Cytori Therapeutics, Inc. develops cellular therapeutics for specific diseases and medical conditions.
CYTX primarily provides Cytori Cell Therapy, which is in Phase III pivotal clinical trial for the treatment of impaired hand function in scleroderma.
CYTX offers Celution System devices, proprietary enzymes, and sterile consumable sets that are used at the point-of-therapeutic application or at an off-site processing center; and StemSource cell and tissue banking systems, as well as surgical accessories and instruments.
CYTX also provides ATI-0918, a liposomal encapsulation of doxorubicin for use in treating breast cancer, ovarian cancer, multiple myeloma, and Kaposi's sarcoma; and ATI-1123, a liposomal formulation of docetaxel for the treatment of non-small cell lung cancer, breast cancer, squamous cell carcinoma of the head and neck cancer, gastric adenocarcinoma, and hormone refractory prostate cancer.
The company was founded in 1996 and is headquartered in San Diego, California.
August 7, 2014
Cytori (CYTX) has a credibility issue
August 7, 2014
RegMed – The profit takers are out
August 7, 2014
Higher open expected, RegMed, a few hullabaloos this week
August 6, 2014
RegMed notches up another victory
August 6, 2014
RegMed - Cytori (CYTX) is the talk of the airwaves
August 5, 2014
CYTORI (CYTX) puts ATHENA and ATHENA II TRIALS on CLINICAL HOLD followed by a -22.38% share price drop
August 5, 2014
Lower open expected; could Cytori's (CYTX) clinical HOLD penalize the sector?
August 5, 2014
RegMed - somedays it's just dumb luck
August 5, 2014
RegMed battling to stay positive
August 5, 2014
Lower open expected; RegMed barely bounces
35 companies, 1 interpreter!
Insight, foresight and recommendation
Cytori (CYTX) – Started the year seeking "strategic alternatives" with a share priced at $0.29, seeing a couple of highs of $0.47 with a 2/1 value of $0.40 which has been dropping and currently (2/16) at $0.32. A sory of missed oppurtunity thrown at the feet of its CEO ... incremental development news are minimal ... it's all about whether the FDA requests ... MORE data and trial.
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