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NCT03780465

A Study of Safety and Tolerability of NOX66 in Healthy Volunteers

Withdrawn Phase 1 Last updated 28 May 2019
What this trial tests

Phase 1 trial testing Oral idronoxil suspension in Healthy Volunteers. Withdrawn.

Timeline
1 March 2019
Primary endpoint
1 March 2019
1 March 2019

Quick facts

Lead sponsorNoxopharm Limited
PhasePhase 1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingtriple
Primary purposetreatment
Start date1 March 2019
Primary completion1 March 2019
Estimated completion1 March 2019
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Noxopharm Limited — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A Phase 1, double- blinded, randomised, placebo-controlled study to assess safety, tolerability and pharmacokinetics of 2 formulations of NOX66 in healthy subjects when administered over 4 cohorts as single NOX66 dose of 400 mg and 600 mg in comparison to single oral dose of 400 mg idronoxil.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Healthy Volunteers

Currently open trials in the same condition.

Other Noxopharm Limited 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/NCT03780465.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing