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Cell Therapeutics Inc. (CTIC)
Oncology Corporate Profile

  • Products & Overview
  • Recent News

HQ Location

501 Elliott Avenue West, Suite 400
Seattle, WA 98119

Company Description

CTI's goal is to build a leading biopharmaceutical company with a diversified portfolio of proprietary oncology drugs. CTI focuses on the research, development, acquisition and in-licensing activities to identify and develop new, less toxic and more effective ways to treat cancer.

Website: http://www.cticseattle.com

Commercial Products

This company does not have any commercial products

Pipeline Products

  • Brand
  • Generic
  • Investigational
Brand / Product Class Area of Study Phase Partnership
pixantrone / BBR 2778anthracycline2nd line diffuse large B-cell Non-Hodgkin's Lymphoma (NHL)III
Opaxio™ / paclitaxel poliglumex / CT-2103microtubule inhibitorNon Small Cell Lung Cancer (NSCLC)III
Opaxio™ / paclitaxel poliglumex / CT-2103microtubule inhibitorOvarian cancerIII
brostallicinDNA minor groove binding agent (synthetic)Soft tissue sarcomaII
Opaxio™ / paclitaxel poliglumex / CT-2103microtubule inhibitorEsophageal cancerII
CT-3610dinuclear-platinum complexVarious cancer typesPreclinical
UnnamedHIF-1 inhibitorVarious cancer typesResearch

View additional information on product candidates here »


Recent News Headlines

[Business Wire] - CHICAGO----Zacks.com Analyst Blog features: Deutsche Bank AG , Credit Suisse Group , JPMorgan Chase & Co. , Citigroup Inc. and Cell Therapeutics .

[Zacks] - Cell Therapeutics Inc. receives validation from the European Medicines Agency for the expanded Pediatric Investigation Plan filed for its lead candidate pixantrone.

[GlobeNewswire] - DALLAS -- MicroStockProfit.com announces an investment report featuring Cell Therapeutics Inc. . The report includes financial, comparative and investment analyses, and industry information you need to know to make an educated investment decision.

[PR Newswire] - Cell Therapeutics, Inc. announced today that it has received notice that the European Medicines Agency has validated the expanded Pediatric Investigation Plan that CTI filed in July for pixantrone for the treatment of relapsed or refractory, aggressive non-Hodgkin's lymphoma .  Following the validation, the EMEA Pediatric Committee will review and comment or approve the content of pediatric plan.  Once the PIP is approved, CTI will submit the Marketing Authorization Application for pixantrone in the E.U. later this year.  The pediatric program will study pixantrone in pediatric patients aged 6 months to 18 years with the goal of determining the comparative safety and effectiveness of pixantrone compared to doxorubicin in pediatric lymphoid cancers.

[Zacks] - Cell Therapeutics' second quarter 2010 net loss increased to $53.6 million from a loss of $27.4 million in the corresponding period in 2009.

[PR Newswire] - Cell Therapeutics, Inc. today reported recent accomplishments and financial results for the second quarter ended June 30, 2010.

[PR Newswire] - Cell Therapeutics, Inc. today announced it has filed for a Special Protocol Assessment with the U.S. Food and Drug Administration for the design of its new phase III trial of pixantrone for patients with relapsed or refractory aggressive B-Cell non-Hodgkin's lymphoma .

[PR Newswire] - On Thursday, August 5, 2010, at 8:30 a.m. Eastern/2:30 p.m. Central European/5:30 a.m. Pacific, members of Cell Therapeutics, Inc.'s management team will host a conference call to discuss the Company's second quarter 2010 accomplishments and financial results.

Cell Therapeutics, Inc. today announced the successful closing of its previously announced sale of $4.06 million of securities to an accredited investor in a private offering pursuant to Section 4 of the Securities Act of 1933, as amended.  The sold securities consist of 4,060 shares of Series 6 preferred stock, no par value per share, together with warrants to purchase an aggregate of 5.8 million shares of common stock.  Prior to the closing date, the investor elected to convert all of its shares of Series 6 preferred stock and to receive the 11.6 million shares of the Company's common stock issuable upon such conversion at the closing. Â