H.R. 9192House119th Congress (2025-2027)In Committee

Prior Authorization Reform for Autoimmune and Blood Disorders Act

Introduced June 8, 2026

AI-Generated Summary

Updated June 16, 2026 at 7:21 PM UTC

The Prior Authorization Reform for Autoimmune and Blood Disorders Act would require group health plans and health‑insurance issuers to cover any drug used to treat an autoimmune disease, hemophilia, or von Willebrand disease. It also limits how often insurers can require prior authorization for those drugs, allowing only one request per 12‑month period except for short‑term drugs, certain controlled substances, or drugs subject to a REMS. The changes apply to plans beginning on or after January 1 2027.

Key Provisions

  • Adds a new ERISA provision (Sec. 727) that obligates group health plans and insurers to cover autoimmune or blood‑disorder drugs and restricts prior‑authorization requests to once per year, with limited exceptions.
  • Creates a matching requirement in the Public Health Service Act (Sec. 2799A‑12) with the same coverage and prior‑authorization limits.
  • Amends the Internal Revenue Code (Sec. 9827) to impose the same coverage and prior‑authorization rules on qualified health plans for tax purposes.
  • Defines “autoimmune or blood disorder drug” as any drug or biologic prescribed for an autoimmune disease, hemophilia, or von Willebrand disease.
  • Sets the effective date for all new requirements to plan years starting on or after January 1 2027.

Legislative Activity

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HouseIntro Referral Latest Action

Referred to the Committee on Energy and Commerce, and in addition to the Committees on Education and Workforce, and Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

June 8, 2026

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HouseIntro Referral

Introduced in House

June 8, 2026

HouseIntro Referral

Referred to the Committee on Energy and Commerce, and in addition to the Committees on Education and Workforce, and Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

June 8, 2026

Bill Text

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Introduced in HouseIssued June 8, 2026

I

119th CONGRESS

2d Session

H. R. 9192

IN THE HOUSE OF REPRESENTATIVES

June 8, 2026

Ms. Johnson of Texas (for herself and Mr. Lawler) introduced the following bill; which was referred to the Committee on Energy and Commerce, and in addition to the Committees on Education and Workforce, and Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned

A BILL

To amend the Employee Retirement Income Security Act of 1974, title XXVII of the Public Health Service Act, and the Internal Revenue Code of 1986 to require health insurance coverage of drugs indicated for the treatment of autoimmune diseases and certain blood disorders.

1.

Short title

This Act may be cited as the Prior Authorization Reform for Autoimmune and Blood Disorders Act.

2.

Requiring coverage of drugs indicated for the treatment of autoimmune diseases and certain blood disorders

(a)

ERISA amendments

(1)

In general

Subpart B of part 7 of subtitle B of title I of the Employee Retirement Income Security Act of 1974 (29 U.S.C. 1185 et seq.) is amended by adding at the end the following new section:

727.

Requirements with respect to coverage of drugs for autoimmune diseases and certain blood disorders

(a)

In general

A group health plan, and a health insurance issuer offering group health insurance coverage—

(1)

shall provide coverage for any drug that is an autoimmune or blood disorder drug, without regard to whether such drug is dispensed by a pharmacy or furnished incident to another item or service for which benefits are available under such plan or coverage; and

(2)

may not require, with respect to an individual enrolled under such plan or coverage, that prior authorization for such a drug be obtained more than once during any 12-month period unless such drug is—

(A)

typically used for a period of 12 months or less;

(B)

an opioid, a benzodiazepine, a barbiturate, or carisoprodol; or

(C)

a drug with respect to which a risk evaluation and mitigation strategy is required under Section 505–1 of the Federal Food, Drug, and Cosmetic Act.

(b)

Autoimmune or blood disorder drug defined

In this section, the term autoimmune or blood disorder drug means a drug or biological product that is indicated and prescribed for the treatment of an autoimmune disease, hemophilia, or Von Willebrand disease.

.

(2)

Clerical amendment

The table of contents in section 1 of the Employee Retirement Income Security Act of 1974 (29 U.S.C. 1001 et seq.) is amended by inserting after the item relating to section 726 the following:

Sec. 727. Requirements with respect to coverage of drugs for autoimmune diseases and certain blood disorders.

.

(b)

Public Health Service Act amendments

Part D of title XXVII of the Public Health Service Act (42 U.S.C. 300gg–111 et seq.) is amended by adding at the end the following new section:

2799A–12.

Requirements with respect to coverage of drugs for autoimmune diseases and certain blood disorders

(a)

In general

A group health plan, and a health insurance issuer offering group or individual health insurance coverage—

(1)

shall provide coverage for any drug that is an autoimmune or blood disorder drug, without regard to whether such drug is dispensed by a pharmacy or furnished incident to another item or service for which benefits are available under such plan or coverage; and

(2)

may not require, with respect to an individual enrolled under such plan or coverage, that prior authorization for such a drug be obtained more than once during any 12-month period unless such drug is—

(A)

typically used for a period of 12 months or less;

(B)

an opioid, a benzodiazepine, a barbiturate, or carisoprodol; or

(C)

a drug with respect to which a risk evaluation and mitigation strategy is required under Section 505–1 of the Federal Food, Drug, and Cosmetic Act.

(b)

Autoimmune or blood disorder drug defined

In this section, the term autoimmune or blood disorder drug means a drug or biological product that is indicated and prescribed for the treatment of an autoimmune disease, hemophilia, or Von Willebrand disease.

.

(c)

Internal Revenue Code amendments

(1)

In general

Subchapter B of chapter 100 of the Internal Revenue Code of 1986 is amended by adding at the end the following new section:

9827.

Requirements with respect to coverage of drugs for autoimmune diseases and certain blood disorders

(a)

In general

A group health plan—

(1)

shall provide coverage for any drug that is an autoimmune or blood disorder drug, without regard to whether such drug is dispensed by a pharmacy or furnished incident to another item or service for which benefits are available under such plan; and

(2)

may not require, with respect to an individual enrolled under such plan, that prior authorization for such a drug be obtained more than once during any 12-month period unless such drug is—

(A)

typically used for a period of 12 months or less;

(B)

an opioid, a benzodiazepine, a barbiturate, or carisoprodol; or

(C)

a drug with respect to which a risk evaluation and mitigation strategy is required under Section 505–1 of the Federal Food, Drug, and Cosmetic Act.

(b)

Autoimmune or blood disorder drug defined

In this section, the term autoimmune or blood disorder drug means a drug or biological product that is indicated and prescribed for the treatment of an autoimmune disease, hemophilia, or Von Willebrand disease.

.

(2)

Clerical amendment

The table of sections for subchapter B of chapter 100 of the Internal Revenue Code of 1986 is amended by adding at the end the following new item:

Sec. 9827. Requirements with respect to coverage of drugs for autoimmune diseases and certain blood disorders.

.

(d)

Effective date

The amendments made by this section shall apply with respect to plan years beginning on or after January 1, 2027.