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Lynn49 
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Joined: 11 April 2007
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 Topic: New Online Registry for People with Lupus
Posted: 02 November 2010 at 2:32am |
People with lupus nationwide can now sign up to be notified of local clinical studies enrolling volunteers through the Lupus Foundation of America's (LFA) Center for Clinical Trials Education (CCTE). The LFA's Lupus Research Registry, through the CCTE, uses information provided by the registrants to help connect them to local clinical studies. The Lupus Research Registry is part of the LFA's ongoing efforts to advance the medicine and science of lupus and further the discovery of safe, effective, and more tolerable treatments for lupus.
The LFA is committed to bringing down barriers that have impeded progress in lupus research. In recent years, the number of clinical trials for potential new lupus treatments has risen, increasing the demand for volunteers. The Lupus Research Registry provides a valuable tool for people with lupus to learn about opportunities to participate in a clinical study. The Registry also helps clinical investigators connect with potential participants for various types of studies, such as the genetic origins of lupus and new procedures used to monitor the disease and response to treatment.
"We continue to receive more requests from clinical investigators for people with lupus to serve as study volunteers and we know that it is only through increased participation that we will continue to move toward having a full arsenal of treatments needed for a disease as diverse and complex as lupus," said Sandra C. Raymond, President and CEO of the Lupus Foundation of America. "The LFA's Lupus Research Registry will make the link between the trials and potential participants stronger; ensuring the community is informed and engaged in the quest for new treatments, and ultimately a cure."
The LFA first launched the CCTE in 2008 and with the addition of the Lupus Research Registry it is now positioned to meet a growing need for clinical research participation. This is a result of greater interest from the pharmaceutical and biotechnology industry in developing new therapies for lupus. Individuals interested in joining the LFA's Lupus Research Registry can do so by completing a simple online form here.
Source:
Lupus Foundation of America http://www.medicalnewstoday.com/articles/206006.php
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Believe those who are seeking the truth. Doubt those who find it.
Andre Gide
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Lynn49
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Posted: 21 January 2011 at 5:47pm |
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bump
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Believe those who are seeking the truth. Doubt those who find it.
Andre Gide
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ronbn56
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Posted: 27 January 2011 at 11:48am |
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66
Edited by ronbn56 - 09 March 2011 at 8:15pm
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LEGAL PRESCRIBED DRUGS USED AS THE DOCTOR ORDERED IS THE 4TH LEADING CAUSE OF DEATH IN THE USA.
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Lynn49
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Joined: 11 April 2007
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Posts: 6032
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Posted: 27 January 2011 at 11:51am |
People with lupus nationwide can now sign up to be notified of local clinical studies enrolling volunteers through the Lupus Foundation of America's (LFA) Center for Clinical Trials Education (CCTE). The LFA's Lupus Research Registry, through the CCTE, uses information provided by the registrants to help connect them to local clinical studies. The Lupus Research Registry is part of the LFA's ongoing efforts to advance the medicine and science of lupus and further the discovery of safe, effective, and more tolerable treatments for lupus.
The LFA is committed to bringing down barriers that have impeded progress in lupus research. In recent years, the number of clinical trials for potential new lupus treatments has risen, increasing the demand for volunteers. The Lupus Research Registry provides a valuable tool for people with lupus to learn about opportunities to participate in a clinical study. The Registry also helps clinical investigators connect with potential participants for various types of studies, such as the genetic origins of lupus and new procedures used to monitor the disease and response to treatment.
"We continue to receive more requests from clinical investigators for people with lupus to serve as study volunteers and we know that it is only through increased participation that we will continue to move toward having a full arsenal of treatments needed for a disease as diverse and complex as lupus," said Sandra C. Raymond, President and CEO of the Lupus Foundation of America. "The LFA's Lupus Research Registry will make the link between the trials and potential participants stronger; ensuring the community is informed and engaged in the quest for new treatments, and ultimately a cure."
The LFA first launched the CCTE in 2008 and with the addition of the Lupus Research Registry it is now positioned to meet a growing need for clinical research participation. This is a result of greater interest from the pharmaceutical and biotechnology industry in developing new therapies for lupus. Individuals interested in joining the LFA's Lupus Research Registry can do so by completing a simple online form here.
Source:
Lupus Foundation of America http://www.medicalnewstoday.com/articles/206006.php
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Believe those who are seeking the truth. Doubt those who find it.
Andre Gide
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clarky14
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Joined: 21 February 2007
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Posts: 204
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Posted: 02 May 2011 at 1:34pm |
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People with lupus nationwide can now sign up to be notified of local clinical studies enrolling volunteers through the Lupus Foundation of America's (LFA) Center for Clinical Trials Education (CCTE). The LFA's Lupus Research Registry, through the CCTE, uses information provided by the registrants to help connect them to local clinical studies. The Lupus Research Registry is part of the LFA's ongoing efforts to advance the medicine and science of lupus and further the discovery of safe, effective, and more tolerable treatments for lupus.
The LFA is committed to bringing down barriers that have impeded progress in lupus research. In recent years, the number of clinical trials for potential new lupus treatments has risen, increasing the demand for volunteers. The Lupus Research Registry provides a valuable tool for people with lupus to learn about opportunities to participate in a clinical study. The Registry also helps clinical investigators connect with potential participants for various types of studies, such as the genetic origins of lupus and new procedures used to monitor the disease and response to treatment.
"We continue to receive more requests from clinical investigators for people with lupus to serve as study volunteers and we know that it is only through increased participation that we will continue to move toward having a full arsenal of treatments needed for a disease as diverse and complex as lupus," said Sandra C. Raymond, President and CEO of the Lupus Foundation of America. "The LFA's Lupus Research Registry will make the link between the trials and potential participants stronger; ensuring the community is informed and engaged in the quest for new treatments, and ultimately a cure."
The LFA first launched the CCTE in 2008 and with the addition of the Lupus Research Registry it is now positioned to meet a growing need for clinical research participation. This is a result of greater interest from the pharmaceutical and biotechnology industry in developing new therapies for lupus. Individuals interested in joining the LFA's Lupus Research Registry can do so by completing a simple online form here.
Source:
Lupus Foundation of America
http://www.medicalnewstoday.com/articles/206006.php
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Lynn49
Senior Member
Joined: 11 April 2007
Online Status: Offline
Posts: 6032
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Quote Reply
Posted: 02 May 2011 at 1:50pm |
People with lupus nationwide can now sign up to be notified of local clinical studies enrolling volunteers through the Lupus Foundation of America's (LFA) Center for Clinical Trials Education (CCTE). The LFA's Lupus Research Registry, through the CCTE, uses information provided by the registrants to help connect them to local clinical studies. The Lupus Research Registry is part of the LFA's ongoing efforts to advance the medicine and science of lupus and further the discovery of safe, effective, and more tolerable treatments for lupus.
The LFA is committed to bringing down barriers that have impeded progress in lupus research. In recent years, the number of clinical trials for potential new lupus treatments has risen, increasing the demand for volunteers. The Lupus Research Registry provides a valuable tool for people with lupus to learn about opportunities to participate in a clinical study. The Registry also helps clinical investigators connect with potential participants for various types of studies, such as the genetic origins of lupus and new procedures used to monitor the disease and response to treatment.
"We continue to receive more requests from clinical investigators for people with lupus to serve as study volunteers and we know that it is only through increased participation that we will continue to move toward having a full arsenal of treatments needed for a disease as diverse and complex as lupus," said Sandra C. Raymond, President and CEO of the Lupus Foundation of America. "The LFA's Lupus Research Registry will make the link between the trials and potential participants stronger; ensuring the community is informed and engaged in the quest for new treatments, and ultimately a cure."
The LFA first launched the CCTE in 2008 and with the addition of the Lupus Research Registry it is now positioned to meet a growing need for clinical research participation. This is a result of greater interest from the pharmaceutical and biotechnology industry in developing new therapies for lupus. Individuals interested in joining the LFA's Lupus Research Registry can do so by completing a simple online form here.
Source:
Lupus Foundation of America http://www.medicalnewstoday.com/articles/206006.php
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Believe those who are seeking the truth. Doubt those who find it.
Andre Gide
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