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Alisertib

Alternative Names: alisertib, mln8237, mln8237 (alisertib)
Latest Update: 2024-12-16
Latest Update Note: Clinical Trial Update

Product Description

A second-generation, orally bioavailable, highly selective small molecule inhibitor of the serine/threonine protein kinase Aurora A kinase with potential antineoplastic activity. Alisertib binds to and inhibits Aurora A kinase, which may result in disruption of the assembly of the mitotic spindle apparatus, disruption of chromosome segregation, and inhibition of cell proliferation. Aurora A kinase localizes to the spindle poles and to spindle microtubules during mitosis, and is thought to regulate spindle assembly. Aberrant expression of Aurora kinases occurs in a wide variety of cancers, including colon and breast cancers. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/alisertib)

Mechanisms of Action: AURK Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Orphan Drug - Lung Cancer|Small Cell Lung Cancer *

Approval Status: Not Approved

Approved Countries: Slovenia

Approved Indications: None

Known Adverse Events: None

Company: Puma Biotechnology
Company Location: LOS ANGELES CA 90024
Company CEO: Alan H. Auerbach
Additonal Commercial Interests: Takeda

Clinical Description

Map of Global Clinical Trials for Alisertib

Countries in Clinic: Portugal, Spain, United States

Active Clinical Trial Count: 4

Highest Development Phases

Phase 2: Breast Cancer|Small Cell Lung Cancer

Phase 1: Lung Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

PUMA-ALI-1201

P2

Unknown Status

Breast Cancer

2029-06-01

ALISCA-Breast1

P2

Recruiting

Breast Cancer

2027-06-30

NCI-2019-05913

P1

Recruiting

Lung Cancer

2026-12-31

ALISCA-Lung1

P2

Recruiting

Small Cell Lung Cancer

2025-07-31

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