Evidence map›Paper›PMID 42455415›Full record

ArticleTherapeutic innovation & regulatory science2026

FDA Accelerated Approval Disclosures on Direct-to-Consumer Prescription Drug Websites: Testing Presence, Prominence, and Wording.

Helen W Sullivan, Amie C O'Donoghue, Mihaela Johnson

Abstract read
In one paragraph

Article in Therapeutic innovation & regulatory science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Helen W SullivanUS. Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD, 20993, USA. helen.sullivan@fda.hhs.gov.ORCID http://orcid.org/0000-0001-7621-7554
Amie C O'DonoghueUS. Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD, 20993, USA.
Mihaela JohnsonRTI International, Durham, NC, USA.

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

objectivesThe US Food and Drug Administration (FDA) provides a pathway, known as accelerated approval, intended to facilitate and expedite development and review for prescription drugs that treat serious or life-threatening illnesses such as cancer. Many direct-to-consumer websites for accelerated approval prescription drugs include a disclosure describing concepts related to accelerated approval, such as the basis of the approval, uncertainty about clinical benefits of the drug, and the need for confirmatory clinical trials. The current research examined the presence, wording, and prominence of an accelerated approval disclosure on a prescription drug website.

methodsWe conducted two studies with different populations: Study 1 participants were 822 general population US adults. Study 2 participants were 615 US adult cancer patients and caregivers. In each study, we randomly assigned participants to view one of five versions of a website for a fictitious acute lymphoblastic leukemia prescription drug. The control website did not include the disclosure about accelerated approval. The four disclosure conditions varied by disclosure prominence (low vs. high) and disclosure wording (consumer-friendly vs. based on the physician labeling and disclosures in the real-world marketplace).

resultsIn comparison to a disclosure based on physician labeling, a consumer-friendly disclosure helped participants understand accelerated approval concepts. For example, more participants in the consumer-friendly disclosure than in the physician-labeling disclosure condition knew the drug has not been shown to help patients live longer (Study 1: 13.4% vs. 31.4%; Study 2: 12.2% vs. 34.4%). Comparisons with the control condition demonstrated that while including either the physician-labeling or consumer-friendly disclosure increased participants' awareness of the disclosure, only the presence of the consumer-friendly disclosure improved comprehension of accelerated approval concepts. There were few effects for increasing prominence of the disclosure.

conclusionsAdding a consumer-friendly disclosure to promotional websites may help consumers, patients, and caregivers understand a prescription drug's accelerated approval status.

Indexed as

Accelerated approvalCaregiverComprehensionDirect-to-consumerDisclosurePatientPrescription drug

Identifiers

PMID42455415
PMCPMC13384201

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.