During initial clinical trials of the novel medication Xylofen, every participant possessing the genetic mutation K-22 experienced a complete cessation of migraine symptoms within hours of administration. Participants lacking the K-22 mutation exhibited highly variable responses in the clinical trials, with some experiencing complete cessation and others reporting no effect. The K-22 mutation is present in precisely of the general population who suffer from migraines. When Xylofen was approved and introduced into general medical practice, physicians prescribed it to migraine sufferers without testing for the K-22 mutation, resulting in the drug being distributed to patients with and without the mutation in exact proportion to their representation in the migraine-suffering population. Nevertheless, data from the first year of general practice showed that only of all patients prescribed Xylofen experienced a complete cessation of symptoms within hours.
Which of the following is most strongly supported by the information above?
- AThe failure of Xylofen to produce complete symptom cessation in the vast majority of general practice patients was due to differences in the demographic composition between the trial participants and the general population.
- BThe absolute number of patients without the K-22 mutation who experienced a complete cessation of symptoms in general medical practice was greater than the number of patients with the K-22 mutation who experienced such a cessation.
- CIn general medical practice, a majority of the patients who experienced a complete cessation of symptoms within hours were individuals who possessed the K-22 mutation.
- Among patients who possess the K-22 mutation and were prescribed Xylofen, the proportion who experienced a complete cessation of symptoms within hours was lower in general medical practice than it was during the initial clinical trials.Answer
- EIn the initial clinical trials, any participant who experienced a complete cessation of migraine symptoms within hours was guaranteed to possess the K-22 mutation.