010
 
Point of Contact
Matt DeSantis, Phone: 301/228-4002, Shannon B Jackson, Phone: 301-228-4022
 
E-Mail Address
desantisma@mail.nih.gov, jacksonshannon@mail.nih.gov
(desantisma@mail.nih.gov, jacksonshannon@mail.nih.gov)
 
Small Business Set-Aside
N/A
 
Description
ALL INTERESTED OFFERORS ARE TO CONTACT MATT DESANTIS AT DESANTISMA@MAIL.NIH.GOV AND REQUEST THE APPROPRIATE RFP TYPE FOR THEIR ORGANIZATION: TIME & MATERIALS OR COST REIMBURSEMENT. The National Cancer Institute (NCI), part of the National Institutes of Health, has established the NCI Alliance for Nanotechnology in Cancer (http://nano.cancer.gov) to harness the power of nanotechnology to reduce the burden of cancer. Several, recent developments have demonstrated that improved approaches to therapy can be realized using nanotechnology. The development of new therapies based on localized nanoparticle delivery is of particular interest to oncology due to the potential for delivery of lower doses of the drug or drug candidates with equal or improved efficacy and lowered side effects. There is a pressing need to enable the testing of nanoscale devices, delivery systems and drug payloads using appropriate animal models for preclinical safety and efficacy testing in GLP certified contract research organizations (CROs), academic institutions or pharmaceutical facilities. Prior to initial entry of a new drug or biologic agent into humans, the basis for the determination of in vivo safety is the preclinical testing performed in animals. Traditional drug development programs evaluating the safety of small molecule or protein therapeutics, typically conduct toxicology testing in normal animals using a well-defined paradigm to establish the acute, subchronic, and cumulative toxicities of an agent prior to its first exposure in large animals and eventually in humans. The advantages of this approach include: • testing a wide range of doses • investigating multiples of the expected human exposure; • Evaluating the mechanism of action and efficiency of binding of the device/therapeutic payload with the desired target • understanding the metabolism and disposition profiles in a different species • establish a basis for comparison for clinical dosing and the background incidence of any specific, adverse finding • provide well-documented efficacy data in the particular strain of animals being tested (deployed as the first of two animal species that need to be used for the initial demonstration of safety) Note: for the purposes of filing IND (Investigational New Drug) application with FDA, typically testing in both rodents (i.e. mice, rats, or hamsters), and one non-rodent species (e.g. dog, pig, or non-human primate) is required. The use of more than one species in traditional drug evaluation programs is generally encouraged, to increase the chance of detecting any toxicity to be monitored during Phase 1 and 2 human clinical trials. The purpose of this subcontract is to identify and evaluate the clinical potential of candidate targeted nanotherapeutics which has shown promise in small animal models for subsequent efficacy and toxicity testing in large animal models. It is expected that data gathered under this subcontract will enable filing of Investigational New Drug (IND) applications with the US-FDA.
 
Web Link
FBO.gov Permalink
(https://www.fbo.gov/spg/HHS/NIH/FCRF/S10-155/listing.html)
 
Place of Performance
Address: Subcontractor's location, United States
 
Record
SN02158208-W 20100526/100524234549-7599dd43df73858d9f00985a17337f45 (fbodaily.com)
 
Source
FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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