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NK-012

Alternative Names: nk-012, nk012, nk 012
Latest Update: 2018-11-07
Latest Update Note: Clinical Trial Update

Product Description

Nippon Kayaku was developing nk-012, an intravenous TOP Inhibitor,DNA Synthesis Inhibitor for advanced solid tumors. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT01238952)

Mechanisms of Action: TOP Inhibitor,DNA Synthesis Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Nippon Kayaku
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NK-012

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Multiple Myeloma|Small Cell Lung Cancer|Triple Negative Breast Cancer|Colorectal Cancer

Phase 1: Colorectal Cancer|Triple Negative Breast Cancer|Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

A6012211US

P2

Completed

Triple Negative Breast Cancer

2014-12-01

JapicCTI-111652

P2

Completed

Multiple Myeloma

2014-09-01

A6012113US

P1

Completed

Colorectal Cancer

2013-12-01

A6012212US

P2

Completed

Small Cell Lung Cancer

2012-01-01

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