Linda Messick v. Novartis Pharmaceuticals Corp.

747 F.3d 1193, 94 Fed. R. Serv. 153, 2014 WL 1328182, 2014 U.S. App. LEXIS 6257
CourtCourt of Appeals for the Ninth Circuit
DecidedApril 4, 2014
Docket13-15433
StatusPublished
Cited by134 cases

This text of 747 F.3d 1193 (Linda Messick v. Novartis Pharmaceuticals Corp.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Ninth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Linda Messick v. Novartis Pharmaceuticals Corp., 747 F.3d 1193, 94 Fed. R. Serv. 153, 2014 WL 1328182, 2014 U.S. App. LEXIS 6257 (9th Cir. 2014).

Opinion

OPINION

GOULD, Circuit Judge:

We consider when a district court should exclude expert testimony at trial. Linda Messick contends that the district court erred by excluding the causation testimony offered by her expert, Dr. Richard Jackson, when it found the testimony to be irrelevant and unreliable. Examining, the district court’s exclusion of expert testimony for an abuse of discretion, we conclude that Dr. Jackson’s testimony was improperly excluded, and we reverse and remand.

I

In August 2000, Linda Messick was diagnosed with breast cancer. In response to her development of osteoporosis after chemotherapy and steroid therapy, Mes-sick was treated with the drug Zometa from May 7, 2002 to November 14, 2002. Zometa is a bisphosphonate, a class of drug commonly used to treat multiple myeloma. Such drugs are used to reduce or eliminate the possibility of skeletal-related degeneration and injuries to which cancer patients are particularly susceptible. Novartis Pharmaceuticals Corporation (“Novartis”) produces Zometa, which was approved by the FDA in 2001 and 2002 for treating hypercalcemia of malignancy and other conditions.

After Messick encountered several dental problems, two oral specialists examined her in November 2005 and discovered os-teonecrosis near three of her teeth. Both doctors treated her under the assumption that she was suffering from bisphospho-nate-related osteonecrosis of the jaw (“BRONJ”), a condition recognized by the American Association of Oral and Maxillo-facial Surgeons (“AAOMS”). According to the AAOMS, a BRONJ diagnosis is appropriate for patients with (1) current or previous treatment with bisphosphonates, (2) exposed bone in the maxillofacial region that has lasted for more than eight weeks, and (3) no history of radiation therapy to the jaw. Other potential causes of osteo-necrosis of the jaw (“ONJ”) may include: peridontal and dental disease, osteomyeli-tis, corticosteroid use, cancer, radiation therapy, compromised immunity, and trau *1196 ma. While ONJ may be caused by many factors, the AAOMS’s diagnostic definition of BRONJ sets out its unique features: it lasts more than eight weeks and is not related to radiation therapy. Messick’s BRONJ healed between March and October 2008, about three years after diagnosis. She and her husband brought suit against Novartis for strict products liability, negligent manufacture, negligent failure to warn, breach of express and implied warranty, and loss of consortium.

To support her claims, Messick offered Dr. Jackson’s testimony on ONJ and BRONJ generally, and on the causal link between her bisphosphonate treatment and later development of BRONJ. Dr. Jackson graduated from the University of the Pacific’s School of Dentistry in 1974, completed his oral and maxillofacial surgery residency in 1982, and became Board Certified in oral maxillofacial surgery in 1984. He belongs to several dental and oral maxillofacial professional groups, and has published and lectured on a variety of topics over many years. Dr. Jackson has extensive experience diagnosing and treating ONJ, including ONJ in patients who had been treated with bisphosphonates, and he is the primary oral and maxillofa-cial surgeon managing ONJ in the Sacramento area.

While the action was pending in Multi-District Litigation proceedings, Novartis filed a motion to exclude the specific causation testimony of Messick’s experts and a motion seeking summary judgment. After the case was remanded and transferred, the district court granted those motions, and Messick appeals the exclusion of Dr. Jackson’s causation testimony and the ensuing grant of summary judgment to Novartis.

II

We review a ruling on the admissibility of expert testimony for an abuse of discretion, Primiano v. Cook, 598 F.3d 558, 563 (9th Cir.2010), but review de novo the “construction or interpretation of ... the Federal Rules of Evidence, including whether particular evidence falls within the scope of a given rule.” United States v. Durham, 464 F.3d 976, 981 (9th Cir.2006) (citations omitted).

The substantive issue here arises under the Federal Rules of Evidence and California state products liability law. Federal Rule of Evidence 702 governs expert testimony:

A witness who is qualified as an expert by knowledge, skill, experience, training, or education may testify in the form of an opinion or otherwise if:
(a) the expert’s scientific, technical, or other specialized knowledge will help the trier of fact to understand the evidence or to determine a fact in issue;
(b) the testimony is based on sufficient facts or data;
(c) the testimony is the product of reliable principles and methods; and
(d) the expert has reliably applied the principles and methods to the facts of the case.

Fed.R.Evid. 702. Although Rule 702 should be applied with a “liberal thrust” favoring admission, Daubert v. Merrell Dow Pharm., Inc., 509 U.S. 579, 588, 113 S.Ct. 2786, 125 L.Ed.2d 469 (1993), it requires that “[ejxpert testimony ... be both relevant and reliable,” Estate of Barabin v. AstenJohnson, Inc., 740 F.3d 457, 463 (9th Cir.2014) (alteration and omission in original) (quoting United States v. Vallejo, 237 F.3d 1008, 1019 (9th Cir.2001)).

The relevancy bar is low, demanding only that the evidence “logically advances a material aspect of the proposing party’s case.” Daubert v. Merrell Dow Pharm., Inc., 43 F.3d 1311, 1315 (9th Cir.1995) (“Daubert II ”). Relevancy depends *1197 on the particular law at issue because “[ejxpert opinion testimony is relevant if the knowledge underlying it has a valid connection to the pertinent inquiry.” Primiano, 598 F.3d at 565. Here, California state products liability law requires only that a plaintiff show that the defendant’s conduct was “more likely than not” a substantial factor in causing the injury in order to prove specific causation. See Saelzler v. Advanced Grp. 400, 25 Cal.4th 763, 107 Cal.Rptr.2d 617, 23 P.3d 1143, 1152 (2001).

The district court excluded Dr. Jackson’s testimony as irrelevant because of its view that his “differential diagnosis only determines that Ms. Messick’s ONJ is related

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747 F.3d 1193, 94 Fed. R. Serv. 153, 2014 WL 1328182, 2014 U.S. App. LEXIS 6257, Counsel Stack Legal Research, https://law.counselstack.com/opinion/linda-messick-v-novartis-pharmaceuticals-corp-ca9-2014.