Blocking Interferon-γ by Ruxolitinib for Treating Inclusion Body Myositis: a Phase IIb Trial

Status: Recruiting
Location: See all (16) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Refer to the Detailed Description section.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Healthy Volunteers: f
View:

• Age ≥ 45 years

• Effective contraception for the duration of the clinical trial for fertile women of childbearing age

• Defined diagnosis of IBM according to data-derived criteria (Llyod et al, 2014): Patient must fulfill the three following criteria for being diagnosed as IBM: (1) finger flexor or quadriceps weakness; and (2) muscle biopsy showing endomysial inflammation; and (3) muscle biopsy showing invasion of nonnecrotic muscle fibers or rimmed vacuoles

• To be able to walk 6 min without assistance from another person (external assist devices permitted \[e.g., canes, walkers, or rollators\])

• Patient informed and having signed the consent for participation, possibly assisted by a trusted person

Locations
Other Locations
France
Hôpital Pellegrin - Tripode, CHU de Bordeaux
ACTIVE_NOT_RECRUITING
Bordeaux
Hôpital Pierre Wertheimer, CHU de Lyon
ACTIVE_NOT_RECRUITING
Bron
CHU Caen Normandie
ACTIVE_NOT_RECRUITING
Caen
Hôpital Henri-Mondor, APHP
RECRUITING
Créteil
Hôpital Raymond Poincaré, APHP
ACTIVE_NOT_RECRUITING
Garches
Hôpital Roger Salengro, CHU de Lille
NOT_YET_RECRUITING
Lille
Hôpital Dupuytren, CHU de Limoges
ACTIVE_NOT_RECRUITING
Limoges
Hôpital de la Timone, APHM
NOT_YET_RECRUITING
Marseille
CHU Nancy
ACTIVE_NOT_RECRUITING
Nancy
Hôtel-Dieu, CHU Nantes
NOT_YET_RECRUITING
Nantes
Hôpital Pasteur, CHU de Nice
RECRUITING
Nice
Hôpital Pitié-Salpêtrière, APHP
ACTIVE_NOT_RECRUITING
Paris
Hôpital Christian Cabrol, CHU Reims
ACTIVE_NOT_RECRUITING
Reims
Hôpital Bellevue, CHU Saint-Etienne
ACTIVE_NOT_RECRUITING
Saint-etienne
Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg
NOT_YET_RECRUITING
Strasbourg
Hôpital Pierre-Paul Riquet, CHU de Toulouse
NOT_YET_RECRUITING
Toulouse
Contact Information
Primary
François Jérôme AUTHIER, Pr
francois-jerome.authier@aphp.fr
+33 1 4981 2735
Time Frame
Start Date: 2025-05-27
Estimated Completion Date: 2028-09-10
Participants
Target number of participants: 80
Treatments
Experimental: Experimental group
Randomization in experimental group.
Placebo_comparator: Control group
Randomization in control group.
Related Therapeutic Areas
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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