Blog Archive
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2008
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March
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- Masimo Rainbow SET Pulse CO-Oximetry Effective as ...
- Lilly : US$4.4 Million to the WHO for MDR-TB Progr...
- Nereus Pharmaceuticals : Clinical Trail of NPI-235...
- Masimo : Schiller AG Adopts its Rainbow SET as The...
- Accuray : CyberKnife Radiosurgery Used to Treat Lu...
- Actavis : approval of generic Wellbutrin SR and Zy...
- Merck Statement on the FDA Early Communication of ...
- Kamada : Advancement in its Phase II Trial with Ae...
- EpiCept, Myriad Genetics, Azixa
- Poniard Pharmaceuticals : Additional data presenta...
- AstraZeneca : Phase III Studies Of The Investigati...
- SPO Medical : Shipping PulseOx 6000(TM) and PulseO...
- MicroDose Technologies : Global License to Merck &...
- Mpex Pharmaceuticals : MP-376, Granted U.S. Orphan...
- Arriva Pharmaceuticals : Phase 2b Development of L...
- Cell Therapeutics : European Marketing Authorizati...
- Allegro Diagnostics : to Develop and Commercialize...
- AstraZeneca : Long-Term SYMBICORT® Use In Children...
- Apieron : FDA Clearance of the Insight™ eNO System...
- Genaera : MedImmune Initiation of Phase 2A Trial o...
- MAP Pharmaceuticals : Positive Results From Compar...
- GlobeImmune, Initiation of a Phase 2a Clinical Tri...
- Tongjitang to Enhance Product Portfolio with a Lea...
- AlphaMed Pharmaceuticals has successfully expresse...
- Universal Detection Technology , Anti-Microbial Pr...
- ArQule, Phase 1/2 Clinical Trial Program of ARQ 19...
- Novelos Therapeutics, Pivotal Phase 3 Lung Cancer ...
- Abbott, Genentech, Roche and OSI, Collaboration on...
- Luminex and Abbott, Agreement for Global Distribut...
- Quidel's QuickVue RSV Test : FDA Grants CLIA Waiver
- Altor BioScience , Tissue Factor Antagonists from ...
- Introgen's p53 Immunotherapy INGN 225 in Patients ...
- Inspire, Second Phase 3 Cystic Fibrosis Trial
- Expression Pathology, Research in Identifying Biom...
- Biothera’s Imprime PGG with Avastin Against Cancer
- Response Genetics, ResponseDX Tests to Select Inst...
- Gilead, Aztreonam Lysine 75 mg Powder for Nebulise...
- Alnylam, First Human Proof of Concept for an RNAi ...
- Aerocrine, NIOX MINO: a New Hand-Held Device to Me...
- KaloBios, Phase 1/2 Trial of KB002 Engineered Mono...
- Cerner and UNMHSC, agreement to evaluate dry-powde...
- Talecris Biotherapeutics, 20th Anniversary of Laun...
- Amira Pharmaceuticals and GSK, global agreement fo...
- Asthmatx, Bronchial Thermoplasty in Refractory Ast...
- Orexo, eoxins, new mechanism for asthma and COPD t...
- Boehringer Ingelheim’s BIBW 2992 for the treatment...
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March
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Mar 25, 2008
Cell Therapeutics : European Marketing Authorization Application for XYOTAX
March 4, 2008- Cell Therapeutics, Inc. (CTI) (Nasdaq and MTA: CTIC) announced that it submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (EMEA) for XYOTAX(TM) (paclitaxel poliglumex, CT-2103) for first-line treatment of patients with non-small cell lung cancer (NSCLC) who have ECOG (Eastern Cooperative Oncology Group) performance status 2 (PS2). The application is based on a positive opinion CTI received from the EMEA's Scientific Advice Working Party, which agreed to review the application based on the existing results of the phase III clinical trials of XYOTAX, known as the STELLAR trials... Cell Therapeutics' Press Release -