Efficacy of an Adapted Antibiotherapy in Hurley Stage 2 Hidradenitis Suppurativa Patients

PHASE3RecruitingINTERVENTIONAL
Enrollment

92

Participants

Timeline

Start Date

May 22, 2025

Primary Completion Date

February 28, 2027

Study Completion Date

February 27, 2028

Conditions
Hidradenitis Suppurativa
Interventions
DRUG

ROCEPHIN, metronidazole, RIFADIN, IZILOX, placebo combination therapy

a 3-week course of ceftriaxone injection + oral metronidazole followed by a 3-week course of oral rifampicin + moxifloxacin +metronidazole followed by a 6-week course of oral rifampicin + moxifloxacin

DRUG

Lymecyclin and corresponding placebos of the experimental arm

12-week course of oral lymecycline.

Trial Locations (4)

Unknown

NOT_YET_RECRUITING

Hôpital de la Timone, Marseille

RECRUITING

Centre Médical de l'Institut Pasteur, Paris

ACTIVE_NOT_RECRUITING

Hopital St Joseph, Paris

NOT_YET_RECRUITING

CHU de Rouen, Rouen

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Centre Hospitalier Universitaire de Caen

OTHER

collaborator

Hôpital Necker-Enfants Malades

OTHER

collaborator

Ministry of Health, France

OTHER_GOV

collaborator

Assistance Publique Hopitaux De Marseille

OTHER

lead

Institut Pasteur

INDUSTRY

NCT05821478 - Efficacy of an Adapted Antibiotherapy in Hurley Stage 2 Hidradenitis Suppurativa Patients | Biotech Hunter | Biotech Hunter