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XL-102

Alternative Names: xl-102, xl 102, xl102, AUR-102, AUR102, AUR 102
Latest Update: 2024-05-14
Latest Update Note: Clinical Trial Update

Product Description

XL102 is a potent, selective and orally bioavailable covalent inhibitor of CDK7, which is an important regulator of the cellular transcriptional and cell cycle machinery.

Mechanisms of Action: CDK7 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Exelixis
Company Location: ALAMEDA CA 94502
Company CEO: Michael M. Morrissey
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for XL-102

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Prostate Cancer|Ovarian Cancer|Triple Negative Breast Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

QUARTZ-101

P1

Terminated

Prostate Cancer|Triple Negative Breast Cancer|Ovarian Cancer

2024-05-02

50%

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