Amgen Inc. v. F. Hoffmann-LaRoche LTD et al
Filing
721
MOTION for Leave to File Sur-Reply in Support of Opposition to Amgen's Motion for Summary Judgment of Infringement of '422 Claim 1, '933 Claim 3, and '698 Claim 6 by F. Hoffmann-LaRoche LTD, Roche Diagnostics GmbH, Hoffmann LaRoche Inc.. (Attachments: #1 Exhibit Defendants' Surreply in Support of Opposition to Amgen's Motion for Summary Judgment of Infringement of '422 Claim 1, '933 Claim 3, and '698 Claim 6#2 Affidavit Declaration of Keith E. Toms in Support of Defendants' Surreply#3 Exhibit Exhibit A to Toms Declaration#4 Exhibit Exhibit B to Toms Declaration#5 Exhibit Exhibit C to Toms Declaration)(Toms, Keith)
Amgen Inc. v. F. Hoffmann-LaRoche LTD et al
Doc. 721 Att. 5
Case 1:05-cv-12237-WGY
7/3/2007 Lodlsh. Harvey
Document 721-6
Filed 07/13/2007
7/3/2007 Lodi.h. Harvey
Page 1 of 2
1 2
Exhibits: 1-21 Volume 1, Pages 1-306
UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MASSACHUSETTS
Ci vil Action No. 05 Ci v. 12237 WGY
1
INDEX
EXANATIONS
2 3
4
3
4
5
AMEN INC.
6
HAVEY F. LODISH, Ph.D.
BY MS. BEN-AMI
7
Plaintiff
vs.
F. HOFF-LA ROCHE LTD.,
5 6 7 8
9
7 8
9
BY MR. DAY
282 296
BY MS. BEN-AM
ROCHE DIAGNOSTICS GmH, and
10
10
EXHIBITS MAD
Exhibi t 1 Expert Report of Harvey F.
6
HOFF-LA ROCllE INC.
11 12 13
VIDEOTAPED DEPOSITION OF
14
11 12 13
Defendants
Lodish, Ph.D. Regarding Infringement
Exhibi t 2 Rebuttal Expert Report of
Harvey F. Lodish, Ph.D.
6
15 16
17
Tuesday ¡ July 3, 2007, 9: 04 a. m.
Duane Morris LLP 470 Atlantic Avenue Boston, Massachusetts
HAVEY F. LODISH, Ph.D.
14
15
16 17
Exhibit 3 Supplemental Expert Report
of Harvey F. Lodishi Ph.D.
6
Exhibit 4 Third Supplemental Expert
Report of Harvey F. Lodish, Ph.D.
6
18
19
.. TRASCRIPT DESIGNATED CONFIDENTIAL OUTSDIE ATTORNY'S Eis" S C.,..
FAR ARSENAULT BROCK LLC
20 21 22 23
24
19
Exhibit 5 Claim Construction Chart
6 6 6 6 6
Reporting For:
20
21
Exhibi t 6 U. S. Patent 5,955,422
Exhibit 7 U.S. Patent 5,618.698
LiveNote World Service 221 Main Street, Suite 1250 San Francisco, California 94105 Phone: 415-321-2300
22
23
24
Exhibi t 8 U. S. Patent 4,703,008
Exhibit 9 U.S. Patent 5,756,349
Fax: 414-321-2301
Reported by:
JANIS T. YOUNG, RDR, CRR
25
(Continued)
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713/2007 Lodlsh. Harvey
7/31007 Lodl$h. Harvey
1
APPEACES:
Lloyd R. Day, Jr., Esq.
1
Exhibit 10 U.S. Patent 5,441,868
2 3
4
2 3
Exhibi t 11 U. S. Patent 5,621,080
Exhibit 12 U.S. Patent 5,547,933
6 6
Day Casebeer Madrid & Batchelder LLP
20300 Stevens Creek Boulevard
Cupertino i California 95014
5
6 7
Exhibi t 13 Second Supplemntal Expert
Report of Harvey F. Lodish, Ph.D.
48
5
6 7
408.873.0110 fax: 408.873.0220
irdayßdaycasebeer. com
Exhibit 14 Excerpt from Textbook,
48
Molecular Cell Biology, Sixth
8
9
for Plaintiff
8
9
Edition, by Lodish, et al.
Exhibit 15 Color Pictures from
Attachments to Jorgensen Report
179 200
10 11
12
Leora Ben-~ i Esq.
Graham Pechenik, Esq.
Danielle Noonan i Esq.
10 11
Exhibit 16 Application for United
States Letters Patent, with Cover Sheet dated 12-13-83, AM-ITC
12
13
13
14
Kaye Scholer LLP
425 Park Avenue, 12th Floor New York, New York 10022-3598
14
00948379-00948649
Exhibit 17 Application for United
States Letters Patent, AM-ITC
15
16 17 18 19
15
16 17 18
200
212.836.8000 fax: 212.836.8689
lbenamekayescholer. com
gpechenikGkayescholer. com
dnoonanGkayescholer. com
00470468-00470531
Exhibit 18 Application for United
States Letters Patent, AM-ITC
200
19 20
21
20
21 22
for Defendants
00470717-00470813
Exhibit 19 Application for United
States Letters Patent, AM-ITC
200
ALSO PRESENT:
Adam Cook i videographer
22 23
24
23
24
00869737-00869844
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(Continued)
Dockets.Justia.com
Case 1:05-cv-12237-WGY
7/3/2007 Lodish, Harvey
Document 721-6
Filed 07/13/2007
1/312007 Lodi5h, Harvey
Page 2 of 2
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Q. Why is the binding affinity of CERA
different than EPO?
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A. The binding affinity of CERA to the EPO
receptor different from the binding affinity of EPO?
r don't think it is known why. I can offer you one
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explanation.
Q. SO the answer is l it i S not known why, but
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713/2007 Lodi.h, Harvey
7131007 Lodi.h, Harvey
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you have a hypothesis?
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A. I have several hypotheses. I will offer
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you one.
Q. Can you offer them all to me?
A. Well, let's go through one at a time.
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Q. Okay.
A. ThG first hypothesis is l CERA is a mixture
of 90 percent dead protein and 10 percent functional
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protein. That is, the simplest exlanation of what
happens after PEGylation is, you kill, in some unknown way, roughly 90 percent of the EPO
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molecules. They're dQad.
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