Last $2.30 USD
Change Today +0.005 / 0.22%
Volume 112.4K
OGXI On Other Exchanges
Symbol
Exchange
Munich
NASDAQ CM
As of 8:10 PM 02/27/15 All times are local (Market data is delayed by at least 15 minutes).

oncogenex pharmaceutical inc (OGXI) Snapshot

Open
$2.30
Previous Close
$2.29
Day High
$2.36
Day Low
$2.25
52 Week High
03/11/14 - $14.25
52 Week Low
02/4/15 - $1.92
Market Cap
48.8M
Average Volume 10 Days
147.1K
EPS TTM
$-1.74
Shares Outstanding
21.3M
EX-Date
--
P/E TM
--
Dividend
--
Dividend Yield
--
Current Stock Chart for ONCOGENEX PHARMACEUTICAL INC (OGXI)

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oncogenex pharmaceutical inc (OGXI) Details

OncoGenex Pharmaceuticals, Inc., a biopharmaceutical company, develops and commercializes therapies that address treatment resistance in cancer patients. Its lead drug candidate, Custirsen is in Phase III clinical development for the treatment in men with metastatic castrate-resistant prostate cancer, and in patients with advanced, unresectable non-small cell lung cancer. Custirsen is an experimental drug designed to block the production of the protein clusterin, which may play a fundamental role in cancer cell survival and treatment resistance. The company also develops Apatorsen, which is in seven randomized Phase II trials for the treatment of bladder, lung, pancreatic, and prostate cancers. Apatorsen is an investigational drug designed to inhibit the production of heat shock protein (Hsp27), a protein that is elevated in various cancers and that has been shown to promote cancer cell growth and tumor metastasis. In addition, it develops OGX-225 that is in pre-clinical development for the treatment of solid tumors. The company has a collaboration and license agreement with Teva Pharmaceutical Industries Ltd. to develop and commercialize Custirsen. The company is headquartered in Bothell, Washington.

37 Employees
Last Reported Date: 03/11/14

oncogenex pharmaceutical inc (OGXI) Top Compensated Officers

Founder, Chief Executive Officer, President, ...
Total Annual Compensation: $503.7K
Chief Medical Officer and Executive Vice Pres...
Total Annual Compensation: $403.1K
Compensation as of Fiscal Year 2013.

oncogenex pharmaceutical inc (OGXI) Key Developments

OncoGenex Pharmaceuticals, Inc. and Sarah Cannon Announce Completion of Patient Enrollment in the Spruce(TM) Clinical Trial Evaluating Apatorsen

OncoGenex Pharmaceuticals, Inc. and Sarah Cannon announced that patient enrollment has been completed in the Spruce(TM) clinical trial, an investigator-sponsored, randomized, placebo-controlled Phase 2 trial evaluating apatorsen in combination with carboplatin and pemetrexed in patients with previously untreated, advanced, non-squamous, non-small cell lung cancer (NSCLC). In the Spruce trial, approximately 155 patients were randomized to receive either apatorsen or placebo in combination with carboplatin and pemetrexed therapy. The primary objective of the trial is progression-free survival (PFS), with additional analyses to evaluate overall survival, tumor response rates, safety, tolerability and the effect of therapy on heat shock protein 27 (Hsp27) levels.

OncoGenex Pharmaceuticals Executes New Lease Agreements Enabling Relocation of its Bothell, Washington Headquarters

OncoGenex Pharmaceuticals, Inc. announced that it has executed new lease agreements enabling the relocation of its Bothell, Washington headquarters. Effective March 1, 2015, OncoGenex' new corporate headquarters will be located at 19820 North Creek Parkway, approximately three miles from the company's current location. The final lease agreements were executed on Feb. 11, 2015, and are subject to certain closing conditions.

OncoGenex Pharmaceuticals, Inc. Announces Results from Phase 2 Borealis-1 Trial

On December 19, 2014, OncoGenex Pharmaceuticals, Inc. announced results from the randomized, controlled Phase 2 Borealis-1 trial evaluating low and high dose (600mg and 1,000mg) apatorsen in combination with gemcitabine/cisplatin chemotherapy compared to chemotherapy alone in the treatment of metastatic bladder cancer. Overall trial results indicated that the addition of 600mg apatorsen to standard of care chemotherapy showed a 14% reduction in risk of death (overall survival hazard ratio (HR) = 0.86) and a 17% reduction in progressive disease and death (progression-free survival HR = 0.83) when compared to chemotherapy alone. Over one-third of the patients in the trial had lower performance status, as defined by a Karnofsky score of 80% or less. These patients derived the benefit from 600mg apatorsen in combination with chemotherapy, resulting in a 50% reduction in risk of death (overall survival HR = 0.50) compared to chemotherapy alone. Less benefit was observed in the 1,000mg apatorsen arm due to increased adverse events to a higher rate of discontinuation of both apatorsen and chemotherapy. Apatorsen 600mg was well tolerated in combination with chemotherapy. OncoGenex will be working closely with investigators and regulatory agencies to determine next steps.

 

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