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Cell Therapeutics, Inc. (CTI) Plans to Submit Supplemental Biologics License Application (sBLA) for ZEVALIN(R) Consolidation of First Remission in Advanced Stage Follicular Lymphoma in 2008
Date:11/27/2007

e a presentation by CTI on pixantrone and 29 presentations by Biogen Idec and Bayer-Schering on ZEVALIN(R). Selected ZEVALIN presentations are included below.

Date Time Poster # Title

(Abstract#)

Saturday,

December 8, 5:30 #236-I The Impact of Incorporating Targeted

2007 PM (1082) Radioimmunotherapy (RIT) into

Transplant Preparative Regimens on

the Incidence of Therapy Related

Myelodysplasia (t-MDS) or AML (t-AML)

Following Autologous Stem Cell

Transplant (ASCT) for Lymphoma.

Sunday, 5:15 Oral Session 90Yttrium Ibritumomab Tiuxetan

Dec. 9, PM (22) (Zevalin) Combined with BEAM (Z -

2007 BEAM) Conditioning Regimen Plus

Autologous Stem Cell Transplantation

in Relapsed or Refractory Follicular

Lymphoma. GELA Phase II Study.

Monday, 12:00 Oral Session Phase II Study of R-CHOP Followed by

December 10, PM (389) 90Y-Ibritumomab Tiuxetan in Untreated

2007 Mantle Cell Lymphoma: Eastern

Cooperative Oncology Group Study

E1499.

Monday, 3:30 Oral Session 90Y-Ibritumomab Tiuxetan (ZEVALIN)

Dec. 10, PM (643) Consolidation of First Remission

2007 in Advanced Stage Follicular

Non-Hodgkins Lymphoma: First Results

of the Internat
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SOURCE Cell Therapeutics, Inc.
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