直 Japanese PDF Font
  • 弁護士等
  • 業務内容
  • 論文等
  • オフィス
  • 事務所概要
  • 採用情報
Finnegan
  • Articles & Books
    • Ad Law Buzz Blog
    • At the PTAB Blog
    • European IP Blog
    • CAFC控訴審関連ブログ
    • INCONTESTABLE® Blog
    • 出願関連ブログ
  • Events & Webinars
  • 知財最新ニュース
  • ポッドキャスト
    • AI + Finnegan
    • AI + Copyright
    • AI + Patent
    • AI + Privacy
    • AI + Trade Secrets
    • AI + Trademark
  • Unified Patent Court (UPC) Hub

Federal Circuit Denies En Banc Review of Amgen v. Sandoz, Leaving Intact the Panel Decision Interpreting Disclosure and Notice Provisions of the BPCIA

October 19, 2015

By Jeffrey D. Smyth

On October 16, 2015, the Federal Circuit declined to rehear en banc the July 21, 2015, decision in Amgen Inc. v. Sandoz Inc.1  Accordingly, the first Federal Circuit decision interpreting certain provisions of the Biologics Price Competition and Innovation Act (BPCIA) remains undisturbed.

In July, Judge Lourie wrote the decision for a split panel that also included Judges Newman and Chen. The decision resolved two main issues of first impression related to the BPCIA: (1) whether a biosimilar applicant must provide the reference product sponsor with a copy of its application to the FDA for licensure of its biosimilar product (aBLA), and (2) whether the biosimilar applicant must wait until it receives FDA approval before providing the reference product sponsor with its 180-day notice of commercial marketing.

With regard to the first issue, Judges Lourie and Chen agreed that the aBLA disclosure provision set forth in §262(l)(2) of the BPCIA is optional.2  The decision rejected Amgen’s argument that use of the word “shall” in § 262(l)(2) indicated that disclosure of the aBLA was mandatory, finding instead that when read in context with other provisions of the BPCIA, the aBLA disclosure provision was optional.3  Judge Newman dissented.

With regard to the second issue, Judges Lourie and Newman agreed that a biosimilar applicant could not provide its 180-day notice of commercial marketing until after the FDA approves the biosimilar application, rejecting Sandoz’s argument to the contrary. Judge Lourie explained that before FDA approval, the therapeutic uses and manufacturing processes of a potential biosimilar are not fixed, and thus a biosimilar applicant cannot give effective notice until after the FDA has granted approved.4,5  Judge Chen dissented.

Having each lost on one issue, both Amgen and Sandoz filed petitions for rehearing. Based on the fractured nature of the panel decision, many watching the case anticipated en banc review. By denying the petitions, the court’s July decision remains intact. Either side may appeal the decision to the United States Supreme Court, and given the significant implications stemming from the Federal Circuit’s decision, petitions seeking certiorari can be expected.

 

Endnotes
1Amgen Inc. v. Sandoz Inc., 794 F.3d 1347 (Fed. Cir. 2015).

2Id. at 1355-56.

3Id.

4Id. at 1357.

5Id. at 1358-59.

 

Tags

Amgen Inc. v. Sandoz Inc., Biologics Price Competition and Innovation Act (BPCIA), Food and Drug Administration (FDA), United States Court of Appeals for the Federal Circuit (CAFC)

Related Industries

ライフサイエンス

Biologics

Related Professionals

Jeffrey D. Smyth
Partner
Palo Alto, CA
+1 650 849 6618
Email

Copyright © Finnegan, Henderson, Farabow, Garrett & Dunner, LLP. This article is for informational purposes, is not intended to constitute legal advice, and may be considered advertising under applicable state laws. This article is only the opinion of the authors and is not attributable to Finnegan, Henderson, Farabow, Garrett & Dunner, LLP, or the firm's clients.

Related Insights

Conference

IAM Live: Navigating the UPC 2026

November 3, 2026

Paris

Conference

4th Global Patent Litigation FORUM

October 29, 2026

Munich

Hybrid Conference

Intellectual Property Law Institute 2026 – California

October 19-20, 2026

San Francisco

Hybrid Conference

Intellectual Property Law Institute 2026 – New York

September 28-29, 2026

New York

Conference

13th Annual Summit for Women Leaders in Life Sciences Law

July 29-30, 2026

Boston

Webinar

U.S. Patent Case Law Update 2026

July 23, 2026

Webinar

Webinar

Successful Strategies to Win Alice Motions and Fee Awards in Patent Cases Against Non-Practicing Entities

July 22, 2026

Webinar

Webinar

Early Motions in Trade Secret Litigation – Offensive and Defensive Insights

July 15, 2026

Webinar

Federal Circuit IP Blog

“2” Does Not Provide Written Description Support for “1”: Federal Circuit Affirms District Court’s Invalidation of Patent

July 8, 2026

Due to international data regulations, we’ve updated our privacy policy. Click here to read our privacy policy in full.

  • プライバシー
  • 免責事項
  • Legal Notices
  • Fraud Alert
  • EEO Statement
  • Cookies
  • Contact Us

© 2026 Finnegan, Henderson, Farabow, Garrett & Dunner, LLP