Danoprevir

A hepatitis C virus protease inhibitor.

Phase of research

Potential treatment - clinical evidence

How it helps

Antiviral

Drug status

Used to treat other disease

3
Supporting references
0
Contradictory references
7
AI-suggested references
2
Clinical trials

General information

Danoprevir is an experimental anti-hepatitis C virus drug (DrugBank).


Danoprevir on PubChem
Danoprevir on Wikipedia

 

Structure image - Danoprevir

CC(C)(C)OC(=O)N[C@H]1CCCCC/C=C\[C@@H]2C[C@]2(NC(=O)[C@@H]3C[C@H](CN3C1=O)OC(=O)N4CC5=C(C4)C(=CC=C5)F)C(=O)NS(=O)(=O)C6CC6


Supporting references

AI-suggested references

Clinical trials

ID Title Status Phase Start date Completion date
NCT04291729 Evaluation of Ganovo (Danoprevir ) Combined With Ritonavir in the Treatment of SARS-CoV-2 Infection Completed Phase 4 Feb/17/2020 Mar/19/2020
  • Alternative id - ASC-CTP-NC-01
  • Interventions - Drug: Ganovo+ritonavir+/-Interferon nebulization
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - The Ninth Hospital of Nanchang, Nanchang, Jiangxi, China
  • Study designs - Allocation: N/A|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
  • Enrollment - 11
  • Age - 18 Years to 75 Years   (Adult, Older Adult)
  • Outcome measures - Rate of composite adverse outcomes|Time to recovery|Rate of no fever|Rate of no cough|Rate of no dyspnea|Rate of no requiring supplemental oxygen|Rate of undetectable New coronavirus pathogen nucleic acid|Rate of mechanical ventilation|Rate of ICU admission|Rate of serious adverse event
NCT04345276 Efficacy and Safety of Ganovo (Danoprevir) Combined With Ritonavir in the Treatment of SARS-CoV-2 Infection Completed Phase 4 Mar/18/2020 Apr/15/2020
  • Alternative id - ASC-CTP-HS-01
  • Interventions - Drug: Danoprevir+Ritonavir
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Huoshenshan Hostipal, Wuhan, Hubei, China
  • Study designs - Allocation: N/A|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
  • Enrollment - 10
  • Age - 18 Years to 75 Years   (Adult, Older Adult)
  • Outcome measures - Rate of composite adverse outcomes|Time to recovery|Rate of no fever|Rate of no cough|Rate of no dyspnea|Rate of no requiring supplemental oxygen|Rate of undetectable New coronavirus pathogen nucleic acid|Rate of mechanical ventilation|Rate of ICU admission|Rate of serious adverse event