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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
Danoprevir Sodium Tablets
国药准字H20180008
化学药品
片剂
1/18/2023

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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