Cephalon, Inc. v. Abraxis Bioscience, LLC

618 F. App'x 663
CourtCourt of Appeals for the Federal Circuit
DecidedJune 17, 2015
Docket2014-1411, 2014-1442
StatusUnpublished
Cited by1 cases

This text of 618 F. App'x 663 (Cephalon, Inc. v. Abraxis Bioscience, LLC) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cephalon, Inc. v. Abraxis Bioscience, LLC, 618 F. App'x 663 (Fed. Cir. 2015).

Opinion

WALLACH, Circuit Judge.

Plaintiffs-appellants Acusphere, Inc. and Cephalon, Inc. (collectively, “Acusphere”) appeal certain claim construction determinations of the United States District Court for the District of Massachusetts with respect to a patent directed to formulations of, and methods of making, the anticancer drug product paclitaxel. In light of the district court’s construction, Acusphere • stipulated to a final judgment of non-infringement. Defendants-cross-appellants Abraxis Bioscience, LLC and Celgene Corp. (collectively, “Celgene”) cross-appeal, asserting certain claim terms of the patent are indefinite. Because the district court properly construed at least some of *664 the disputed terms, this court affirms and does not reach the indefiniteness issues presented by the cross-appeal.

BACKGROUND

Acusphere, Inc. is the assignee of U.S. Reissued Patent No. RE40,493 (“the '493 patent”), titled “Porous Paclitaxel Matrices and Methods of Manufacture Thereof.” Acusphere, Inc., and -its exclusive licensee Cephalon, Inc., sued Celgene for infringement of the '493 patent based on Celgene’s Abraxane drug product, which contains a fast-dissolving form of paclitaxel.

Paclitaxel is a type of taxane compound derived from the bark of the Pacific yew tree and exhibits “extremely low solubility in water,” '493 patent col. 1 11. 22-27, making effective administration challenging. The prior art. clinical formulation addressed this problem by the use of a solubilizing agent called Cremophor (poly-oxyethylated castor oil), but this agent can cause severe adverse reactions and requires infusion into the patient over several hours. The '493 patent addresses the solubility problem by integrating pa-clitaxel into a “porous matrix form which forms nanoparticles and microparticles of paclitaxel when the matrix is contacted with an aqueous medium.” Id. col. 1 1. 66-col. 2 1. 1.

Following the district court’s construction of a number of disputed claim terms, see Cephalon, Inc. v. Celgene Corp., 985 F.Supp.2d 171 (D.Mass.2013), Acusphere stipulated to noninfringement. Acusphere appeals the district court’s claim constructions of: (1) “nanoparticles” and “micro-particles”; (2) “nanoparticles and micro-particles of a taxane”; and (3) “wherein upon exposure to an aqueous medium, the matrix dissolves to leave the taxane nano-particles and microparticles.” See Appellants’ Br. 2-3. Acusphere stipulated that if any of the district court’s claim constructions are affirmed, it cannot sustain its burden of proving infringement of the '493 patent. J.A. 29. This court has jurisdiction under 28 U.S.C. § 1295(a)(1) (2012).

Discussion

I. Standard of Review.

This court reviews the district court’s •claim construction de novo, but “review[s] for clear error those factual findings that underlie a district court’s claim construction.” Teva Pharm. USA, Inc. v. Sandoz, Inc., — U.S.-, 135 S.Ct. 831, 841-42, — L.Ed.2d-(2015).

II. The District Court Correctly Construed “Nanoparticles” and “Microparticles”

All asserted claims require a matrix formed of, among other things, “nanoparti-cles” and “microparticles” of a taxane. See, e.g., '493 patent col. 12 1. 4. Claim 1 is representative:

A pharmaceutical composition comprising a porous matrix formed of a hydro-philic excipient, a wetting agent and nanoparbicles and microparticles of a taxane, wherein the nanoparticles and microparticles have a mean diameter between, about 0.01 and 5 p. and a total surface area greater than about [0.5 m 2 ] 0.5 to 2 /mL, wherein the porous matrix is in a dry powder form, and wherein upon exposure to an aqueous medium, the matrix dissolves to leave the taxane nanoparticles and microparticles, wherein the dissolution rate of the tax-ane nanoparticles and microparticles in an aqueous solution is increased relative to unprocessed taxane.

Id. col. 12 11. 2-12 (first emphasis added; second emphasis indicates an addition made upon reissue; brackets indicate a deletion from the original patent).

*665 The district court construed the term “nanoparticles” to mean “particles that have a mean diameter of between about 1 to 1000 nanometers and less than that of microparticles,” and construed “micropar-ticles” to mean “particles that have a diameter of between about 1 to 1000 microns and greater than that of nanoparticles.” J.A. 28-29; see also Cephalon, 985 F.Supp.2d at 175-78. The district court found these constructions supported by the “widely accepted definition” of the terms nanoparticles and microparticles. Cephal-on, 985 F.Supp.2d at 176. It also found “that other Acusphere patents in the same field, many credited to the inventors of the '493 patent,” define microparticles as ranging from 1 to 1000 microns (pm) and nano-particles as ranging from 1 to 1000 nanometers (nm). Id. The district court also looked to a textbook, entitled Microparti-culate Systems for the Delivery of Proteins and Vaccines, which further confirmed this understanding.

Acusphere first argues the “ ‘widely accepted definitionfs]’ ” of the disputed terms are “not standard usage.” Appellants’ Br. 18 (quoting Cephalon, 985 F.Supp.2d at 176). As the United States Supreme Court has recently instructed, “ ‘how the art understands] [a] term ... [is] plainly a question of fact.’ ” Teva, 135 S.Ct. at 838 (quoting Harries v. Air King Prods., Co., 183 F.2d 158, 164 (2d Cir.1950) (Hand, C.J.)). Technical words “may give rise to a factual dispute” that, “like all other factual determinations, must be reviewed for clear error.” Id. at 837-38. The terms “microparticles” and “nanopar-ticles” are technical words, and how the relevant scientific community understands them is therefore a question of fact reviewable for clear error.

Acusphere fails to establish clear error. It asserts “ ‘there is no universally agreed definition of the size of a nanoparticle.’” Appellants’ Br. 20 (emphasis modified) (quoting Cephalon, 985 F.Supp.2d at 176). However, the district court described its finding as to how the art understood the terms nanoparticles and microparticles not as “universal” but as “widely accepted.” Cephalon, 985 F.Supp.2d at 176. To the extent Acusphere is arguing the district court committed legal error by basing its construction on an understanding that was less than universally accepted, a definition need not be universally accepted to form a proper basis for claim construction. See Phillips v. AWH Corp., 415 F.3d 1303

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