Us Congress 2025-2026 Regular Session

Us Congress Senate Bill SB2658

Introduced
8/1/25  

Caption

Medication Affordability and Patent Integrity Act

Impact

If enacted, SB2658 would significantly alter the current landscape of drug approval and patent processes in the pharmaceutical industry. By mandating that patent-related submissions to the FDA be consistent with those made to the USPTO, the bill is designed to facilitate a more streamlined operation between these two entities. This could prevent situations where conflicting information arises, potentially obstructing the patent approval process or leading to patent disputes. As a result, the bill may contribute to lower medication costs for consumers by fostering efficiency and clarity in drug market regulations.

Summary

SB2658, titled the 'Medication Affordability and Patent Integrity Act', aims to enhance transparency within the medical and pharmaceutical industries by requiring sponsors of drug applications and patent holders to submit specific information to both the Food and Drug Administration (FDA) and the United States Patent and Trademark Office (USPTO). The bill stipulates that any applicable patent must be certified and submitted alongside drug applications to ensure consistency in the information provided between these two regulatory bodies. This legislative move seeks to close gaps that may lead to discrepancies in drug patent applications and approvals.

Contention

While proponents of SB2658 argue that it is a necessary step towards greater accountability and oversight in the pharmaceutical industry, there are concerns regarding the implications for innovation. Critics may contend that the additional requirements could hinder smaller pharmaceutical companies from entering the market due to increased regulatory burdens. Moreover, the bill's requirements for data submission raise questions about intellectual property rights and the commercial confidentiality of sensitive information. Balancing the need for transparency with the protection of proprietary information will be a critical point of contention as the bill progresses through the legislative process.

Companion Bills

No companion bills found.

Previously Filed As

US SB2780

Medication Affordability and Patent Integrity Act

US HB5429

Medication Affordability and Patent Integrity Act

US SB4845

Prescription Drug Affordability and Access Act

US SB79

Interagency Patent Coordination and Improvement Act of 2023 This bill establishes the Interagency Task Force on Patents to support coordination and communication between the U.S. Patent and Trademark Office (PTO) and the Food and Drug Administration (FDA) on activities relating to patents for human drugs and biological products. The task force's duties shall include sharing information about (1) the processes of each agency, including how each agency evaluates applications (e.g., patent applications at the PTO and new drug applications at the FDA); and (2) new approvals of patents, human drugs, biological products, and new technologies. The task force must also establish a process that requires (1) the PTO to request from the FDA information relating to certain patent applications to help patent examiners carry out their duties, (2) the FDA to provide such information to the PTO, and (3) the PTO to assist the FDA in its ministerial role of listing patents.

US HB1717

Interagency Patent Coordination and Improvement Act of 2023

US HB9070

Affordable Prescriptions for Patients Act of 2024

US SB4674

Content Origin Protection and Integrity from Edited and Deepfaked Media Act of 2024

US SB4722

Furthering Operations for Resiliency, Transparency, and Integrity to Fortify (FORTIFY) United States Research Act Research Integrity and Security Act of 2024

US SB150

Affordable Prescriptions for Patients Act of 2023

US HB4893

Scientific Integrity Act

Similar Bills

No similar bills found.