Protecting America’s Life Saving Medicines Act of 2019
A BILL
To direct the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to conduct a study on high-risk, high-reward drugs, and for other purposes.
Sec. 2 Study on high-risk, high-reward drugs
Sec. 3 Credit for clinical testing expenses for certain high-risk, high-reward drugs
“45T. Clinical testing expenses for certain high-risk, high-reward drugs
“(a) In general—For purposes of section 38, the credit determined under this section for the taxable year is an amount equal to 25 percent of the qualified clinical testing expenses for the taxable year.
“(b) Qualified clinical testing expenses—For purposes of this section—
“(1) Qualified clinical testing expenses
“(A) In general—Except as otherwise provided in this paragraph, the term qualified clinical testing expenses means the amounts which are paid or incurred by the taxpayer during the taxable year which would be described in subsection (b) of section 41 if such subsection were applied with the modifications set forth in subparagraph (B).
“(B) Modifications—For purposes of subparagraph (A), subsection (b) of section 41 shall be applied—
“(i) by substituting “clinical testing” for “qualified research” each place it appears in paragraphs (2) and (3) of such subsection, and
“(ii) by substituting “100 percent” for “65 percent” in paragraph (3)(A) of such subsection.
“(C) Exclusion for amounts funded by grants, etc—The term qualified clinical testing expenses shall not include any amount to the extent such amount is funded by any grant, contract, or otherwise by another person (or any governmental entity).
“(2) Clinical testing—The term clinical testing means any human clinical testing—
“(A) which is carried out with respect to a drug on a list submitted to the Secretary under subsection (b) of the Protecting America’s Life Saving Medicines Act of 2019,
“(B) which occurs—
“(i) after the date such list is so submitted, and
“(ii) before the date on which an application with respect to such drug is approved under section 505(b) of such Act or, if the drug is a biological product, before the date on which a license for such drug is issued under section 351 of the Public Health Service Act.
“(c) Coordination with credit for increasing research expenditures
“(1) In general—Except as provided in paragraph (2), any qualified clinical testing expenses for a taxable year to which an election under this section applies shall not be taken into account for purposes of determining the credit allowable under section 41 for such taxable year.
“(2) Expenses included in determining base period research expenses—Any qualified clinical testing expenses for any taxable year which are qualified research expenses (within the meaning of section 41(b)) shall be taken into account in determining base period research expenses for purposes of applying section 41 to subsequent taxable years.
“(d) Special rules
“(1) Certain rules made applicable—Rules similar to the rules of paragraphs (1) and (2) of section 41(f) shall apply for purposes of this section.
“(2) Election—This section shall apply to any taxpayer for any taxable year only if such taxpayer elects (at such time and in such manner as the Secretary may by regulations prescribe) to have this section apply for such taxable year.”
“(33) the credit determined under section 45T.”