AB50,1460,1713(3) Patient assistance program. (a) Establishment of program. No later 14than July 1, 2026, each manufacturer shall establish a patient assistance program 15to make insulin available in accordance with this subsection to individuals who 16meet the eligibility requirements under par. (b). Under the patient assistance 17program, the manufacturer shall do all of the following: AB50,1460,20181. Provide the commissioner with information regarding the patient 19assistance program, including contact information for individuals to call for 20assistance in accessing the patient assistance program. AB50,1460,22212. Provide a hotline for individuals to call or access between 8 a.m. and 10 p.m. 22on weekdays and between 10 a.m. and 6 p.m. on Saturdays. AB50,1461,2
13. List the eligibility requirements under par. (b) on the manufacturer’s 2website. AB50,1461,634. Maintain the privacy of all information received from an individual 4applying for or participating in the patient assistance program and not sell, share, 5or disseminate the information unless required under this section or authorized, in 6writing, by the individual. AB50,1461,87(b) Eligible individual. An individual shall be eligible to receive insulin under 8a patient assistance program if all of the following conditions are met: AB50,1461,991. The individual is a resident of this state. AB50,1461,12102. The individual, or the individual’s parent or legal guardian if the individual 11is under the age of 18, has a valid Wisconsin driver’s license or state identification 12card. AB50,1461,13133. The individual has a valid insulin prescription. AB50,1461,16144. The family income of the individual does not exceed 400 percent of the 15poverty line as defined and revised annually under 42 USC 9902 (2) for a family the 16size of the individual’s family. AB50,1461,17175. The individual is not receiving public assistance under ch. 49. AB50,1461,23186. The individual is not eligible to receive health care through a federally 19funded program or receive prescription drug benefits through the U.S. department 20of veterans affairs, except that this subdivision does not apply to an individual who 21is enrolled in a policy under Part D of Medicare under 42 USC 1395w-101 et seq. if 22the individual has spent at least $1,000 on prescription drugs in the current 23calendar year. AB50,1462,5
17. The individual is not enrolled in prescription drug coverage through an 2individual or group health plan that limits the total cost sharing amount, including 3copayments, deductibles, and coinsurance, that an enrollee is required to pay for a 430-day supply of insulin to no more than $75, regardless of the type or amount of 5insulin needed. AB50,1462,156(c) Application for patient assistance program. 1. An individual may apply to 7participate in a patient assistance program by filing an application with the 8manufacturer that established the patient assistance program, the individual’s 9health care practitioner if the practitioner participates in the patient assistance 10program, or a navigator included on the list under sub. (8) (c). A health care 11practitioner or navigator shall immediately submit the application to the 12manufacturer. Upon receipt of an application, the manufacturer shall determine 13the individual’s eligibility under par. (b) and, except as provided in subd. 2., notify 14the individual of the determination no later than 10 days after receipt of the 15application. AB50,1462,21162. If necessary to determine the individual’s eligibility under par. (b), the 17manufacturer may request additional information from an individual who has filed 18an application under subd. 1. no later than 5 days after receipt of the application. 19Upon receipt of the additional information, the manufacturer shall determine the 20individual’s eligibility under par. (b) and notify the individual of the determination 21no later than 3 days after receipt of the requested information. AB50,1463,4223. Except as provided in subd. 5., if the manufacturer determines under subd. 231. or 2. that the individual is eligible for the patient assistance program, the
1manufacturer shall provide the individual with a statement of eligibility. The 2statement of eligibility shall be valid for 12 months and may be renewed upon a 3determination by the manufacturer that the individual continues to meet the 4eligibility requirements under par. (b). AB50,1463,1554. If the manufacturer determines under subd. 1. or 2. that the individual is 6not eligible for the patient assistance program, the manufacturer shall provide the 7reason for the determination in the notification under subd. 1. or 2. The individual 8may appeal the determination by filing an appeal with the commissioner that shall 9include all of the information provided to the manufacturer under subds. 1. and 2. 10The commissioner shall establish procedures for deciding appeals under this 11subdivision. The commissioner shall issue a decision no later than 10 days after the 12appeal is filed, and the commissioner’s decision shall be final. If the commissioner 13determines that the individual meets the eligibility requirements under par. (b), the 14manufacturer shall provide the individual with the statement of eligibility 15described in subd. 3. AB50,1464,2165. In the case of an individual who has prescription drug coverage through an 17individual or group health plan, if the manufacturer determines under subd. 1. or 2. 18that the individual is eligible for the patient assistance program but also 19determines that the individual’s insulin needs are better addressed through the use 20of the manufacturer’s copayment assistance program rather than the patient 21assistance program, the manufacturer shall inform the individual of the 22determination and provide the individual with the necessary coupons to submit to
1a pharmacy. The individual may not be required to pay more than the copayment 2amount specified in par. (d) 2. AB50,1464,93(d) Provision of insulin under a patient assistance program. 1. Upon receipt 4from an individual of the eligibility statement described in par. (c) 3. and a valid 5insulin prescription, a pharmacy shall submit an order containing the name of the 6insulin and daily dosage amount to the manufacturer. The pharmacy shall include 7with the order the pharmacy’s name, shipping address, office telephone number, 8fax number, email address, and contact name, as well as any days or times when 9deliveries are not accepted by the pharmacy. AB50,1464,18102. Upon receipt of an order meeting the requirements under subd. 1., the 11manufacturer shall send the pharmacy a 90-day supply of insulin, or lesser amount 12if requested in the order, at no charge to the individual or pharmacy. The pharmacy 13shall dispense the insulin to the individual associated with the order. The insulin 14shall be dispensed at no charge to the individual, except that the pharmacy may 15collect a copayment from the individual to cover the pharmacy’s costs for processing 16and dispensing in an amount not to exceed $50 for each 90-day supply of insulin. 17The pharmacy may not seek reimbursement from the manufacturer or a 3rd-party 18payer. AB50,1464,21193. The pharmacy may submit a reorder to the manufacturer if the individual’s 20eligibility statement described in par. (c) 3. has not expired. The reorder shall be 21treated as an order for purposes of subd. 2. AB50,1465,2224. Notwithstanding subds. 2. and 3., a manufacturer may send the insulin
1directly to the individual if the manufacturer provides a mail-order service option, 2in which case the pharmacy may not collect a copayment from the individual. AB50,1465,53(4) Exceptions. (a) This section does not apply to a manufacturer that shows 4to the commissioner’s satisfaction that the manufacturer’s annual gross revenue 5from insulin sales in this state does not exceed $2,000,000. AB50,1465,106(b) A manufacturer may not be required to make an insulin product available 7under sub. (2) or (3) if the wholesale acquisition cost of the insulin product does not 8exceed $8, as adjusted annually based on the U.S. consumer price index for all 9urban consumers, U.S. city average, per milliliter or the applicable national council 10for prescription drug programs’ plan billing unit. AB50,1465,1311(5) Confidentiality. All medical information solicited or obtained by any 12person under this section shall be subject to the applicable provisions of state law 13relating to confidentiality of medical information, including s. 610.70. AB50,1465,1914(6) Reimbursement prohibition. No person, including a manufacturer, 15pharmacy, pharmacist, or 3rd-party administrator, as part of participating in an 16urgent need safety net program or patient assistance program may request or seek, 17or cause another person to request or seek, any reimbursement or other 18compensation for which payment may be made in whole or in part under a federal 19health care program, as defined in 42 USC 1320a-7b (f). AB50,1465,2220(7) Reports. (a) Annually, no later than March 1, each manufacturer shall 21report to the commissioner all of the following information for the previous calendar 22year: AB50,1466,2
11. The number of individuals who received insulin under the manufacturer’s 2urgent need safety net program. AB50,1466,532. The number of individuals who sought assistance under the 4manufacturer’s patient assistance program and the number of individuals who 5were determined to be ineligible under sub. (3) (c) 4.