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NCT03667222: PRISM

Topical Minocycline Gel for Inflammatory Lesions of Papulopustular Rosacea

Status unknown Phase 2 Last updated 10 July 2019
What this trial tests

Phase 2 trial testing minocycline topical gel in Papulopustular Rosacea in 207 participants. Status unknown.

Timeline
18 September 2018
Primary endpoint
17 May 2019
17 August 2019

Quick facts

Lead sponsorBioPharmX, Inc.
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment207
Start date18 September 2018
Primary completion17 May 2019
Estimated completion17 August 2019
Sites12 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

BioPharmX, Inc. — full company profile →

Who can join

18 and older, any sex, with Papulopustular Rosacea. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a 12-week, multicenter, double-blind, randomized, two-arm, vehicle controlled study. Subjects will be randomized 1:1 to BPX-04 minocycline topical gel 1% or vehicle. This study will include approximately 176 randomized subjects with inflammatory lesions of papulopustular rosacea on the face, defined by an IGA score of 3 (moderate) or 4 (severe) at Baseline. Subjects will be healthy male or female subjects aged 18 years or older. There will be up to 20 study sites in the USA.

Publications & conference data

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

  1. A Review of Systemic Minocycline Side Effects and Topical Minocycline as a Safer Alternative for Treating Acne and Rosacea.
    Martins AM, Marto JM, Johnson JL, Graber EM. · · 2021 · cited 48× · PMID 34206485 · DOI 10.3390/antibiotics10070757

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Other recruiting trials for Papulopustular Rosacea

Currently open trials in the same condition.

Other BioPharmX, Inc. trials

Trials by the same sponsor.

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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/NCT03667222.

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