Aeterna Zentaris Stock Chart Analysis Video(0) Three straight days of closing ahead has the AEterna Zentaris chart on watch for continued upward pressure. Shares rose 8.5 percent on Tuesday to close near the high of the day on increased volume, which is a bullish sign as the stock nears resistance. Shares traded as low as $1.75 last week, but have recovered to close on Tuesday at $2.16 on Read More |
Aeterna Zentaris Continues Pursuing Drug Development for Multiple Myeloma(0) The path to bring a new cancer drug to market can certainly be a long and bumpy road full of twists and turns. It was about one month ago that the news hit of Aeterna Zentaris (TSX: AEZ)(NASDAQ: AEZS) and Keryx Biopharmaceuticals (NASDAQ: KERX) terminating their license agreement with respect to perifosine, an Akt inhibiting oral anticancer compound; giving back full North American rights to Aeterna. Read More |
Keryx Phase II Colorectal Cancer Results in Journal of Clinical Oncology(0) Keryx Biopharmaceuticals, Inc. (NASDAQ:KERX) reported recently that a manuscript entitled “Randomized Placebo-Controlled Phase II Trial of Perifosine Plus Capecitabine as Second- or Third-Line Therapy in Patients with Metastatic Colorectal Cancer” reporting Phase 2 activity of KRX-0401 (perifosine) in the treatment of patients with refractory, advanced colorectal cancer (mCRC), was selected for publication in the October 3, 2011 online edition of the Journal of Clinical Oncology. Efficacy data from this study was presented in June 2010 at the 46th Annual Meeting of the American Society of Clinical Oncology. According to the press release on Keryx’s website, “Based on the data, in which the combination of P-CAP demonstrated statistical significance with respect to median overall survival and median time to tumor progression, the investigators concluded that the P-CAP combination showed promising clinical activity compared to single-agent capecitabine, and that the difference in clinical outcome seen with the addition of perifosine was impressive.” Keryx is currently investigating perifosine as a novel, potentially first-in-class, oral anti-cancer drug candidate that inhibits Akt activation in the phosphoinositide 3-kinase (PI3K) pathway under a Special Protocol Assessment and with Fast Track designation from the Food and Drug Administration in a Phase 3 trial. Enrollment was completed in July of 2011 for the trial entitled “X-PECT” (Xeloda® + Perifosine Evaluation in Colorectal cancer Treatment) with completion expected in the first quarter of 2012. KRX-0401 (perifosine) is in-licensed by Keryx from Aeterna Zentaris Inc. (NASDAQ:AEZS) in the United States, Canada and Mexico. Keryx Biopharmaceuticals (KERX) Stock Quote and News:
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Zack’s Notes Keryx (KERX) Uptrend and 67% Change in 52 Week(0)
Zacks.com, a leader in investment research, has aptly noted the recent uptrend in the share price of Keryx Biopharmaceuticals over the last several weeks. Zack’s “SmarTrend” analyzes over 5,000 securities simultaneously throughout the trading day and provides its subscribers with trend change alerts in real time. According to Zack’s commentary on April 5, 2011,
Keryx Biopharmaceuticals is focused on the acquisition, development and commercialization of medically important pharmaceutical products for the treatment of cancer and renal disease. Keryx is developing KRX-0401 (perifosine), a novel, potentially first-in-class, oral anti-cancer agent that inhibits Akt activation in the phosphoinositide 3-kinase (PI3K) pathway, and also affects a number of other key signal transduction pathways, including the JNK pathway, all of which are pathways associated with programmed cell death, cell growth, cell differentiation and cell survival. KRX-0401 has demonstrated both safety and clinical efficacy in several tumor types, both as a single agent and in combination with novel therapies. KRX-0401 is currently in Phase 3 clinical development for both refractory advanced colorectal cancer and multiple myeloma, and in Phase 1 and 2 clinical development for several other tumor types. Each of the KRX-0401 Phase 3 studies is being conducted under a Special Protocol Assessment (SPA) agreement with the FDA. Keryx is also developing Zerenex (ferric citrate), an oral, ferric iron-based compound that has the capacity to bind to phosphate and form non-absorbable complexes. The Phase 3 clinical program of Zerenex in the treatment for hyperphosphatemia (elevated phosphate levels) in patients with end-stage renal disease is being conducted pursuant to an SPA agreement with the FDA. Keryx is headquartered in New York City. Keryx Biopharmaceuticals (KERX) Stock Quote and News:
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