Incorporating patient perspectives into drug development seems like a no-brainer, but it's not always easy. Stumbling blocks remain despite recent efforts to involve patients and their caregivers in clinical trial design and regulatory processes, speakers noted in a June 8 panel discussion during the Biotechnology Innovation Organization (BIO) International Convention in San Francisco.
Case in point: Sarepta Therapeutics Inc. has been accused of using Duchenne muscular dystrophy (DMD) patients and their families...
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