Evidence map›Paper›PMID 41416027›Full record

ArticleThe Journal of clinical and aesthetic dermatology2025

Impact of Oral DFD-29, a Low-Dose Formulation of Minocycline, on Quality of Life in Patients with Rosacea: Results of Two Phase 3 Randomized Controlled Trials.

Linda Stein Gold, Paul Yamauchi, Thomas Dirschka, Athanasios Tsianakas, Sunil Dhawan, Srinivas Sidgiddi

2 registry-linked trialsAbstract read
In one paragraph

Article in The Journal of clinical and aesthetic dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05296629 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Parallel-Group, Active and Placebo Controlled Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Extended Release Capsules for the Treatment of Inflammatory Lesions of Rosacea Over 16 Weeks.

TypeinterventionalSponsorJourney Medical CorporationRan2022 to 2023Enrolled323ConditionsPapulopustular RosaceaArmsDFD-29, Doxycycline, Placebo
NCT05343455 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Parallel-Group, Active and Placebo Controlled Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Extended Release Capsules for the Treatment of Inflammatory Lesions of Rosacea Over 16 Weeks

TypeinterventionalSponsorJourney Medical CorporationRan2022 to 2023Enrolled330ConditionsPapulopustular RosaceaArmsDFD-29, Doxycycline, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Linda Stein GoldDr. Stein Gold is with the Henry Ford Health System in Detroit, Michigan.
Paul YamauchiDr. Yamauchi is with the Dermatology Institute and Skin Care Center in Santa Monica, California.
Thomas DirschkaDr. Dirschka is with Centroderm GmbH in Wuppertal, Germany and the University of Witten-Herdecke in Witten, Germany.
Athanasios TsianakasDr. Tsianakas is with Fachklinik Bad Bentheim-Thermalsole-und Schwefelbad Bentheim GmbH in Bad Bentheim, Germany.
Sunil DhawanDr. Dhawan is with the Center for Dermatology Clinical Research, Inc. in Fremont, California.
Srinivas SidgiddiDr. Sidgiddi is with Journey Medical Corporation in Scottsdale, Arizona.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDFD-29 is a low-dose modified formulation of minocycline 40mg that has demonstrated efficacy and safety in patients with rosacea. We report the effect of DFD-29 on patient-reported assessments of disease severity and quality of life (QoL) from two clinical trials in patients with moderate-to-severe rosacea.

methodsMVOR-1 (NCT05296629) and MVOR-2 (NCT05343455) were 16-week, randomized, double-blind, active- and placebo-controlled Phase III trials that compared the impact of oral DFD-29 (EMROSI, Journey Medical Corporation), doxycycline 40mg, and placebo in adults aged 18 years or older with moderate-to-severe rosacea. Changes in QoL were exploratory endpoints that were evaluated at baseline and Weeks 2, 4, 8, 12, and 16 using the Rosacea-Specific Quality of Life (RosaQoL) questionnaire and the Dermatology Life Quality Index (DLQI).

resultsAmong randomized subjects, 288 completed MVOR-1 (DFD-29, n=117; doxycycline, n=98; placebo, n=73) and 296 completed MVOR-2 (DFD-29, n=115; doxycycline, n=113; placebo, n=68). In both trials, DFD-29 significantly improved QoL versus placebo ( LIMITATIONS: RosaQoL and DLQI were exploratory endpoints.

conclusionThese data suggest that DFD-29 may be useful in improving QoL in patients with moderate-to-severe rosacea.

Indexed as

Dermatology Life Quality Index (DLQI)DFD-29doxycyclineminocyclinepatient-reported outcomesquality of lifeRosaceaRosacea-Specific Quality of Life (RosaQoL) questionnaire

Identifiers

PMID41416027
PMCPMC12710994

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.