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NCT03236233

A Study to Investigate the Safety and Tolerability of Single and Repeat Doses of PC786

Completed Phase 1 Last updated 21 December 2017
What this trial tests

Phase 1 trial testing PC786 - Single doses in Respiratory Syncytial Virus (RSV) in 39 participants. Completed in 15 December 2017.

Timeline
21 June 2017
Primary endpoint
15 December 2017
15 December 2017

Quick facts

Lead sponsorPulmocide Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposetreatment
Enrollment39
Start date21 June 2017
Primary completion15 December 2017
Estimated completion15 December 2017
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Pulmocide Ltd — full company profile →

Who can join

Adults 18 to 65, any sex, with Respiratory Syncytial Virus (RSV). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study investigates the safety, tolerability and pharmacokinetics of single and repeat doses of PC786.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Safety and Antiviral Effects of Nebulized PC786 in a Respiratory Syncytial Virus Challenge Study.
    DeVincenzo J, Cass L, Murray A, Woodward K, et al · · 2022 · cited 38× · PMID 33216113 · DOI 10.1093/infdis/jiaa716
  2. Late therapeutic intervention with a respiratory syncytial virus L-protein polymerase inhibitor, PC786, on respiratory syncytial virus infection in human airway epithelium.
    Brookes DW, Coates M, Allen H, Daly L, et al · · 2018 · cited 31× · PMID 29579332 · DOI 10.1111/bph.14221

Verify or expand the search:

Other recruiting trials for Respiratory Syncytial Virus (RSV)

Currently open trials in the same condition.

Other Pulmocide 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/NCT03236233.

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