New Jersey 2022-2023 Regular Session

New Jersey Senate Bill S1030

Introduced
1/31/22  

Caption

Permits certain managed care organizations to consider cost-effectiveness when placing prescription drug on formulary.

Impact

The impact of Bill S1030 on state laws is significant as it modifies the existing framework regulating MCOs and Medicaid drug formularies. By allowing cost-effectiveness to be considered in the decision-making process for drug formulary inclusion, the bill introduces a new layer of evaluation that MCOs can utilize to navigate the financial aspects of drug coverage. This could lead to a more economically sustainable approach to managing Medicaid services, although it must operate within the regulations already established by federal law, which prohibits MCOs from denying drug coverage solely based on cost.

Summary

Bill S1030, introduced in the New Jersey Legislature, addresses the operation of managed care organizations (MCOs) by permitting them to factor in cost-effectiveness data when developing formularies for prescription drugs. This legislation specifically applies to MCOs that contract with the Division of Medical Assistance and Health Services to provide pharmacy services to Medicaid-eligible individuals. The bill aims to create a more flexible framework for MCOs to manage drug listings, enhancing their ability to potentially control healthcare costs while ensuring that clinical efficacy and safety remain priority considerations.

Contention

Notably, there are concerns related to this bill. Critics may argue that emphasizing cost-effectiveness could inadvertently lead to restricting access to certain medications for Medicaid recipients if MCOs prioritize cheaper alternatives over potentially more effective treatment options. Such a shift could impact patient outcomes negatively, particularly if the cost-effective alternatives do not meet the clinical needs of all patients. Therefore, while the bill seeks to encourage prudent financial management within Medicaid, it must balance this goal against the imperative to safeguard patient access to necessary and effective medications.

Companion Bills

No companion bills found.

Previously Filed As

NJ S0117

Sets controls on Medicaid prescription drug costs by imposing transparency and accountability requirements on managed care organizations (MCOs) and their pharmacy benefit managers (PBMs).

NJ H5463

Sets controls on Medicaid prescription drug costs by imposing transparency and accountability requirements on managed care organizations (MCOs) and their pharmacy benefit managers (PBMs).

NJ H7692

Sets controls on Medicaid prescription drug costs by imposing transparency and accountability requirements on managed care organizations (MCOs) and their pharmacy benefit managers (PBMs).

NJ HB2329

Health insurance; prescription drug formularies.

NJ A1821

Prohibits health insurance carriers from denying coverage of nonopioid prescription drugs in favor of opioid prescription drugs.

NJ SB393

Health Insurance - Prescription Drug Formularies and Coverage for Generic Drugs and Biosimilars

NJ HB529

Health Insurance - Prescription Drug Formularies and Coverage for Generic Drugs and Biosimilars

NJ A2771

Permits import of prescription drugs from certain countries.

NJ SB00196

An Act Limiting Changes To Prescription Drug Formularies For Psychiatric Prescription Drugs.

NJ A3406

Establishes prescription drug pricing disclosure requirements and measures to reduce prescription drug costs.

Similar Bills

IN SB0140

Pharmacy benefits.

FL H0697

Drug Prices and Coverage

NJ A1821

Prohibits health insurance carriers from denying coverage of nonopioid prescription drugs in favor of opioid prescription drugs.

IL SB1390

DHFS-MCO-PBM-CONTRACTS

LA HB920

Requires drug manufacturers to limit pricing of GLP-1 medications for health insurance plans (OR INCREASE GF EX See Note)

AR HB1186

To Create The Pain Relief Parity Act; And To Require Pain Relief Parity In The Arkansas Medicaid Program.

NJ A1510

Improves access to lower cost generic and biosimilar drugs and revises certain requirements regarding dispensing of biosimilar drugs by pharmacies.*

MT HB774

Generally revise laws relating to pharmacies