`
`BMS-201038
`
`Indication:
`
`Hyperlipidemia
`
`Protocol No.:
`
`CVl45-009
`
`Phase:
`
`I
`
`Study Initiation Date:
`
`19-Feb-1999
`
`Study Completion Date:
`
`22-Dec-1999
`
`Report Date:
`
`07-Jan-2002
`
`THE EFFECTS OF CHRONIC DOSING OF BMS-201038 ON HEPATIC FAT
`
`ACCUMULATION AND REVERSIBILITY AS ASSESSED BY NUCLEAR
`
`MAGNETIC RESONANCE SPECTROSCOPY (NMRS)
`
`AN ABBREVIATED CLINICAL STUDY REPORT
`
`
`
`
`
`
`This document is a confidential communication of Bristol-Myers Squibb Company. Acceptance of this
`document constitutes an agreement by the recipient that no unpublished information contained herein will
`be published or disclosed without Bristol-Myers Squibb Company's prior written approval. except that this
`
`document may be disclosed to appropriate Institutional Review Committees so long as they are requested to
`
`kee it confidential. This study was conducted in accordance with Good Clinical Practice.
`
`
`
`Name and Affiliation of Principal Investigators:
`'
`William Insull, MD. (Houston), Carlos Dujovne, M.D.(Kansas), Howard Knapp, M.D.,
`Ph.D.(University of Iowa), Daniel Radcr, M.D.(University of Pennsylvania), Evan Stein,
`M.D., Ph.D. (Cincinnati)
`
`Company Signatory
`Richard A. Reeves, M.D.
`Bristol-Myers Squibb
`Princeton, NJ 08543-4000
`Tel: 609-252-3452
`
`Fax: 609-252-6313
`
`Department of Clinical Discovery
`Drug Discovery and Exploratory Development
`Bristol-Myers Squibb Pharmaceutical Research Institute
`Bristol-Myers Squibb Company
`Bristol-Myers Squibb
`Princeton, NJ 08543-4000
`
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`IDIS:930UU110J—V1.0.C-V1.0
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`CV14 5-00°
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`BMS-20l03S
`Abbreviated Clinical Study Report
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`FINAL REPORT SYNOPSIS
`
`INTRODUCTION: BMS-201038 is an inhibitor of microsomal triglyceride transfer protein (MTP). In
`studies conducted in human volunteers BMS-201038 was shown to be a potent agent for lowering LDL~C
`and uiglycerides. As an inhibitor of MTP it has the potential to increase hepatic fat content. To assess the
`possible accumulation of hepatic fat, 3 nuclear magnetic resonance spectroscopy (NMRS) technique was
`developed. This technique was originally described as a method to assess fat content in bone marrow, and
`subsequently developed as part of the MT? program to determine percent fat
`in the liver. In Protocol
`CVl45-002. this technique demonstrated that at all doses of BMS—201038 from l0 mg QD to 100 mg QD.
`there appeared to be an increase in hepatic fat content. To further define the safety of this compound. a
`Reversibility Protocol, CV145-009. was developed to assess the extent of any hepatic fat accumulation and
`the degree of reversibility at 6 weeks post dosing of any accumulated hepatic faL Based on the results of
`this trial, further clinical development on BMS-201038 was discontinued due to safety eoncems. Therefore
`an Abbreviated Study Report is being issued.
`
`TITLE OF STUDY:
`
`INVEST] GATORS:
`
`The Effects of Chronic Dosing of BMS-201038 on Hepatic I-‘at Accumulation
`and Reversibility as Assessed by Nuclear Magnetic Resonance Spectroscopy
`TNMRS)
`
`Study conducted at 5 study centers in the USA. The Principal investigators
`(site number) were William lnsull, M.D. (001), Carlos Dujovne. M.D. (002).
`Howard Knapp, M.D.. Ph.D. (003), Daniel Radar, M.D. (007), Evan Stein,
`M.D., Ph.D. (008)
`
`STUDY CENTERS:
`
`001: Lipid Research Clinic. Baylor College of Medicine, Houston. TX
`
`002: Mid-Continent Clinical Trials, Overland, KS
`
`003: Lipid Research Clinic, Iowa City, IA
`
`004: Hospital of the University of Pennsylvania, Philadelphia, PA
`
`008: Metabolic and Atherosclerosis Research Center, Cincinnati. OH
`None
`
`Date first subject enrolled:
`
`I9-Feb-I999
`
`Date last subject completed: 22-Dec-1999
`I
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`PUBLICATIONS:
`
`STUDY PERIOD:
`
`
`
`CLINICAL PHASE:
`
`
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