Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea

PHASE2CompletedINTERVENTIONAL
Enrollment

233

Participants

Timeline

Start Date

September 30, 2015

Primary Completion Date

August 31, 2016

Study Completion Date

August 31, 2016

Conditions
RosaceaPapulopustular Rosacea
Interventions
DRUG

FMX-103 1.5%

The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied compared to vehicle in patients with moderate-to-severe papulopustular rosacea. The foam will be applied once daily to the face for the 12-week treatment duration of the study.

DRUG

FMX-103 3%

The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied compared to vehicle in patients with moderate-to-severe papulopustular rosacea. The foam will be applied once daily to the face for the 12-week treatment duration of the study.

DRUG

Vehicle foam (0%)

The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied compared to vehicle in patients with moderate-to-severe papulopustular rosacea. The foam will be applied once daily to the face for the 12-week treatment duration of the study.

Trial Locations (20)

10783

Berlin

13055

Berlin

13086

Berlin

13507

Berlin

15831

Mahlow

21614

Buxtehude

24105

Kiel

40212

Düsseldorf

44803

Bochum

48249

Dülmen

49078

Osnabrück

55131

Mainz

56242

Selters

64283

Darmstadt

70178

Stuttgart

70499

Stuttgart

88045

Friedrichshafen

89081

Ulm

89143

Blaubeuren Abbey

97421

Schweinfurt

All Listed Sponsors
lead

Vyne Therapeutics Inc.

INDUSTRY

NCT02601963 - Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea | Biotech Hunter | Biotech Hunter