H.R.3059 - Creating Hope Act of 2011112th Congress (2011-2012)
|Sponsor:||Rep. McCaul, Michael T. [R-TX-10] (Introduced 09/23/2011)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 09/26/2011 Referred to the Subcommittee on Health. (All Actions)|
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Summary: H.R.3059 — 112th Congress (2011-2012)All Information (Except Text)
Introduced in House (09/23/2011)
Creating Hope Act of 2011 - Amends the Federal Food, Drug, and Cosmetic Act to revise the priority review voucher program for tropical diseases to: (1) include rare pediatric diseases; (2) allow unlimited transfers of vouchers under the program; and (3) require a sponsor intending to use a voucher to notify the Secretary of Health and Human Services (HHS) at least 90 days (currently, 365 days) before submission of the application.
Revises provisions regarding the priority review user fee, including to make it payable upon notification of the Secretary of intent to use the voucher.
Authorizes the Secretary, upon request of the manufacturer or sponsor of a new drug, to designate that a new drug is: (1) for a rare pediatric disease, and (2) an eligible treatment.
Requires the Secretary to deem a rare pediatric disease product application to be incomplete if it does not contain a description of the sponsor's plan to market the product in the United States. Authorizes the Secretary to refuse to issue a priority review voucher upon the approval of a rare pediatric disease application if the Secretary finds that the sponsor lacks a good faith intention to market the product in the United States. Directs the Secretary to issue a guidance document setting forth the evidentiary support necessary to demonstrate such a good faith intention.
Requires sponsors of applications under the priority review voucher program to report to the Secretary within five years after the approval of the application on the demand and distribution of the product within the United States.