xenoport inc (XNPT:NASDAQ GS)
xenoport inc (XNPT) Snapshot
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Open
$5.41
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Previous Close
$5.43
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Day High
$5.43
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Day Low
$5.22
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52 Week High
10/5/12 - $12.98
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52 Week Low
06/7/13 - $4.93
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Market Cap
250.8M
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Average Volume 10 Days
538.7K
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EPS TTM
$-1.50
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Shares Outstanding
47.4M
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EX-Date
--
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P/E TM
--
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Dividend
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Dividend Yield
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Related News
xenoport inc (XNPT) Related Businessweek News
No Related Businessweek News Foundxenoport inc (XNPT) Details
XenoPort, Inc., a biopharmaceutical company, focuses on developing and commercializing a portfolio of internally discovered product candidates for the treatment of neurological disorders. The company markets Gabapentin Enacarbil extended-release tablets for the treatment of moderate-to-severe primary restless legs syndrome and for the management of postherpetic neuralgia in adults under the Regnite name in Japan and five other Asian countries. The company’s lead product candidate is Arbaclofen Placarbil, a transported prodrug of R-baclofen that is in Phase III clinical trial for the potential treatment of spasticity in patients with multiple sclerosis (MS), stroke and cerebral palsy, and spinal cord injury. Its product candidates in clinical development also include XP21279, a transported prodrug of Levodopa, which has completed Phase II clinical trial for the treatment of Parkinson’s disease; and XP23829, a prodrug of monomethyl fumarate that is in Phase I clinical trial for the potential treatment of relapsing-remitting MS, psoriasis, and/or other disorders. The company has strategic alliance with Astellas Pharma Inc. to develop and commercialize Gabapentin Enacarbil under the Regnite name in Japan, Korea, the Philippines, Indonesia, Thailand, and Taiwan. XenoPort, Inc. was founded in 1999 and is based in Santa Clara, California.
xenoport inc (XNPT) Top Compensated Officers
xenoport inc (XNPT) Key Developments
Xenoport, Inc. reported top-line results from its pivotal Phase 3 clinical trial of Arbaclofen Placarbil for the treatment of patients with spasticity due to multiple sclerosis. The trial was unsuccessful in demonstrating that AP provided statistically significant improvement relative to placebo in the co-primary endpoints of the study. The company also announced that as a result of the study, it has decided to terminate further investment in the AP program. The company will be working diligently to shut down all activities related to AP development, and the company plans to provide an update in the future on the impact of these expected savings on its cash burn guidance. The trial was a 13-week, multicenter, randomized, double-blind, placebo-controlled study that enrolled 228 subjects in 30 sites in the United States. Eligible subjects were randomized to one of four arms: 15 mg, 30 mg or 45 mg of AP or placebo dosed twice a day with food.
To discuss its AP Phase 3 clinical trial results and business updates
Xenoport, Inc. announced that shipments of Horizant(R) (gabapentin enacarbil) Extended-Release Tablets to its distributor in the United States have commenced. Depending on individual pharmacy ordering patterns, the product is anticipated to be generally available to patients in the first week of June.

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Industry Analysis
XNPT
Industry Average
| Valuation | XNPT | Industry Range |
| Price/Earnings | NM | Not Meaningful |
| Price/Sales | 21.9x |
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| Price/Book | 2.4x |
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| Price/Cash Flow | NM | Not Meaningful |
| TEV/Sales | 12.2x |
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Post a JobJobs
- Santa Clara, CA | XenoportPosted: Apr 03
- Santa Clara, CA | XenoportPosted: May 19
- Santa Clara, CA | XenoportPosted: Mar 26
- Santa Clara, CA | XenoportPosted: May 13
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