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PI3K inhibitor BYL719

Vanderbilt-Ingram Cancer Center · Phase 1 active Small molecule Quality 20/100

PI3K inhibitor BYL719 is a Small molecule drug developed by Vanderbilt-Ingram Cancer Center. It is currently in Phase 1 development. Also known as: BYL719, a-specific phosphoinositide 3-kinase inhibitor BYL719, BYL719, phosphoinositide 3-kinase inhibitor BYL719.

At a glance

Generic namePI3K inhibitor BYL719
Also known asBYL719, a-specific phosphoinositide 3-kinase inhibitor BYL719, BYL719, phosphoinositide 3-kinase inhibitor BYL719
SponsorVanderbilt-Ingram Cancer Center
ModalitySmall molecule
PhasePhase 1

Approved indications

No approved indications tracked.

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about PI3K inhibitor BYL719

What is PI3K inhibitor BYL719?

PI3K inhibitor BYL719 is a Small molecule drug developed by Vanderbilt-Ingram Cancer Center.

Who makes PI3K inhibitor BYL719?

PI3K inhibitor BYL719 is developed by Vanderbilt-Ingram Cancer Center (see full Vanderbilt-Ingram Cancer Center pipeline at /company/vanderbilt-ingram-cancer-center).

Is PI3K inhibitor BYL719 also known as anything else?

PI3K inhibitor BYL719 is also known as BYL719, a-specific phosphoinositide 3-kinase inhibitor BYL719, BYL719, phosphoinositide 3-kinase inhibitor BYL719.

What development phase is PI3K inhibitor BYL719 in?

PI3K inhibitor BYL719 is in Phase 1.

What are the side effects of PI3K inhibitor BYL719?

Common side effects of PI3K inhibitor BYL719 include Aspartate Aminotransferase Increased, Hyperglycemia, Peripheral Sensory Neuropathy, Anemia, Fatigue, Alkaline Phosphatase Increased.

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