36C24E22Q0013.docx

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AN11--Intent to Sole Source: Investigational New Drug Request - Imiquid & Placebo cream
Solicitation number
36C24E22Q0013
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SUBJECT*

Intent to Sole Source: Investigational New Drug Request - Imiquid & Placebo cream

GENERAL INFORMATION

CONTRACTING OFFICE’S ZIP CODE*
15212-5319
SOLICITATION NUMBER*
36C24E22Q0013
ARCHIVE
99 DAYS AFTER THE RESPONSE DATE
RECOVERY ACT FUNDS
N
PRODUCT SERVICE CODE*
AN11
NAICS CODE*
541715
CONTRACTING OFFICE ADDRESS
US Department of Veterans Affairs

Veterans Health Administration Regional Procurement Office (RPO) East 323 North Shore Drive, Suite 500 Pittsburgh PA 15212-5319

POINT OF CONTACT*

lynn.portman@va.gov

ADDITIONAL INFORMATION

AGENCY’S URL

URL DESCRIPTION

AGENCY CONTACT’S EMAIL ADDRESS

EMAIL DESCRIPTION

Special Notice Special Notice

DESCRIPTION

*= Required Field
Special Notice

Special Notice

The Department of Veterans Affairs, VA Cooperative Studies Program, Clinical Research Pharmacy Coordinating Center (CRPCC) in Albuquerque, NM, intends to negotiate on a sole source basis, pursuant to FAR 6.302-1, with Irisys Inc provide ACTIVE Imiquimod 5% cream and matching PLACEBO products to CRPCC for up to a three-year period. The vendor is also required to develop required formulations and analytic methods related to successful manufacturing of the product which will be submitted to the FDA as part of the Investigational New Drug (IND) request. Irisys was the only vendor identified who was a FDA-approved Manufacturer and could formulate, manufacture, and supply the CSPCRPCC with active Imiquimod (IMQ) 5% topical cream with a therapeutic equivalence evaluation and a matching placebo and the vendor. Therapeutic equivalency requires that the active IMQ 5% cream be classified as a pharmaceutical equivalent, expected to have the same clinical effect and safety profile when administered to study participants under the conditions specified in the official prescribing information. Irisys will develop active and placebo formulations and provide it to user for submission in FDA Investigational New Drug (IND) application. This requirement is supporting a cancer prevention clinical study intending to use imiquimod 5% cream and matching placebo as the drug intervention. This trial will study the effects of chemoprevention on the recurrence of basal cell carcinoma. This is a notice of intent and is not a request for competitive proposals; however, any responsible source who believes it is capable of meeting the requirement may submit a capability statement to the contracting office no later than November 9th, 12PM, EST. Interest/capability statements may be sent to Lynn Portman at lynn.portman@va.gov. No telephone responses will be accepted. A determination not to compete the proposed requirement based upon the responses to this notice is solely within the discretion of the Government.

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