Hendrix v. Novartis Pharmaceutical Corp.

975 F. Supp. 2d 1100, 2013 WL 5491846, 2013 U.S. Dist. LEXIS 143936
CourtDistrict Court, C.D. California
DecidedOctober 2, 2013
DocketCase No. CV-13-2402-MWF (PLAx)
StatusPublished
Cited by5 cases

This text of 975 F. Supp. 2d 1100 (Hendrix v. Novartis Pharmaceutical Corp.) is published on Counsel Stack Legal Research, covering District Court, C.D. California primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hendrix v. Novartis Pharmaceutical Corp., 975 F. Supp. 2d 1100, 2013 WL 5491846, 2013 U.S. Dist. LEXIS 143936 (C.D. Cal. 2013).

Opinion

ORDER GRANTING DEFENDANT NOVARTIS PHARMACEUTICALS CORPORATION’S MOTION FOR SUMMARY JUDGMENT [106]

MICHAEL W. FITZGERALD, District Judge.

This matter is before the Court on Defendant Novartis Pharmaceuticals Corporation’s (“NPC”) Motion for Summary Judgment (the “Motion”). (Docket No. 106). This case was assigned to this Court on March 19, 2013.

I. BACKGROUND

A. Undisputed Facts

Plaintiff Michel Hendrix was diagnosed with multiple myeloma in September 1999 by his oncologist, Dr. Berenson. (Plaintiffs Counter-Statement of Uncontroverted Facts (“PCUF”) ¶ 1). As part of his treatment for bone-related symptoms of his cancer, Dr. Berenson placed Plaintiff in [1103]*1103a clinic trial in September 1999, in which Plaintiff received 4mg infusions of the bisphosphonate drug Zometa every three to four weeks. (Defendant’s Statement of Uncontroverted Facts (“SUF”) ¶ 33; PCUF ¶ 3). His Zometa treatment followed this regimen until it was discontinued in October 2003. (SUF ¶ 72). Zometa was approved by the FDA in February 2002. (SUF ¶ 3).

In September 2002, Plaintiffs dentist, Dr. Powell, noticed exposed bone in his lower right jaw. (PCUF ¶ 5; SUF ¶ 49). Dr. Powell referred him to an oral surgeon, Dr. Salaita, who recommended and performed a sequestrectomy to remove Plaintiffs exposed dead bone on October 4, 2002. (PCUF ¶¶ 6, 8; SUF ¶ 50). Plaintiff continued to have exposed bone in his lower right jaw, and he consulted an endodontist who performed a root canal on tooth number 31 on November 5, 2002. (PCUF ¶ 9-10; SUF ¶ 51). This procedure was unsuccessful, and Dr. Salaita performed a series of procedures over the next three months designed to relieve Plaintiffs pain and resolve the exposed bone issue, including another sequestrectomy, an incision and drain of an infected area, and extractions of teeth 30 and 31. (PCUF ¶¶ 11-13). During the next seven months, Plaintiff underwent further treatments on his lower right jaw, including an extraction of tooth 32 and another sequestrectomy, but he continued to suffer from exposed necrotic bone. (PCUF ¶¶ 14-16; SUF ¶¶ 53-54). Dr. Salaita’s notes dated April 2, 2003, state that Plaintiffs jaw issue was “probably secondary to monthly Prednisone and Zometa (bisphosphonate).” (SUF ¶ 57). He later referred to his reference to Zometa in that note as “something of a guess.” (Salaita Dep. at 42).

Dr. Salaita referred Plaintiff to Dr. Felsenfeld, an oral and maxillofacial surgeon, in or around September 2003. (PCUF ¶ 16). Dr. Felsenfeld met with Plaintiff on September 18, 2003, and the doctor noted his impression that Plaintiff had “bisphosphonate osteonecrosis” (osteonecrosis of the jaw, or “ONJ”). (SUF ¶ 59; PCUF ¶ 17). Plaintiff testified that at his first meeting with Dr. Felsenfeld, he informed the doctor that he believed his jaw problems resulted from Zometa, although he could not remember the date of that meeting. (SUF ¶ 61; Plaintiffs Responses to Defendant’s Statement of Uncontroverted Facts (“PRSUF”) ¶ 61).

On October 14, 2003, Plaintiff saw Dr. Barstis, an oncologist who had been treating him since 1999, to discuss discontinuing Zometa treatment. (PCUF ¶ 4; SUF ¶ 69). At that meeting, Plaintiff and Dr. Barstis decided to stop the Zometa treatment. (SUF ¶ 72). Dr. Barstis had spoken to Dr. Felsenfeld regarding Dr. Felsenfeld’s clinical impressions regarding the connection between Zometa and ONJ. (SUF ¶ 69). Around the same time, Dr. Barstis also discussed the connection with Dr. Berenson. (SUF ¶ 70; PRSUF ¶ 70; Barstis Dep. at 56). On November 4, 2003, Plaintiff saw an orthopedic doctor, Dr. Bloze, who noted that “it is believed” that Plaintiffs Zometa treatments were discontinued because it caused his ONJ. (SUF ¶¶ 74-75).

In January 2007, Plaintiff resumed Zometa treatments once per year. (SUF ¶ 80). He and Dr. Barstis chose to resume the treatment on a much less frequent basis than he had taken it from 1999 to 2003 because Dr. Barstis believed that once per year treatments were “extremely unlikely” to cause ONJ. (PCUF ¶¶ 41-42, 45; Barstis Dep. at 68). His yearly Zometa regimen continues today. (SUF ¶ 81).

B. Procedural History

Plaintiff filed his Complaint against NPC in the Eastern District of New York [1104]*1104on January 13, 2006. (Docket No. 1). The case was consolidated in 2007 into multidistrict litigation (“MDL”) in the Middle District of Tennessee, along with over a dozen other cases alleging harms suffered from treatment with bisphosphonate drugs Aredia and Zometa. That multidistrict litigation was styled In re Aredia & Zometa Products Liability Litigation, No. 3:06—md-1760 (M.D. Tenn.) (“MDL 1760”). NPC filed its first iteration of the present Motion in the MDL on May 17, 2011 (Hendrix v. Novartis Pharm. Corp., No. 3:06—cv-374 (M.D.Tenn.) (“Case 06-374”), Docket No. 28), but before it could be heard the cases of the MDL were remanded to their respective districts. (Case 06-374, Docket No. 53). The parties then moved to transfer the instant action from the Eastern District of New York to this Court. (Docket No. 56).

On April 22, 2013, this Court held a preliminary Status Conference to determine the best course to proceed with litigation. (Docket No. 75). Pursuant to the Court’s order, the parties filed a Joint Status Report (“JSR”) on May 6, 2013 (Docket No. 83), in which NPC requested leave to supplement the Motion for Summary Judgment it had filed in the MDL with additional briefing to address governing Ninth Circuit law and any factual and legal developments that may have arisen in the two years since the original motion was filed. (JSR at 7). The Court issued a Scheduling Order allowing this supplemental briefing (Docket No. 84), and NPC filed the present Motion on August 16, 2013. (Docket Nos. 106-09). The present Motion includes an argument that Plaintiffs action is barred by the applicable statute of limitations, an argument that was omitted from NPC’s original Motion for Summary Judgment. Plaintiff filed an Ex Parte Application to Strike the Motion, arguing, inter alia, that the statute of limitations argument was nonsupplemental, and thus the Motion fell beyond the scope of the Court’s Scheduling Order. (Docket Nos. 117-18). The Court denied Plaintiffs application. (Docket No. 124).

II. DISCUSSION

A. Legal Standard

Under the Federal Rules of Civil Procedure, a movant is entitled to summary judgment if it can demonstrate that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law. Fed.R.Civ.P. 56(a). In deciding a motion for summary judgment under Rule 56, the Court applies Anderson, Celotex, and their Ninth Circuit progeny. Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986); Celotex Corp. v. Catrett, 477 U.S. 317, 323-24, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986).

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Bluebook (online)
975 F. Supp. 2d 1100, 2013 WL 5491846, 2013 U.S. Dist. LEXIS 143936, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hendrix-v-novartis-pharmaceutical-corp-cacd-2013.