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Reportlinker Adds Global Anti-CD20 Monoclonal Antibodies Industry
Date:10/4/2010

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Rising Number of MAbs Under Clinical Trials II-30

High Costs Impede MAbs Penetration II-30

Opportunities in Technology Development II-31

Advancements & Challenges in Antibody Production Processes II-31

Increasing Demand for Protein A in MAb Manufacturing II-32

6. RECENT DRUG APPROVALS AND REGULATORY STATUS II-33

RITUXAN RECEIVES FDA APPROVAL FOR THE TREATMENT OF Chronic

Lymphocytic Leukemia II-33

GSK Receives Positive Opinion for Arzerra™ from EMEA II-33

LFB Obtains Orphan Drug Status for LFB-R603 in Europe II-34

FDA Grants Accelerated Approval for GSK and Genmab's

Ofatumumab for Chronic Lymphocytic Leukemia II-34

InNexus's DXL625 Receives Positive Opinion from FDA II-34

Spectrum Pharma Obtains FDA Approval for Zevalin's Expanded

Label in NHL Treatment II-35

Bayer Schering Obtains EU Approval for Zevalin in First-Line

Treatment II-35

7. RECENT INDUSTRY ACTIVITY II-36

Pfizer Discontinues Development of TRU-015; Continues to

Develop SBI-087 II-36

Roche and Biogen Discontinue Ocrelizumab Development in

Rheumatoid Arthritis II-36

Roche and Biogen File Patent Suit Against GSK II-37

Ocrelizumab Meets Primary End-Point In Phase III Trial for RA II-37

Rituxan Plus FC Chemotherapy Shows Improved Survival in

Treatment-Naïve CLL Patients II-37

FDA Declines Early Use of Rituxan in RA II-38

LG Life Sciences Announces New Anti-CD20 Antibody Program II-38

Provenance Acquires Global Rights to New Anti-CD20 Antibody

from Merck II-38

Roche Takes Over Genentech II-39

Pfizer Acquires Wyeth II-39

Spectrum Pharma Acquires Lymphoma Drug Zevalin II-39

Biogen Partners with Genentech and Roche for Development of

GA-101 II-39

Roche, GlycArt and Genentech Team Up for Development of GA-101 II-40

InNexus Biotechnology Discov
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