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Compassionate Drug Use Group 4 Andrew Nicklawsky, Sarah Cusick, Zequing Lu, Anna Nordell, Jun Park, Pamela Portschy, Dongiuan Xu, Dariya Yegorova DEFINITIONS • Treatment of a seriously ill patient with a new, unapproved drug/procedure/device when no other treatments are available • Legal – first approved in 1987 – Two ways/programs through which patients can access Drugs: • Expanded Access • Single Patient Access EXPANDED ACCESS • Drug in Phase III of clinical trial – patients who were not able to enroll initially, or at all, can access drug • FDA allows Expanded Access if it can demonstrated to work in some capacity • 21 CFR 312.300 (Subpart I) EXPANDED ACCESS (CONT.) • “Expanded access, sometimes called "compassionate use," is the use of an investigational drug outside of a clinical trial to treat a patient with a serious or immediately lifethreatening disease or condition who has no comparable or satisfactory alternative treatment options. “ (www.fda.gov) • The need for expanded access is recognized by patient advocacy groups, physicians, and medical researchers SINGLE PATIENT ACCESS • Patients who did not enter in the clinical trial and were unable to qualify for expanded access may lobby for use of the drug • Doctor must request drug • If company allows use, doctor and company ask for FDA approval JUSTIFICATION • Life-threatening diseases where the patient’s prognosis is extremely poor in the near future • No comparable or satisfactory therapeutic alternatives • Access and administration of the drug is tightly controlled by the FDA and the patient’s physician • Companies are not required to make their drug available through expanded access, or to make more of a drug for that purpose. ARGUMENTS TO SUPPORT EXISTING PROGRAMS WHO BENEFITS: • Patients with the following characteristics may be able to receive drugs that are not yet available on the open market – – – – Advanced disease Established treatments did not work Ineligible for current clinical trials Benefit outweighs the potential risk EXAMPLE • Clinical Trial for Iressa – oral agent with little toxicity • Iressa showed promised in reducing tumors in patients with nonsmall cell lung cancer (75% of lung cancers fall in this category) • 10% of subjects enrolled in trial had dramatic results during Phase I • Opened up to expanded access • 20,000 patients were enrolled who had nonsmall lung cancer and were unresponsive or could not take chemo WHAT ABOUT PATIENT SAFETY? SAFEGUARDS IN PLACE FOR CURRENT PROGRAMS • Tight control and oversight by the FDA and physicians • Companies not obligated to provide the drug • Limited amounts of drug, costly to produce extra SAFEGUARDS (CONT.) • Both the FDA and company need to be in agreement that the drug can be used outside of trial BENEFIT TO RESEARCHERS • Gain a better understanding of the medication it a real world clinical setting • See potential effects/side effects not evident through tightly controlled trials • Generate hypotheses for future trials Conclusion ● Expanded Access Programs provide hope for those who may have none ● Can help to provide additional information on both the positive, and unfortunately, negative effects of experimental medical procedures, drugs, and devices ● Critics often point to the higher number of deaths and adverse events that occur ● Fail to take into account the fact that expanded access programs target population REFERENCES • • • • • http://www.policymed.com/2013/06/fda-expanded-access-toinvestigational-drugs-for-treatment-use-draft-guidance.html http://www.cancer.org/treatment/treatmentsandsideeffects/clini caltrials/compassionate-drug-use https://humansubjects.stanford.edu/research/documents/Expa ndedAccess_GUI01019.pdf http://www.idispharma.com/sites/default/files/uploads/LifeScience-Leader.pdf http://dash.harvard.edu/bitstream/handle/1/8965551/Benjamin %20Rossen%20course%20and%203L%20Paper%20%20Proposed%20Rules%20to%20Expa.pdf?sequence=1 • • • • https://www.nlm.nih.gov/services/ctexpaccess.html http://www.foxnews.com/health/2014/03/26/dying-25-year-oldfights-for-compassionate-use-access-to-cancer-treatment/ https://www.nlm.nih.gov/services/ctexpaccess.html National Academy of Sciences report, 1991 - Expanding access to investigational therapies for HIV infection and AIDS