People frequently wonder about the safety of
participating in a clinical trial, but for cancer patients, this option is
often the best choice available. Dr. Fernando Rivera, Head of Medical Oncology
at Valdecilla Hospital (Santander, Spain), explains it this way:
“Clinical trials are not only valuable for
society—being the only way to advance cancer treatments and translate basic
scientific discoveries into real benefits for patients—but they also directly
benefit the participants. Patients in clinical trials gain access to
cutting-edge treatments long before they become widely available outside the
trial setting.”
“It’s important to understand that developing a new
cancer drug is a lengthy process. From the initial laboratory studies to the
first use in patients within a clinical trial, it typically takes 3 to 5 years.
Then, from the start of clinical trials through all development phases (I, II,
and III) until the drug is approved for routine use, another 5 to 10 years may
pass.”
“During those years when the drug is still under
investigation, the only way to access it is through a clinical trial. In many
cases, this represents the best therapeutic option we can offer patients.”
Source: Statements by Dr. Fernando Rivera to the
Cantabria College of Physicians
A journey through the history of the pharmaceutical industry and one of its great laboratories that had its origins in Alfred Nobel...
“From Alfred Nobel to AstraZeneca” (Vicente Fisac, Amazon) is available in e-Book and print editions: https://a.co/d/9svRTuI
A journey through the history of the pharmaceutical industry and one of its great laboratories that had its origins in Alfred Nobel...
“From Alfred Nobel to AstraZeneca” (Vicente Fisac, Amazon) is available in e-Book and print editions: https://a.co/d/9svRTuI
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