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FDA approval, clinical trial evidence, efficacy, epidemiology, and price for non-orphan and ultra-ra...

FDA approval, clinical trial evidence, efficacy, epidemiology, and price for non-orphan and ultra-ra...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2811941786

FDA approval, clinical trial evidence, efficacy, epidemiology, and price for non-orphan and ultra-rare, rare, and common orphan cancer drug indications: cross sectional analysis

About this item

Full title

FDA approval, clinical trial evidence, efficacy, epidemiology, and price for non-orphan and ultra-rare, rare, and common orphan cancer drug indications: cross sectional analysis

Publisher

England: British Medical Journal Publishing Group

Journal title

BMJ (Online), 2023-05, Vol.381, p.e073242

Language

English

Formats

Publication information

Publisher

England: British Medical Journal Publishing Group

More information

Scope and Contents

Contents

AbstractObjectiveTo analyze the US Food and Drug Administration (FDA) approval, trials, unmet needs, benefit, and pricing of ultra-rare (<6600 affected US citizens), rare (6600-200 000 citizens), and common (>200 000 citizens) orphan cancer drug indications and non-orphan cancer drug indications.DesignCross sectional analysis.SettingData from Drugs...

Alternative Titles

Full title

FDA approval, clinical trial evidence, efficacy, epidemiology, and price for non-orphan and ultra-rare, rare, and common orphan cancer drug indications: cross sectional analysis

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2811941786

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2811941786

Other Identifiers

ISSN

1756-1833

E-ISSN

1756-1833

DOI

10.1136/bmj-2022-073242

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