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Crisaborole

Alternative Names: crisaborole, an2728, Eucrisa
Latest Update: 2024-11-13
Latest Update Note: News Article

Product Description

Crisaborole is used to treat eczema (atopic dermatitis; a skin condition which causes the skin to be dry and itchy and to sometimes develop red, scaly rashes) in adults and children 3 years of age and older. Crisaborole is in a class of medications called phosphodiesterase inhibitors. It works by blocking the action of certain natural substances in the body that cause inflammation. (Sourced from: https://medlineplus.gov/druginfo/meds/a617019.html)

Mechanisms of Action: PDE4 Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Topical

FDA Designation: None *

Approval Status: Approved

Approved Countries: Argentina | Australia | Austria | Bangladesh | Belgium | Canada | Croatia | Egypt | European Medicines Agency | Finland | Greece | Hong Kong | Hungary | Iceland | India | Ireland | Israel | Italy | Latvia | Lebanon | Lithuania | Mexico | Poland | Portugal | Saudi Arabia | South Africa | Sweden | Taiwan | United Arab Emirates | United States | Uruguay

Approved Indications: Dermatitis | Dermatitis, Atopic

Known Adverse Events: Pain Unspecified

Company: Pfizer
Company Location: NEW YORK NY 10017
Company CEO: Albert Bourla
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Crisaborole

Countries in Clinic: Australia, Canada, China, Israel, Turkey, United States

Active Clinical Trial Count: 9

Highest Development Phases

Phase 3: Dermatitis, Atopic

Phase 2: Vitiligo

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCT05298033

P2

Completed

Vitiligo

2024-04-30

CrisADe Control

P3

Completed

Dermatitis, Atopic

2022-12-27

NCT04800185

P1

Completed

Dermatitis, Atopic

2022-04-30

C3291035

P3

Completed

Dermatitis, Atopic

2022-01-19

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