Education and Honors

  • J.D., University of Kansas School of Law, 1981
    Order of the Coif
    Member, Kansas Law Review
  • B.S., journalism, University of Kansas, 1978
  • Defense Research Institute, Exceptional Performance Citation, 1995

    International Who's Who of Product Liability Defense Attorneys, published by Law Business Research Ltd., every year since 2001

    International Who's Who of Life Sciences Attorneys, 2010 and 2011

    Texas Super Lawyer, 2006 and 2008 - 2011

    Chambers USA, 2007 - 2011

    Who's Who Legal: Texas, 2008

Admissions/Affiliations

State Bar of Texas

Missouri Bar

United States Courts of Appeal for the Fourth, Fifth, Sixth, Seventh, Eighth, Ninth and Tenth Circuits

United States District Courts for the Northern, Southern, Eastern and Western Districts of Texas, the District of Colorado and the Eastern and Western Districts of Missouri

United States Supreme Court

IADC CLE Board, Chair, 2005-2006

IADC Pharmaceutical, Medical Device and Biotechnology Committee, Chair, 2000

IADC Trial Academy, Faculty, 1998

Missouri Organization of Defense Lawyers, President, 1994 to 1995

One Shell Plaza
910 Louisiana Street
Houston, Texas 77002-4995
United States
Phone:
+1.713.229.1659
Fax:
+1.713.229.2859

Concentration

Pharmaceutical and medical device litigation, including products liability, toxic tort, commercial and patent litigation

Summary

Steve Scheve's emphasis over the past 30 years has been in the pharmaceutical, medical device and chemical industries. Mr. Scheve has defended and tried cases throughout the country and has acted as national coordinating counsel for clients in multiple litigations, each involving lawsuits in over thirty states. In addition to his trial work, he has successfully argued appeals on issues of importance to manufacturers in multiple appellate courts.

Mr. Scheve has handled numerous commercial disputes for pharmaceutical clients involving patents, royalty, supply, license, co-promotion, development and interference settlement agreements. These disputes have included several arbitrations, with controversies involving as much as $1 billion.

Mr. Scheve has acted as national counsel in litigations involving five prescription drugs. He has acted as regional counsel in multiple other litigations. He has handled/supervised over 600 prescription drug cases and was the designated trial lawyer for a major tobacco manufacturer in smoking and health cases in Texas, Mississippi, Alabama, Arkansas, Oklahoma and New Mexico.

In each of the past ten years, Mr. Scheve has been identified by the International Who's Who of Product Liability Defense Lawyers as one of the "best." He successfully argued against the adoption of market share liability in the Illinois Supreme Court in Smith v. Eli Lilly and Company, et al. He also successfully argued for application of comment k of §402A as a matter of law to all FDA-approved prescription drugs in the Utah Supreme Court in Grundberg v. The Upjohn Company.

Representative Engagements

Practice Overview

  • 18 pharmaceutical companies – litigation in hundreds of cases involving anxiolytics, chemotherapeutic agents, hypnotics, benzodiazepines, injectable corticosteroids, hormone replacement therapies, blood products, pain relief medications, contrast media, cold remedies, anti-angina drugs, pulmonary hypertension drugs, anesthesia drugs, antibiotics, monoclonal antibodies, surgical devices and HIV test kits

Pharmaceutical Trial Experience

  • McMahon v. Eli Lilly and Company, N.D. Illinois (1984)  Directed verdict in DES trial involving claim of adenosis and other non-cancerous injuries to reproductive tract of DES daughter
  • Bogorad v. Eli Lilly and Company, E.D. Michigan (1986) Directed verdict in DES case involving claim of adenosis and other non-cancerous injuries to reproductive tract of DES daughter
  • Harley v. The Upjohn Company, Bexar County, Texas (1992) Defense verdict after two previous mistrials; claims of aberrant behavior and personal injury stemming from use of triazolobenzodiazepine sleeping pill (Halcion®)
  • Freeman v. The Upjohn Company, Dallas County, Texas (1994) Jury verdict of $200,000 reversed and rendered in favor of defendant in Halcion® case involving claims of aberrant behavior/psychosis after high-dosage use of triazolobenzodiazepine sleeping pill
  • Williams v. The Upjohn Company, S.D. Texas (1996) Defense verdict in Halcion® case involving claims of aberrant behavior stemming from long-term use of triazolobenzodiazepine sleeping pill
  • Solvay Pharmaceuticals, Inc. v. The Upjohn Company Three-week evidentiary hearing before three-judge arbitral panel in Atlanta, Georgia (1999) $150 million dispute over alleged breach of co-promotion agreement relating to a selective serotonin reuptake inhibitor (Luvox®) and a selective norepinephrine reuptake inhibitor (reboxetine); favorable outcome for client in which no money changed hands
  • NeoPharm v. Pharmacia and Upjohn Company Four-month evidentiary hearing before three-judge arbitral panel in Washington, D.C. (2003-2004) $1 billion dispute over alleged breach of license agreement relating to chemotherapy agents (paclitaxel and doxorubicin); panel awarded plaintiff zero damages
  • Elan v. King Pharmaceuticals (2006) Two-week evidentiary hearing before three-judge arbitral panel in New York City involving breach of a license and development agreement; favorable outcome for client with a $50 million award
  • Elan v. Abraxis Bioscience (2008) Two week jury trial involving patent infringement, invalidity and unenforceability claims. Jury found in favor of client, finding patents to be valid and enforceable. Jury also found infringement and awarded client $55.2 million in damages
  • Asahi Kasei Pharma v. CoTherix (2009) Two week trial before three judge arbitration panel in San Francisco involving breach of license agreement. Panel awarded plaintiff $68 million