MedPath

Lucitanib

Generic Name
Lucitanib
Drug Type
Small Molecule
Chemical Formula
C26H25N3O4
CAS Number
1058137-23-7
Unique Ingredient Identifier
PP449XA4BH

Overview

Lucitanib has been used in trials studying the treatment of ER+, MBC, SCLC, HER2+, and NSCLC, among others.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2020/02/05
Phase 2
UNKNOWN
Haihe Biopharma Co., Ltd.
2019/11/05
Phase 1
Withdrawn
2019/08/01
Phase 1
Suspended
2019/06/20
Phase 1
Terminated
2017/08/24
Phase 1
UNKNOWN
Haihe Biopharma Co., Ltd.
2017/04/17
Phase 1
Completed
Haihe Biopharma Co., Ltd.
2016/04/22
Phase 2
Withdrawn
Teresa Helsten, MD
2014/07/29
Phase 2
Terminated
2014/04/09
Phase 2
Terminated
2014/02/04
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

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