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NCT00984854

A Trial to Investigate the Clinical Safety, Local Toleration, and Systemic Pharmacokinetics of Repeated, Escalating Concentrations of Intradermal RN1004 to Wounds of Healthy Subjects.

Completed Phase 1 Last updated 24 September 2009
What this trial tests

Phase 1 trial testing Juvidex in Cicatrix in 70 participants. Completed in 1 July 2004.

Timeline
1 January 2004
Primary endpoint
1 July 2004
1 July 2004

Quick facts

Lead sponsorRenovo
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment70
Start date1 January 2004
Primary completion1 July 2004
Estimated completion1 July 2004
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Renovo — full company profile →

Who can join

Adults 18 to 45, any sex, with Cicatrix or Re-epithelialisation. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study was to investigate the safety and toleration of various doses of intradermal Juvidex (mannose-6-phosphate) administered to punch biopsies of normal subjects.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Novel pharmacotherapy for burn wounds: what are the advancements.
    Hamblin MR. · · 2019 · cited 17× · PMID 30517046 · DOI 10.1080/14656566.2018.1551880

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Other recruiting trials for Cicatrix

Currently open trials in the same condition.

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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/NCT00984854.

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