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Anesiva 
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A small selected sample of reports and related news headlines for Anesiva are available below. Free sample reports are also available for other Companies.

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PIPELINE ANALYSIS - Sales Forecasts available to EvaluatePharma Subscribers

 
  Rank Product Therapeutic Category Therapeutic Subcategory Pharmacological Class Phase (Current)
Anesiva 1 Adlea Central Nervous System Non-narcotic analgesics Non-narcotic analgesic Phase III
  - LT-1951 Cardiovascular Other cardiovasculars Arginine supplement Phase I

FINANCIAL DATA ($US mln) - Forecasts available to EvaluatePharma Subscribers

Anesiva
  2005 2006
 Valuation Measures
  Based on Latest Share Prices
     Valuing the Equity
       Market Capitalisation 144 144
       PE Ratio (diluted) - Normalised (x) (0.2) (1.3)
 
     Valuing the Enterprise
       Enterprise Value 64 64
       Free Cash Flow (Pre-Dividends) (26) (53)
       FCF Yield (%) (39.7%) (82.0%)
 
 Forecast Financials
  Income Statement
     Total Revenues 0 0
     S,G & A (17) (24)
     R&D (19) (35)
     Other Income/ Expense - Net 0 0
     EBIT - Normalised (37) (59)
     Net Interest & Financial Items 1 3
     Pre-tax Profits - Normalised (35) (56)
     Income Before Taxes (35) (56)
     Tax 0 0
     Tax Rate (%) 0.0% 0.0%
     Extraordinary 2 -
     Net Income - Reported (34) (56)
     Net Income - Normalised (35) (56)
 
  Per Share Data
     EPS - Diluted (16.89) (2.69)
     EPS - Basic (16.89) (2.69)
     EPS - Normalised (diluted) (17.76) (2.69)
     EPS - Normalised (basic) (17.76) (2.69)
     Avg. Shares Outstanding - Diluted 2.0 20.6
     Avg. Shares Outstanding - Basic 2.0 20.6
     DPS 0.00 0.00

NEWS - Selected Product News Headlines (as of 11 June 2008)

Anesiva Announces South Korea FDA Approval of Adlea(TM) Investigational New Drug Application   (Anesiva)   03-Jun-2008
FDA Accepts Zingo(TM) Supplemental New Drug Application to Reduce Pain Associated With Peripheral Needle Insertion Procedures in Adults   (Anesiva)   21-May-2008
Anesiva Announces Publication of Phase 3 Zingo(TM) Data in the Journal Pediatrics   (Anesiva)   05-May-2008
Anesiva Announces Pivotal Phase 3 Clinical Trial of Adlea(TM) for Reducing Post-Surgical Pain Following Total Knee Replacement   (Anesiva)   08-Apr-2008
Anesiva Commences Phase 3 Clinical Trial of Adlea(TM) for Reducing Post-Surgical Pain Following Bunionectomy   (Anesiva)   25-Mar-2008
Anesiva Announces Submission of Supplemental New Drug Application for Zingo(TM) to Reduce Pain Associated With Needle Insertion Procedures in Adults   (Anesiva)   10-Mar-2008
Anesiva Announces Pivotal Phase 3 Trial of Zingo(TM) Meets Primary Endpoint and Significantly Reduces Venous Access Pain in Adults   (Anesiva)   16-Oct-2007
Anesiva Outlines Comprehensive Commercialization Plan for FDA Approved Product Zingo(TM)   (Anesiva)   12-Oct-2007
Anesiva Defines Regulatory Pathway for Adlea with FDA   (Anesiva)   10-Oct-2007
Anesiva Initiates Phase 2 Trial with Adlea(TM) for Pain Relief Following Total Hip Replacement Surgery   (Anesiva)   04-Oct-2007
Anesiva Initiates New Phase 2 Trial of Adlea(TM) for Pain Relief Following Knee Replacement Surgery   (Anesiva)   13-Sep-2007
Anesiva Completes Enrollment in Phase 3 Clinical Trial of Zingo(TM) to Treat Pain Associated With Venous Access Procedures in Adults   (Anesiva)   28-Aug-2007
Anesiva Receives FDA Approval for Zingo(TM), a New, Innovative Product to Reduce Pain Associated with Needle Insertion Procedures in Children   (Anesiva)   17-Aug-2007
Anesiva Announces Phase 2 Data Showing Substantial, Long-Term Pain Reductions with Adlea(TM) (formerly 4975) in Osteoarthritis of the Knee   (Anesiva)   02-Jul-2007

IN-DEPTH COMPETITIVE INTELLIGENCE AVAILABLE ON

 
  Product Generic Name
Anesiva 1207 (ALGRX 1207) -
  Adlea -
  ALGRX 2872 -
  Antibiotic Aptamer -
  Avrina -
  HIF Decoy -
  LT-1951 L-arginine
  Zingo lidocaine
 
EvaluatePharma® provides historic and forecast sales from 1986 to 2012 for worldwide and US Rx (prescription drugs) and OTC drugs. EvaluatePharma® analysts continuously update company models from SEC filings, annual reports, investor/analyst presentations, company press releases, FDA and USPTO. Consensus forecasts for marketed and emerging products are built-up using recent research reports from top equity analysts.

Analyse pharma and biotech products by market status or development phase (e.g., preclinical, phase I, phase II, phase III, filed, approved, withdrawn, disposed etc), therapeutic category, product sourcing strategy, patent expiry and patent life remaining, originator, technology, indication, pharmacological class, deal dates, deal types and partners, launch dates, FDA approval data and new molecular entity (NME) age - plus many more data items and analytics unique to EvaluatePharma®.

Aggregations of these measures at a high-level means that companies may be ranked against each other on items such as: market capitalization, patent risk, R&D spend, freshness index, sales strategy (inlicensed vs organic sales), sales by therapy area or technology and various other concentration measures. These aggregations make EvaluatePharma® ideal for competitive benchmarking, ranking and Peer Group analysis.

Note: When a merger or acquisition is agreed, a virtual merged Company will be added to the list of available Company reports. Any information presented for a virtual merged company is for illustrative purposes, only.

Source: EvaluatePharma ® Generated at 13:54:40 (GMT) on 11-Jun-2008 © 2008 EvaluatePharma Ltd