‘Free WCG Foundation webinars offer insights on speeding access to experimental drugs for intermediate-size patient populations
Presenters include Richard Klein, formerly of FDA, and Marjorie Speers of WCGF
ATLANTA, Ga., Jan. 9, 2018—WCG Foundation will host free webinars Jan. 25 and Feb. 5 on how to streamline the application process for experimental medications for intermediate-size populations of desperately ill patients.
The webinars—“Intermediate-Size Patient Populations INDs: What Are They, When Should They Be Used, and Who May Apply for Them?”—feature Richard Klein, former director of the Food and Drug Administration Patient Liaison Program Office, and Marjorie A. Speers, Ph.D., executive director, WCGF.
‘Right to Try Bills Push the Needle on Risk’ – panel of experts, including WCGF Executive Director Marjorie A. Speers, discuss risks associated with Right-to-Try legislation
Published December 24, 2017 by OncLive
“Congressional “right-to-try” legislation could make investigational drugs available to desperately ill patients sooner in the trials process, but there are substantial risks, said a panel of experts at the Patient-Centered Oncology Conference, held November 16-17 in Philadelphia, Pennsylvania.
Earlier in the clinical trials process, less is known about the drugs, which may be highly toxic and may have no efficacy. Furthermore, the House of Representatives’ version of the bill would allow companies to charge any amount for access to their investigational drugs. That is a scary proposition due to the potential for cost exploitation, members of the panel said.”
You can read the full article from OncLive HERE
Panel of experts, including WCGF Executive Director Marjorie A. Speers, discuss Right to Try bill at Patient Centered Oncology Care 2017 meeting
Published November 17, 2017 by HCA News
“Marjorie A. Speers, Executive Director of the WCG Foundation, also had problems with Right to Try laws. Under the existing system, the process encourages deliberate decisions: first, the patient and their physician decide they want to pursue a drug undergoing clinical trial; then, they request that access from the drug’s maker and the company can decide if they believe the drug will be useful; finally, the FDA reviews and approves the request.
Right to Try, Speers argued, bypasses all of that, which could be detrimental. “These uses can only occur for desperately ill people, there’s no other treatment option for them,” she said. “It’s not necessarily the best time to be making a decision.”’
You can read the full article from Healthcare Analytics News HERE
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WCGF Director David Farber, JD provides expertise in NPR’s 1A Discussion of Expanded Access and Senate Right-To-Try Legislation
David Farber, Partner in the FDA and Life Sciences practice of the law firm King and Spalding, and a Director of WCGF lent his expertise to a nuanced discussion of the questions surrounding expanded access to experimental drugs for patients seeking drugs outside of clinical trials. The program, which provided multiple views on state Right-To-Try legislation as well as the Senate’s recent passing of federal Right to Try legislation, aired on NPR’s 1A program on August 7, 2017.
You can listen to the complete program at:
Pfizer Grant Helps WCG Foundation Identify Obstacles to Expanded Access
WCG Foundation Progress Report, January 25, 2017
WCG Foundation (WCGF) has received a $5,000 grant from Pfizer to identify obstacles that could discourage physicians from helping desperately ill patients who want to access investigational drugs.
The grant is the latest to support WCGF’s Expanded Access Project, which helps those who have exhausted all treatment and clinical trial options and want the chance to try experimental medicines. Learn more.
GlaxoSmithKline Grant Supports WCGF Expanded Access Project
WCG Foundation Progress Report, January 24, 2017
WCG Foundation (WCGF) has received $15,000 from GlaxoSmithKline (GSK) for the Foundation’s Expanded Access Project. The project helps desperately ill patients who have exhausted all treatment and clinical trial options and want to try experimental medicines.
WCGF will use the GSK grant to help institutional review boards (IRB) streamline the process that patients must navigate to gain access to investigational drugs and devices. Learn more.
$100,000 Grant from Robert Wood Johnson Foundation Supports WCGF Expanded Access Program
WCG Foundation Progress Report, October 31, 2016
WCG Foundation (WCGF) has received $100,000 from the Robert Wood Johnson Foundation (RWJF) to support WCGF’s new Expanded Access Project. The grant targets physicians and institutional review boards (IRBs), who play key roles in helping desperately ill patients gain access to experimental medicines.
Launched in July, the Expanded Access Project seeks to streamline the process for those seeking Food and Drug Administration (FDA) approval to try investigational drugs and devices. The goal is to make the process less burdensome and more equitable and transparent. Learn more.
First WCGF Grant Funds Innovative Research Ethics Curriculum at NYU
WCG Foundation Progress Report, August 17, 2016
WCG Foundation’s (WCGF’s) first grant—a two-year $200,000 award to New York University (NYU)—has already enabled NYU Langone Medical Center (NYULMC) to strengthen research ethics education within and beyond the medical center. During the first year, NYU funded curriculum development and supported faculty participation in lectures, webinars, panel discussions, and other outreach efforts.
As a result, 20 students at NYULMC completed a new course in research ethics and integrity, and 12 research professionals from resource-poor countries attended a two-week intensive ethics training program. In addition, thousands of students and faculty from the nation’s top academic institutions and high schools gained a better understanding of today’s research ethics issues through webinars, lectures, and publications. Learn more.
Foundation Seeks IRBs to Review Single-Patient Expanded Access Applications
WCG Foundation RFP, July 28, 2016
WCG Foundation (WCGF) has issued a request for proposals (RFP) to pilot an expanded access program. The Foundation wishes to engage several organizations with institutional review boards (IRBs) to conduct full board reviews of single-patient expanded access (compassionate use) applications. Details are available in the RFP.
Deadline to respond is 5 p.m. EDT August 29.