Research and Markets, the largest resource for market research information in world providing essential market research reports, industry research, industry analysis, forecasts, market studies, company profiles and country reports.
Welcome - Register - Login - Help/FAQ - 0 items View Basket
Worlds Largest Market Research Resource - 1516232 Live Reports
Search Research and Markets
  Search
Enter keywords, a title or
a report id number below.





Advanced   
Register for free email updates of market research
Currency
  Select a currency for use throughout the site



Search Results

Your Search for 'Drug Safety Assessment in Clinical Trials' returned 795 results - Page 1 of 40

  Sort by   
  Sorted by Rank Top-Bottom

Endpoints - Clinical Trials in Dermatology - Inflammatory Lesions Count is the Key Determinant of Success in Acne Vulgaris Clinical Trials  
GBI Research, Jan 2012, Pages: 99
with an emphasis on safety and efficacy details, Phase II and Phase III clinical trial analysis for both completed and ongoing clinical trials, most promising drugs with more emphasis on safety, efficacy


Endpoints - Clinical Trials in Cardiovascular Disorders - Optimal Use of Surrogate Endpoints and Clinical Biomarkers are Key Determinants of Success  
GBI Research, Jan 2012, Pages: 152
of the major marketed cardiovascular drugs, with an emphasis on safety and efficacy details, Phase II and Phase III clinical trial analysis for both completed and ongoing clinical trials, the most promising


Endpoints - Clinical Trials in Autoimmune Disorders - Multiple Primary and Secondary Endpoints are Increasingly Being Applied to Ensure Success  
GBI Research, Feb 2012, Pages: 135
in autoimmune disorders. The report examines different aspects of clinical trial endpoints in autoimmune disorders, such as analysis of major marketed autoimmune drugs with an emphasis on safety and efficacy


Endpoints - Clinical Trials in CNS Disorders - Multiple Endpoints and Ratings Scales are Becoming More Widely Adopted  
GBI Research, Nov 2011, Pages: 216
with an emphasis on safety and efficacy details. Phase II and Phase III clinical trial analysis for both completed and ongoing clinical trials, most promising central nervous system drugs with details on safety


Endpoints-Clinical Trials in Orphan Diseases - Highest Number of Terminated Trials Focused on Mulitiple Myeloma  
GBI Research, Jan 2012, Pages: 118
clinical trials. The report examines different aspects of clinical trial endpoints in orphan diseases, such as analysis of major marketed orphan drugs with an emphasis on safety and efficacy details, Phase


Top R&D Drug Failures - Toxicity and Serious Adverse Events in Late Stage Drug Development are the Major Causes of Drug Failure  
GBI Research, July 2011, Pages: 72
during the course of clinical trials, due to safety and efficacy issues. The decision to discontinue the development of a drug is taken by the health authorities and is based on interim analysis


Post Marketing Clinical Research - REMS, the Latest Reformation due to Post Marketing Surveillance to Enhance Patient Compliance  
GBI Research, Sep 2011, Pages: 82
Post Marketing Clinical Research: Overview 8 3.1 Introduction 8 3.2 Objectives of Post Marketing Clinical Research 9 3.3 Establishing Safety through Clinical Trials 9 3.3.1 Pre-Approval Drug Safety 9 3


Injectable Drug Delivery: Drugs, Devices, Targets, Therapeutics and Forecasts  
Greystone Associates, Jan 2012
Trial Factors Managed Care and Healthcare Economics Injectable Drug Therapeutics – Segment Assessments and Forecasts Anemia Anticoagulants Growth Hormone Deficiency Hepatitis Inflammatory Autoimmune


The Impact of Cardiac Safety on the Regulatory Landscape: Recent Case Studies  
Decision Resources, Inc., Nov 2011
to limit cardiovascular risk? Scope: - Regulatory environment: The FDA and the International Conference on Harmonisation guidelines, preclinical and clinical cardiac safety assessments. - Postmarketing


Advances in the Design and Regulation of Adaptive Clinical Trials  
Business Insights, Nov 2010, Pages: 129
of compounds. - Assess how the FDA’s draft guidelines on adaptive trials are influencing companies to use adaptive trials in their drug development programs. - Evaluate the providers of key skills


Can Denosumab Achieve Superiority For The Prevention Of SREs In Cancer?  
FirstLine Consulting Group, Feb 2009, Pages: 47
Can Denosumab Achieve Superiority For The Prevention Of SREs In Cancer? There are many large clinical trials currently being conducted with denosumab. It is being tested in osteoporosis, treatment


Prospects for the Phase III Bapineuzumab Trial  
FirstLine Consulting Group, Sep 2009, Pages: 37
of the trial. In our analysis, we have: - Researched bapineuzumab phase I and phase II results in depth, and collected vast amounts of information that have helped us assess the true risk to safety


Pharmaceutical Partnership Deal Terminations  
GBI Research, Sep 2011, Pages: 119
or acquisition activities, or due to a revision of its existing product pipeline. Other causes for the termination of deals included negative results in clinical trials designed to evaluate the safety and efficacy


Will Anyone Crack the Obesity Drug Market?  
Espicom Business Intelligence Ltd, Feb 2011, Pages: 102
combination, Contrave. The market was then surprised when the FDA did not approve the drug, asking instead for further clinical trials. If Contrave had been approved, it would have been the first new


Innovations and Trends in Clinical Trials - Microdosing (Phase 0 Trials), Adaptive Trials, Phase IV Trials and the Role of Information Technology  
Arrowhead Publishers, March 2007, Pages: 149
discovery process by identifying failures at an earlier stage. This report provides detailed information regarding new developments in the field of clinical trials as well as an assessment of the impact


Enabling Innovation: Drug Development Through Biomarker Validation and Qualification  
Decision Resources, Inc., March 2011, Pages: 22
biomarker programs alongside drug discovery and development because biomarkers can aid in discovery of drug targets, assess drug safety and efficacy, stratify patients in clinical trials, and facilitate go


Biomarkers in Late Stage Clinical Trials: Applications, Opportunities and Activities of Leading Players  
Business Insights, April 2010, Pages: 178
reduce the attrition rate of late stage clinical trials by assessing drug potential in terms of efficacy and toxicity at the early stages of the clinical development. Thus, biomarkers significantly


Will Next Generation Oral Anticoagulants Replace Warfarin as Mainstay Therapy?  
MP Advisors, Aug 2011
comparison major anticoagulants in DVT treatment - Clinical Data comparison major anticoagulants in ACS Liver Toxicity Long term safety concern: Liver Toxicity Assessment of Bleeding Risk - Clinical Data


R&D Trends: Obesity - 2006-2011: Obesity's Lean Years  
Datamonitor, May 2011, Pages: 40
and target product profiles necessary for success in the obesity market - Assess the challenges faced in treating obesity and the future direction for obesity therapy - Provide insight into clinical trial


Early Stage Drug Safety Strategies and Risk Management: Maximizing Opportunities Towards Achieving Clinical Success  
Business Insights, April 2009, Pages: 159
rare events that are unlikely to be identified in clinical trials. Major pharma companies have subsequently begun to implement an array of new technologies for drug safety prediction into the discovery


Results:  First -   Prev -   1 -   2 -   3 -   4 -   5 -   6 -   Next -   Last


For enquiries please call us on:
  +353-1-415-1241 (GMT Office Hours)
  1-800-526-8630 (US/Canada Toll Free)
  1-917-300-0470 (EST Office Hours)

   All rights reserved. © Copyright 2012 Research and Markets
   Terms and conditions Privacy Policy Publishers Employment Opportunities Site Map Link to us Webmaster Affiliate Network


Research and Markets RSS Feeds