The US Food and Drug Administration (FDA) initiated the accelerated approval pathway in 1992 in response to the HIV epidemic as a way to expedite clinical trial evaluations of promising drugs in the treatment of serious or life-threatening disease. The accelerated approval pathway explicitly allows biomarkers to be used as primary efficacy end points and permits those biomarkers to be only "reasonably likely" to predict clinical benefit. When a drug receives accelerated approval, there is usually lesser certainty of clinical benefit than if approval were based on clinical outcomes, such as improvements in how a patient feels or functions or prolonged survival. In contrast, the FDA's regular approval pathway is typically based on clinical outcomes, although in recent years the agency has permitted the use of surrogate markers for clinical benefit with increasing frequency. 1 Because clinical benefits have not been demonstrated for drugs that receive accelerated approval, postapproval studies are required by law. If these studies do not confirm the benefit of the drug, the approval is supposed to be withdrawn, either voluntarily by the sponsor or by the FDA revoking the approval. In theory, accelerated approval strikes a balance between access to therapies for life-threatening diseases based on promising data and the need for convincing evidence demonstrating that these therapies improve patients' lives. At present, the accelerated approval pathway is commonly used, particularly for cancer therapies; in 2017, 40% of cancer drugs for treatment of solid tumors in adults received such approvals. 1 In 2021, there has been controversy about the accelerated approval pathway in 2 high-profile contexts. First, some cancer drugs with accelerated approval failed their confirmatory trials but were not voluntarily withdrawn from the market, as discussed at an FDA Oncologic Drugs Advisory Committee (ODAC) meeting in April 2021. Then, in June 2021, the FDA used the accelerated approval pathway for aducanumab (Aduhelm, Biogen) for Alzheimer disease, based on the drug's ability to decrease the number of visible amyloid plaques in the brain. 2 The oncology drugs that failed their confirmatory trials and the approval of aducanumab highlight 3 key concerns about the accelerated approval pathway. First, approval of aducanumab demonstrated a lack of consistency about what it means for a surrogate measure to be "reasonably likely" to predict clinical benefit. Amyloid plaques, which are often but not always visible in patients with Alzheimer disease, previously have been targeted by several drugs without evidence of improving cognitive function. These findings call into question the