Finding against the Federal Circuit once again on a patent case, the Supreme Court issued a unanimous decision in Sandoz v. Amgen relating to the interpretation of the Biologics Price Competition and Innovation Act of 2009 ("BPCIA") in its first decision on the Act. The Supreme Court's decision firmly establishes the availability of a third biosimilar "dance," at least as far as Federal law is concerned.

The BPCIA provides the mechanism by which companies can bring to market "biosimilar" compounds, i.e., products that can compete with biological drugs much the same way as generic drugs compete with traditional "brand" pharmaceutical products. On appeal, the Supreme Court considered two issues. First, the biosimilar applicant, Sandoz, challenged the Federal Circuit's interpretation of the BPCIA as requiring an applicant to wait until after the FDA approved its biosimilar application before providing the requisite 180-day notice of commercial marketing to the brand company. This meant that a biosimilar applicant had to wait an additional 180 days after its application was granted before it could launch a competing product. The FDA cannot approve ("license") a biosimilar product until twelve years after the biologic was first approved by the agency. Thus, the Federal Circuit's decision effectively provided the brand manufacturer with 12½ years rather than 12 years of market exclusivity.

The Supreme Court reversed the Federal Circuit and explicitly determined that applicants can provide notice before or after FDA approval. According to the Supreme Court, the pertinent statutory language in the BPCIA has two separate requirements: (1) that the biosimilar application is "licensed" before it is marketed; and (2) that the biosimilar applicant gives notice 180 days before marketing occurs. The Federal Circuit thus erred in requiring licensure before notice could be given.

The second issue tackled by the Supreme Court relates to the "patent dance" provisions of the BPCIA. The "patent dance" is a statutory scheme through which the biosimilar applicant and the brand manufacturer exchange information and legal theories until deciding upon which patents to litigate first. Sandoz refused to provide the biosimilar application and manufacturing information contemplated in the dance, leading Amgen to seek an injunction under federal and state law to compel participation. The district court and Federal Circuit determined that an injunction was not available.

On cross-appeal, the Supreme Court agreed with the Federal Circuit that injunctions under federal law are not permitted, but remanded the case to review state law remedies. According to the Court, the BPCIA allows the brand company immediately to bring a declaratory judgment action against the biosimilar applicant if they do not provide their application and manufacturing information. This remedy deprives the applicant of the ability to control the scope of the litigation (i.e., which patents to litigate) and the timing of the suit. The Supreme Court determined that the remedy of immediate suit was the only federal remedy contemplated for an applicant's failure to dance. The Supreme Court remanded the case to address whether non-compliance with the BPCIA can be considered a violation of California law entitling Amgen to an injunction and/or whether the BPCIA's remedy pre-empts any state law remedies.

Seyfarth will be closely monitoring the remand of Sandoz in the coming months.

The SANDOZ Dance

Step 1: Skip
42 U.S.C. § 262(l)(2)(A)
Applicant refuses to provide aBLA and information describing manufacturing
Step 2: File Suit
42 U.S.C. § 262(l)(9)(C)
Reference sponsor chooses what patents to sue upon and when to bring suit against Applicant

The FAST BPCIA Dance

Step 1: Disclose
42 U.S.C. § 262(l)(2)(A) – 20 days
Applicant provides a copy of aBLA and information describing manufacturing
Step 2: Disclose
42 U.S.C. § 262(l)(3)(A) – 60 days
Reference sponsor provides list of assertable patents and identifies any patents it is willing to license
Step 3: Disclose
42 U.S.C. § 262(l)(3)(B) – 60 days
Applicant provides its own list of assertable patents, responds to licensing offer, and gives "detailed statements" why all listed patents are invalid, unenforceable, or will not be infringed
Step 4: Disclose
42 U.S.C. § 262(l)(3)(C) – 60 days
Reference sponsor gives "detailed statements" why the claims of all listed patents are infringed and responds to Applicant's detailed statements
Step 5: Negotiate
42 U.S.C. § 262(l)(4)(A)
Applicant and Reference sponsor negotiate to develop a final and complete list of patents for the initial patent infringement lawsuit and agree
Step 6: File Suit42 U.S.C. § 262(l)(6)(A) – 30 days Reference sponsor files suit on agreed-upon patents

The SLOW BPCIA Dance

Step 1: Disclose
42 U.S.C. § 262(l)(2)(A) – 20 days
Applicant provides a copy of aBLA and information describing manufacturing
Step 2: Disclose
42 U.S.C. § 262(l)(3)(A) – 60 days
Reference sponsor provides list of assertable patents and identifies any patents it is willing to license
Step 3: Disclose
42 U.S.C. § 262(l)(3)(B) – 60 days
Applicant provides its own list of assertable patents, responds to licensing offer, and gives "detailed statements" why all listed patents are invalid, unenforceable, or will not be infringed
Step 4: Disclose
42 U.S.C. § 262(l)(3)(C) – 60 days
Reference sponsor gives "detailed statements" why the claims of all listed patents are infringed and responds to Applicant's detailed statements
Step 5: Negotiate
42 U.S.C. § 262(l)(4)(B) – 15 days
Applicant and Reference sponsor negotiate to develop a final and complete list of patents for the initial patent infringement lawsuit but FAIL TO agree
Step 6: Choose
42 U.S.C. § 262(l)(5)(A)
Applicant gives reference sponsor the number of patents it proposes to litigate
Step 7: Exchange
42 U.S.C. § 262(l)(5)(B) – 5 days
Applicant and Reference sponsor simultaneously exchange list of patents that should be part of infringement action; Reference sponsor's list limited to same number given by Applicant
Step 8: File Suit
42 U.S.C. § 262(l)(6)(B) – 30 days
Reference sponsor files suit on all patents on lists.

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