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Uprosertib

Alternative Names: uprosertib, gsk2141795
Latest Update: 2024-05-15
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: Akt Inhibitor

Novel Mechanism: No

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: GlaxoSmithKline
Company Location: BRENTFORD MIDDLESEX X0 TW8 9GS
Company CEO: Emma Walmsley
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Uprosertib

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Uterine Cancer|Cervical Cancer|Multiple Myeloma|Melanoma|Acute Myeloid Leukemia|Triple Negative Breast Cancer

Phase 1: Triple Negative Breast Cancer|Endometrial Cancer|Melanoma|Ovarian Cancer|Lymphoma|Breast Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCI-2013-02148

P2

Completed

Multiple Myeloma

2019-08-31

NCI-2013-01320

P2

Active, not recruiting

Melanoma

2018-05-16

NCT01958112

P2

Terminated

Uterine Cancer|Cervical Cancer

2017-11-01

NCI-2013-01895

P2

Completed

Triple Negative Breast Cancer

2017-01-20

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