C. Factors Considered in Cost Review Study.
(1) To the extent practicable, the Board may
consider the following data, information, and analyses in conducting a cost
review study:
(a) Drug Pricing for Drug
Product Under Review:
(i) The WAC, AWP, NADAC,
SAAC, ASP, and FSS; and
(ii)
Information estimating manufacturer net price and net sales amounts of the
prescription drug product under review;
(b) Price Concessions, Discounts, and
Rebates:
(i) The average price concession,
discount, and rebate provided by the manufacturer or expected to be provided to
each payor class in the State for the drug under review, expressed as a number
and as a percent of the WAC; and
(ii) The average price concession, discount,
and rebate the manufacturer provided or is expected to provide for the
prescription drug product under review to each PBM operating in the State,
expressed as a number and as a percent of the WAC;
(c) Therapeutic Alternatives:
(i) The average price concession, discount,
or rebate the manufacturer provides or is expected to provide to health plans
in the State for therapeutic alternatives; and
(ii) The WAC, AWP, NADAC, SAAC, ASP, and FSS
at which each therapeutic alternative has been sold in the State;
(d) Patient Access:
(i) The costs to health plans based on
patient access consistent with FDA-labeled indications or standard medical
practice;
(ii) The estimated impact
on patient access resulting from the cost of the prescription drug product
relative to insurance benefit design; and
(iii) The current or expected dollar value of
drug-specific patient access programs that are supported by the
manufacturer;
(e) Cost
and Comparative Effectiveness Analyses:
(i)
The incremental costs associated with a prescription drug product, including
financial impacts to health, medical, or social services as can be quantified
and compared to baseline effects of existing therapeutic alternatives;
and
(ii) Information derived from
health economics and outcomes research that may address the effectiveness of
the prescription drug product in treating the conditions for which it is
prescribed or in improving a patient's health, quality of life, or overall
health outcomes, and the effectiveness of the prescription drug product
compared with therapeutic alternatives or no treatment.
(f) Cost Sharing:
(i) The average patient copay and other
cost-sharing data for the prescription drug in the State; and
(ii) The average cost share; and
(g) Additional Board Factors:
(i) Clinical information, including FDA
indications and doses and information concerning standard medical
practice;
(ii) The disease burden
of the condition that is treated by the prescription drug product;
(iii) In the case of generic prescription
drug products, the number of pharmaceutical manufacturers that produce the
prescription drug product;
(iv) The
total gross spending in the State for the prescription drug product under
review, the total number of patients in the State using the prescription drug
product, and the percentage of overall total prescription drug product spending
that the product's spending represents;
(v) The change in total gross spending and
utilization for a prescription drug product in the State between the two most
recent available calendar years and the percent change in total gross spending
for a prescription drug product in the State between the two most recent
available calendar years;
(vi) The
mean, median, and 90th percentile out-of-pocket costs per patient compared to
State incomes;
(vii) An assessment
of the impact of the prescription drug product's cost to access by priority
populations and the impact on equity;
(viii) Information supplied by the
manufacturer, if any, explaining the relationship between the pricing of the
prescription drug product and (a) the cost of development and (b) the
therapeutic benefit of the prescription drug product, or information that is
otherwise pertinent to the manufacturer's pricing decision;
(ix) Analysis of the prescription drug
product's approval process;
(x)
Analysis of the prescription drug product's shortage status;
(xi) Analysis of the prescription drug
product's lifecycle management, patent management, regulatory exclusivities,
and product copying;
(xii) Input
from the public; and
(xiii)
Information and analyses submitted by an entity under Regulation .04 of this
chapter.
(2)
The public may provide written comments concerning the prescription drug
product:
(a) Within 60 days of the date the
drug's selection for cost review study is posted on the Board's website;
and
(b) In accordance with the
procedures in COMAR
14.01.01.05B(3).