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Living With Cancer

Advocacy

Compassionate Use Overview

A patient with:

  • advanced disease
  • no approved treatment options
  • no appropriate clinical trial options

may consider trying to get a new, unapproved drug outside of the clinical trial.

Access to a scientifically-tested drug outside of a clinical trial and prior to FDA approval has many names but is most commonly referred to as compassionate use.

When a drug company decides to provide access to their unapproved drug outside of the clinical trial they most commonly do it in the following two ways:

Expanded Access Programs (EAP)

Drug companies in the late stages of drug development including the Phase III clinical trial stage, can offer Expanded Access Programs for patients who are not able to enroll in a clinical trial. The FDA generally approves these programs if the drug has demonstrated some effectiveness against a specific cancer in the on-going clinical trials.

Single Patient Access

Patients who are not eligible for either clinical trials or an Expanded Access Program (if one exists) may be eligible to receive the unapproved new drug by applying for Single Patient Access. In this situation, the patient's doctor must first request permission for access to the drug from the drug company. If the company agrees, the patient's doctor works with the drug company to apply for FDA approval for use of the drug for the patient. The timeline for Single Patient Access varies. In an emergency, the FDA can walk the paperwork through in 24 hours.

Check Meeting FDA Requirements for Single Patient Access for more details on the Single Patient Access process.

Cautionary Notes

  • Prepare to be confused: There are several regulatory mechanisms (programs) along with multiple terms and definitions that are used to describe how a patient may get access to an unapproved new drug outside of a clinical trial. We will define terms used on this web site but we want you to understand that drug companies, patient advocacy organizations and the FDA may use different terms.

For example, the FDA terminology is specified in the FDA regulations. Most drug companies refer to their compassionate access programs with terms that are unique to their specific program and inconsistent with the FDA language. In short, the definitions and terms can be confusing.

  • The simplest way to get access to an unapproved drug is through a clinical trial. Expanded access programs, if offered by the drug company, offer another option. If neither of those two options exists, access through single-patient compassionate use may be possible.
  • Working out single-patient compassionate use of an unapproved drug will be confusing, time-consuming and frustrating. There is no single policy or process adhered to by the FDA and drug companies. There is no single list of drugs currently available through compassionate use. There is no way to force the drug company or FDA to permit treatment through compassionate use.

Drug Company and FDA Approval Required for Compassionate Use

Before a patient or group of patients is allowed to have access to an unapproved, new drug outside of a clinical trial two things MUST be in place:

  • The owner (sometimes referred to as the sponsor, generally a drug company) of the new, unapproved drug must agree to allow the use of their drug outside of the clinical trial, and
  • The FDA oncology medical officer in charge of the regulatory oversight of that new drug's development must concur before the patient or patients may begin taking the drug.

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