Sofregen Medical Inc. v. Allergan Sales, LLC ( 2023 )


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  •              IN THE SUPERIOR COURT OF THE STATE OF DELAWARE
    SOFREGEN MEDICAL INC., a Delaware             )
    Corporation; and SOFREGEN MEDICAL             )
    IRELAND LIMITED, an Irish Private             )
    Limited Company,                              )
    )
    Plaintiffs/Counterclaim-        )
    Defendants,                     )
    )
    v.                                     )
    )    C.A. No.: N20C-03-319 EMD CCLD
    ALLERGAN SALES, LLC, a Delaware               )
    Limited Liability Company; and                )
    ALLERGAN PHARMACEUTICALS                      )
    HOLDINGS (IRELAND), an Irish                  )
    Incorporated Private Unlimited Liability      )
    Company,                                      )
    )
    Defendants/Counterclaim-        )
    Plaintiffs.                     )
    Upon Defendant/Counterclaim-Plaintiffs’ Motion to
    Exclude Dr. Kaufman’s Expert Reports and Testimony
    DENIED
    Brian M. Rostocki, Esquire, Benjamin P. Chapple, Esquire, Anne M. Steadman, Esquire, Reed
    Smith LLP, Wilmington, Delaware. Attorneys for Defendants/Counterclaim-Plaintiffs Allergan
    Sales, LLC and Allergan Pharmaceuticals Holdings (Ireland).
    Thomas A. Uebler, Esquire, Kathleen A. Murphy, Esquire, Adam J. Waskie, McCollom
    D’Emilio Smith Uebler LLC, Wilmington, Delaware. Attorneys for Plaintiffs/Counterclaim-
    Defendants Sofregen Medical Inc. and Sofregen Medical Ireland Limited.
    DAVIS, J.
    I.        INTRODUCTION
    This is a breach of contract and fraudulent inducement action assigned to the Complex
    Commercial Litigation Division of this Court. In November 2016, Plaintiffs Sofregen Medical
    Inc. and Sofregen Medical Ireland Limited (collectively, “Sofregen”) purchased from Allergan
    Sales, LLC and Allergan Pharmaceuticals Holdings (Ireland) (collectively, “Allergan”) certain
    “silk biomaterial surgical mesh” (“SERI”) products for use in reconstructive surgeries.1 The
    purchase occurred via an asset purchase agreement (the “APA”) between Sofregen and
    Allergan.2
    II.     THE MOTION IN LIMINE
    Allergan seeks to exclude the expert reports and testimony of Dr. Jedediah Kaufman. Dr.
    Kaufman is a practicing general surgeon “that evaluates clinical trial data to determine which
    medical devices to employ in his practice.”3 Dr. Kaufman also reviews safety profiles and costs
    of medical devices in advising hospitals on which products should be purchased and used.4
    Sofregen retained Dr. Kaufman as an expert witness to opine on the materiality of the SURE-002
    study, SURE-006 study, among other relevant studies.5 It appears Dr. Kaufman’s expert
    opinions touch on how a prospective purchaser (a clinician) of SERI would view the product, as
    well as the reasonableness of Sofregen’s reliance on Allergan’s pre-closing representations
    regarding SERI.6 These issues were front and center in the Court’s Summary Judgment Opinion,
    and the Court cited Dr. Kaufman’s expert reports multiple times in that opinion.7
    Allergan makes four arguments to exclude Dr. Kaufman’s expert reports and testimony:
    (i) Dr. Kaufman misunderstands the nature of expert opinions; (ii) Dr. Kaufman is not qualified
    because he lacks the requisite knowledge, skill, experience, training, or education; (iii) several of
    Dr. Kaufman’s opinions should be excluded because they are not supported by sufficient facts or
    1
    Second Amended Complaint (“Second Am. Compl.”) ¶ 1. D.I. No. 20.
    2
    Id.
    3
    D.I. 186 at 2.
    4
    Id.
    5
    Id. at 3-4.
    6
    Id. at 4.
    7
    See D.I. 182 at 4, 7, 18.
    1
    data; and (iv) Dr. Kaufman’s “non-expert opinions” should be excluded because they are
    inadmissible “common sense opinions.”8
    Sofregen responds with five points: (i) Dr. Kaufman is a qualified expert because he is a
    surgeon opining on the significance of clinical trial data authored by medical doctors about a
    surgical mesh used by surgeons; (ii) Dr. Kaufman is not offering opinions on topics outside his
    scope of expertise, such as FDA and regulatory guidelines and procedures; (iii) Dr. Kaufman’s
    opinions are supported by sufficient facts and data; (iv) Dr. Kaufman is not providing any “non-
    expert opinions”; and (v) Dr. Kaufman’s opinions will assist the trier of fact, i.e., the Court.9
    Sofregen contends that most of Allergan’s arguments go to credibility, not admissibility.10
    The Court agrees with Sofregen’s arguments and will DENY Allergan’s motion to
    exclude Dr. Kaufman.
    III.     LEGAL STANDARD
    Delaware Rule of Evidence 702 governs the admission of 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
    upon sufficient facts or data; (c) the testimony is the product of reliable principles
    and methods; and (d) the witness has applied the principles and methods reliably to
    the facts of the case.11
    D.R.E. 702 is substantially similar to F.R.E. 702.12 F.R.E. 702 was interpreted and
    further explained in Daubert v. Merrell Dow Pharmaceuticals, Inc.,13 and Kumho Tire Co., Ltd. v.
    8
    See D.I. 181 at 3-10.
    9
    See D.I. 186 at 4-11.
    10
    Id. at 7-8.
    11
    D.R.E. 702.
    12
    Bowen v. E.I. DuPont de Nemours & Co., Inc., 
    906 A.2d 787
    , 794 (Del. 2006).
    13
    
    509 U.S. 579
     (1993).
    2
    Carmichael.14 Delaware courts have adopted the holdings in Daubert and Carmichael.15 A trial
    judge must ensure an expert’s testimony is both relevant and reliable when its admission is
    challenged.16 Delaware requires the gatekeeping judge to engage in a five-step analysis to
    determine the admissibility of proffered expert testimony.17 The Court must ensure that:
    (1) the witness is qualified as an expert by knowledge, skill, experience, training,
    or education; (2) the evidence is relevant; (3) the expert’s opinion is based on
    information reasonably relied upon by experts in the particular field; (4) the expert
    testimony will assist the trier of fact to understand the evidence or to determine a
    fact in issue; and (5) the expert testimony will not create unfair prejudice or confuse
    or mislead the jury.18
    The party seeking to introduce the expert testimony carries the burden of establishing its
    admissibility by a preponderance of the evidence.19 A “‘strong preference exists’ for admitting
    expert opinions ‘when they will assist the trier of fact in understanding the relevant facts or the
    evidence.’”20
    IV.      DISCUSSION
    Allergan’s first basis to exclude Dr. Kaufman—that Dr. Kaufman misunderstands the
    nature of expert opinions—fails. After review of the relevant arguments and exhibits, the Court
    finds that Dr. Kaufman properly understands the role of expert testimony and rendering expert
    opinions.
    Allergan’s second basis—Dr. Kaufman is not qualified because he lacks the requisite
    knowledge, skill, experience, training, or education—fails. Dr. Kaufman is a practicing general
    surgeon, and he is opining on the significance of clinical trial data. Dr. Kaufman also advises
    14
    
    526 U.S. 137
     (1993).
    15
    Bowen, 
    906 A.2d at
    794 (citing M.G. Bancorporation, Inc. v. LeBeau, 
    737 A.2d 513
    , 522 (Del. 1999)).
    16
    Daubert, 
    509 U.S. at 597
    .
    17
    Bowen, 
    906 A.2d at 795
    .
    18
    
    Id.
    19
    
    Id.
    20
    Delaware ex rel. French v. Card Complaint, LLC, 
    2018 WL 4151288
    , at *2 (Del. Super. Ct. Aug. 29, 2018) (quoting
    Norman v. All About Women, P.A., 
    193 A.3d 726
    , 730 (Del. 2018)).
    3
    hospitals on which medical devices, such as surgical mesh, to purchase.21 Dr. Kaufman testified
    that he makes recommendations based on “finances” and “safety profiles” in his advisory role,
    and he acts more as a business advisor than a physician.22 Dr. Kaufman is opining on, among
    other topics, the SURE studies and the reasonableness of Sofregen’s reliance on Allergan’s pre-
    closing representations regarding SERI. The cases Allergan cites as support are inapposite.23
    Dr. Kaufman is sufficiently qualified.
    Allergan’s third basis—that several of Dr. Kaufman opinions should be excluded because
    they are not supported by sufficient facts or data—is unpersuasive. Allergan first argues Dr.
    Kaufman’s opinions regarding the reasonableness of Sofregen’s reliance on Allergan’s pre-
    closing representations are not based upon “any specific pre-closing representations.”24 Allergan
    next argues Dr. Kaufman also lacks sufficient facts or data to opine about whether the SURE
    studies had a negative impact on the market for SERI.25 Sofregen responds that Dr. Kaufman
    relied on his training and experience as a surgeon to evaluate SERI.26 Sofregen maintains Dr.
    Kaufman also independently reviewed the SURE studies and the email exhibits in this case to
    form his opinions on the reliability of SERI and Allergan’s representations.27
    21
    See D.I. 186 at 5.
    22
    
    Id.
    23
    See Goodridge v. Hyster Co., 
    845 A.2d 498
    , 503-04 (Del. 2004) (affirming a trial court ruling that granted a motion
    in limine to exclude an expert because the case was about a person injured by a forklift and the expert was not qualified
    to opine on proper forklift design safety because the expert had no experience in engineering or design safety, and
    because the expert never conducted any studies or even operated a forklift); Specter v. Texas Turbine Conversions,
    Inc., 
    2020 WL 7234363
    , at *4-5 (D. Alaska Dec. 8, 2020) (finding Dr. Kaufman in that case was not qualified to opine
    on the long-term effects of brain injuries or mental/emotional states because he is a general surgeon; but also finding
    Dr. Kaufman was “sufficiently qualified” to opine on the injured plaintiff’s injuries and cause of death). Here, Dr.
    Kaufman is opining on clinical data and representations Sofregen relied upon. The federal district court for the District
    of Alaska noted Dr. Kaufman was a surgeon “with over twenty years of training and employment in the medical field.”
    Specter, 
    2020 WL 7234363
    , at *4.
    24
    D.I. 181 at 6-7.
    25
    Id. at 7.
    26
    D.I. 186 at 8.
    27
    Id. at 9.
    4
    Generally, “the factual basis of an expert opinion goes to the credibility of the testimony,
    not the admissibility, and it is for the opposing party to challenge the factual basis of the expert
    opinion on cross-examination.”28 But when “the expert’s opinion is not based upon an
    understanding of the fundamental facts of the case, . . . it can provide no assistance to the [trier of
    fact] and such testimony must be excluded.”29
    Allergan contends that Dr. Kaufman’s opinions are “not based upon an understanding of
    the fundamental facts” of this case. But that is not true. Dr. Kaufman reviewed the SURE
    studies, among other relevant scientific papers, and reviewed the communications between
    Sofregen and Allergan. If anything, this seems more like a challenge to the factual basis of Dr.
    Kaufman’s opinions, rather than Dr. Kaufman’s lack of understanding the fundamental facts. In
    such a situation, the Court will not exclude the expert. Instead, Allergan must draw those issues
    out on cross-examination.30
    Allergan’s final basis—that Dr. Kaufman’s “non-expert opinions” should be excluded
    because they are inadmissible “common sense opinions”—is without merit. Allergan argues Dr.
    Kaufman opined about “matters concerning the FDA approval of SERI,” and that those opinions
    should be excluded because they are “common sense” and “empt[y].”31 Sofregen counters that
    Dr. Kaufman did not opine on the FDA regulatory process, but rather on Sofregen’s expectations
    of obtaining FDA approval in light of the SURE-001 study before the negative SURE-002 and -
    006 studies were revealed.32 Sofregen frames this as a “medical ethics” issue instead of a
    “regulatory process” issue.33
    28
    Perry v. Berkley, 
    996 A.2d 1262
    , 1271 (Del. 2010) (citing Porter v. Turner, 
    954 A.2d 308
    , 313 (Del. 2008)).
    29
    
    Id.
    30
    See 
    id.
    31
    D.I. 181 at 10.
    32
    D.I. 186 at 10.
    33
    
    Id.
    5
    D.R.E. 702 states in relevant part that an expert witness may testify “if scientific,
    technical, or other specialized knowledge will assist the trier of fact to understand the evidence
    or to determine a fact in issue.”34 This is sometimes called the “relevancy requirement.”35 Part
    of this inquiry includes the “distinction between testimony which is ‘common sense,’ and that
    which provides additional understanding of the issues of fact confronting the jury.”36 Delaware
    courts hold that if the jury is “equally competent to form an opinion about the ultimate fact issues
    or the expert’s testimony is within the common knowledge of the jury,” then the trial court
    should exclude the expert’s testimony.37
    The opinions that Dr. Kaufman sets forth are not “common sense.” Dr. Kaufman opines
    on, inter alia, the reasonableness of Sofregen’s expectations of getting FDA approval for SERI
    based on the results of the SURE-001 study. Dr. Kaufman further opines on the effect of the
    revelation of the SURE-002 and -006 studies and how those studies could affect gaining FDA
    approval for SERI. This is not like Knott v. Covert, where an expert’s opinion was excluded as
    “common sense” where the expert intended to opine on “the position of a scuff mark” on a
    vehicle in an auto accident case.38 The case on which Knott relies, Spencer v. Wal-Mart Stores
    East, LP, is also distinguishable. There, the trial court excluded an expert who intended to opine
    on the safety code for clearing parking lots with respect to whether Wal-Mart was negligent in
    failing to clear its lot after a snowstorm.39 The trial court did not permit the expert to testify
    34
    D.R.E. 702.
    35
    See, e.g., Knott v. Covert, 
    2015 WL 196730
    , at *2 (Del. Super. Jan. 15, 2015) (citing In re Asbestos Litig., 
    911 A.2d 1176
    , 1199 (Del. Super. 2006)).
    36
    
    Id.
     (quoting Spencer v. Wal-Mart Stores East, LP, 
    930 A.2d 881
    , 889-90 (Del. 2007)).
    37
    
    Id.
     (citing Spencer, 
    930 A.2d at 890
    ).
    38
    See id. at *3.
    39
    See Spencer, 
    930 A.2d at 889-90
    .
    6
    because the issue was “common sense” when viewing the applicable safety code in light of the
    facts.40 The Supreme Court affirmed.41 The situation in our case is much different.
    V.       CONCLUSION
    The Court will “consider [Dr. Kaufman’s] testimon[ies] in connection with the purposes
    for which it [will be] offered and in light of any flaws in the testimony that may [be] exposed
    through cross-examination.”42 Therefore, Allergan’s motion to exclude Dr. Kaufman is
    DENIED.
    IT IS SO ORDERED.
    May 25, 2023
    Wilmington, Delaware
    /s/ Eric M. Davis
    Eric M. Davis, Judge
    40
    See 
    id.
    41
    See 
    id. at 990
    .
    42
    See Beard Rsch., Inc. v. Kates, 
    8 A.3d 573
    , 593 (Del. Ch. 2010); see also 
    id.
     at 593 n.122 (citing Trs. Of Chi.
    Painters & Decorators Pension, Health & Welfare, & Deferred Sav. Plan Trust Funds v. Royal Int’l Drywall &
    Decorating, Inc., 
    493 F.3d 782
    , 788 (7th Cir. 2007) (noting that there is less of a basis to use Daubert to exclude
    testimony entirely in a bench trial because the judge can consider any shortcomings in the expert’s testimony that are
    drawn out through cross-examination)).
    7