MedPath

Danoprevir

Generic Name
Danoprevir
Drug Type
Small Molecule
Chemical Formula
C35H46FN5O9S
CAS Number
850876-88-9
Unique Ingredient Identifier
911Z9PCQ5F

Overview

Danoprevir has been used in trials studying the treatment of Hepatitis C, Chronic.

Indication

本品应与利托那韦、聚乙二醇干扰素α和利巴韦林联合组成抗病毒治疗方案,用于治疗初治的非肝硬化的基因1b型慢性丙型肝炎成人患者。

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2017/12/05
Phase 2
Completed
2017/09/20
Phase 1
Completed
2017/01/13
Phase 2
Completed
2017/01/13
Phase 3
Completed
2017/01/13
Phase 1
Completed
2017/01/13
Phase 1
Completed
2017/01/13
Phase 2
Completed
2012/12/13
Phase 2
Completed
2012/10/25
Phase 1
Completed
2012/07/31
Phase 1
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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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