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NCT02460016

A Study of AK0529 in Infants Hospitalized With RSV

Terminated Phase 1 Last updated 2 July 2018
What this trial tests

Phase 1 trial testing AK0529 in Respiratory Syncytial Virus Infections in 1 participant. Terminated before completion.

Timeline
28 August 2015
Primary endpoint
3 November 2015
3 November 2015

Quick facts

Lead sponsorShanghai Ark Biopharmaceutical Co., Ltd.
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment1
Start date28 August 2015
Primary completion3 November 2015
Estimated completion3 November 2015
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Ark Biopharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 1 Month to 24 Months, any sex, with Respiratory Syncytial Virus Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will assess the safety, tolerability, pharmacokinetics (PK) and anti-viral effect of single dose of AK0529 in infants hospitalized with respiratory syncytial virus (RSV).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of AK0529

Trials testing the same drug.

Other recruiting trials for Respiratory Syncytial Virus Infections

Currently open trials in the same condition.

Other Shanghai Ark Biopharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02460016.

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