Ozmosi | NK-012 Drug Profile
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NK-012

Alternative Names: nk-012, nk012, nk 012
Clinical Status: Inactive
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: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

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

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

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

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

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01238939

A6012113US

P1

Completed

Colorectal Cancer

2013-12-01

2019-03-19

Treatments

NCT01238952

A6012121US

P1

Completed

Triple Negative Breast Cancer

2010-11-01

2019-03-19

Treatments

NCT00542958

N06-10089

P1

Completed

Oncology Solid Tumor Unspecified

2008-04-01

2019-03-21

Treatments

NCT00951054

A6012211US

P2

Completed

Triple Negative Breast Cancer

2014-12-01

2019-03-18

Treatments

JapicCTI-111652

JapicCTI-111652

P2

Completed

Multiple Myeloma

2014-09-01

NCT00951613

A6012212US

P2

Completed

Small Cell Lung Cancer

2012-01-01

2019-03-18

Treatments

JapicCTI-090780

JapicCTI-090780

P2

Completed

Colorectal Cancer

None

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