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| 1 | | "Hormonal therapy medication" means hormonal treatment |
| 2 | | administered to treat gender dysphoria. |
| 3 | | "Therapeutic equivalent version" means drugs, devices, or |
| 4 | | products that can be expected to have the same clinical effect |
| 5 | | and safety profile when administered to patients under the |
| 6 | | conditions specified in the labeling and that satisfy the |
| 7 | | following general criteria: |
| 8 | | (1) it is approved as safe and effective; |
| 9 | | (2) it is a pharmaceutical equivalent in that it: |
| 10 | | (A) contains identical amounts of the same active |
| 11 | | drug ingredient in the same dosage form and route of |
| 12 | | administration; and |
| 13 | | (B) meets compendial or other applicable standards |
| 14 | | of strength, quality, purity, and identity; |
| 15 | | (3) it is bioequivalent in that: |
| 16 | | (A) it does not present a known or potential |
| 17 | | bioequivalence problem and it meets an acceptable in |
| 18 | | vitro standard; or |
| 19 | | (B) if it does present such a known or potential |
| 20 | | problem, it is shown to meet an appropriate |
| 21 | | bioequivalence standard; |
| 22 | | (4) it is adequately labeled; and |
| 23 | | (5) it is manufactured in compliance with Current Good |
| 24 | | Manufacturing Practice regulations adopted by the United |
| 25 | | States Food and Drug Administration. |
| 26 | | (b) An individual or group policy of accident and health |
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| 1 | | insurance amended, delivered, issued, or renewed in this State |
| 2 | | on or after January 1, 2024 shall provide coverage for all |
| 3 | | abortifacients, hormonal therapy medication, human |
| 4 | | immunodeficiency virus pre-exposure prophylaxis, and |
| 5 | | post-exposure prophylaxis drugs approved by the United States |
| 6 | | Food and Drug Administration, and follow-up services related |
| 7 | | to that coverage, including, but not limited to, management of |
| 8 | | side effects, medication self-management or adherence |
| 9 | | counseling, risk reduction strategies, and mental health |
| 10 | | counseling. This coverage shall include drugs approved by the |
| 11 | | United States Food and Drug Administration that are prescribed |
| 12 | | or ordered for off-label use for the purposes described in |
| 13 | | this Section. On or after the effective date of this |
| 14 | | amendatory Act of the 104th General Assembly, this coverage |
| 15 | | shall include pre-PrEP HIV screening, sexually transmitted |
| 16 | | infection screening, kidney function analysis, routine |
| 17 | | laboratory testing, and routine provider visits. |
| 18 | | (c) The coverage required under subsection (b) is subject |
| 19 | | to the following conditions: |
| 20 | | (1) If the United States Food and Drug Administration |
| 21 | | has approved one or more therapeutic equivalent versions |
| 22 | | of an abortifacient drug, a policy is not required to |
| 23 | | include all such therapeutic equivalent versions in its |
| 24 | | formulary so long as at least one is included and covered |
| 25 | | without cost sharing and in accordance with this Section. |
| 26 | | (2) If an individual's attending provider recommends a |
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| 1 | | particular drug approved by the United States Food and |
| 2 | | Drug Administration based on a determination of medical |
| 3 | | necessity with respect to that individual, the plan or |
| 4 | | issuer must defer to the determination of the attending |
| 5 | | provider and must cover that service or item without cost |
| 6 | | sharing. |
| 7 | | (3) If a drug is not covered, plans and issuers must |
| 8 | | have an easily accessible, transparent, and sufficiently |
| 9 | | expedient process that is not unduly burdensome on the |
| 10 | | individual or a provider or other individual acting as a |
| 11 | | patient's authorized representative to ensure coverage |
| 12 | | without cost sharing. |
| 13 | | The conditions listed under this subsection (c) also apply |
| 14 | | to drugs prescribed for off-label use as abortifacients. |
| 15 | | (d) Except as otherwise provided in this Section, a policy |
| 16 | | subject to this Section shall not impose a deductible, |
| 17 | | coinsurance, copayment, or any other cost-sharing requirement |
| 18 | | on the coverage provided. The provisions of this subsection do |
| 19 | | not apply to coverage of procedures to the extent such |
| 20 | | coverage would disqualify a high-deductible health plan from |
| 21 | | eligibility for a health savings account pursuant to the |
| 22 | | federal Internal Revenue Code, 26 U.S.C. 223. |
| 23 | | (e) Except as otherwise authorized under this Section, a |
| 24 | | policy shall not impose any restrictions or delays on the |
| 25 | | coverage required under this Section. |
| 26 | | (f) The coverage requirements in this Section for |
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| 1 | | abortifacients do not, pursuant to 42 U.S.C. 18054(a)(6), |
| 2 | | apply to a multistate plan that does not provide coverage for |
| 3 | | abortion. |
| 4 | | (g) If the Department concludes that enforcement of any |
| 5 | | coverage requirement of this Section for abortifacients may |
| 6 | | adversely affect the allocation of federal funds to this |
| 7 | | State, the Department may grant an exemption to that |
| 8 | | requirement, but only to the minimum extent necessary to |
| 9 | | ensure the continued receipt of federal funds. |
| 10 | | (Source: P.A. 102-1117, eff. 1-13-23; 103-462, eff. 8-4-23.) |
| 11 | | Section 10. The Prior Authorization Reform Act is amended |
| 12 | | by adding Section 52 as follows: |
| 13 | | (215 ILCS 200/52 new) |
| 14 | | Sec. 52. Prior authorization for certain prescription |
| 15 | | drugs; prohibited. A health insurance issuer may not require |
| 16 | | prior authorization for the following prescription drug types |
| 17 | | and their therapeutic equivalents approved by the United |
| 18 | | States Food and Drug Administration: human immunodeficiency |
| 19 | | virus pre-exposure prophylaxis and post-exposure prophylaxis |
| 20 | | medication or human immunodeficiency virus treatment |
| 21 | | medication. This Section does not apply to a health care plan |
| 22 | | serving Medicaid populations that provides, arranges for, pays |
| 23 | | for, or reimburses the cost of any health care service for |
| 24 | | persons who are enrolled under the Illinois Public Aid Code; |
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| 1 | | however, nothing in this Section shall be construed to limit |
| 2 | | or otherwise diminish any coverage requirements, patient |
| 3 | | protections, or access standards applicable to the medical |
| 4 | | assistance program under the Illinois Public Aid Code, |
| 5 | | including, but not limited to, Section 5-5, Section 5-16.8, or |
| 6 | | any other provision of the Illinois Public Aid Code regarding |
| 7 | | coverage of human immunodeficiency virus pre-exposure |
| 8 | | prophylaxis and post-exposure prophylaxis medication or human |
| 9 | | immunodeficiency virus treatment medication. This Section does |
| 10 | | not apply to the State Employees Group Insurance Program or |
| 11 | | any health care plan established or maintained under the State |
| 12 | | Employees Group Insurance Act of 1971. |
| 13 | | Section 99. Effective date. This Act takes effect January |
| 14 | | 1, 2028.". |