Safety and Efficacy Study of M2951 in Participants With Rheumatoid Arthritis

PHASE2CompletedINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

July 31, 2016

Primary Completion Date

April 30, 2017

Study Completion Date

November 14, 2017

Conditions
Rheumatoid Arthritis
Interventions
DRUG

Placebo

Participants received placebo matched to M2951 twice daily up to Day 84 during the double-blind treatment period.

DRUG

M2951

Participants received 50 milligrams (mg) M2951 orally twice daily up to Day 84 during the double-blind treatment period.

DRUG

M2951

Participants who received placebo matched to M2951 or M2951 in double-blind treatment period, received 50 mg M2951 orally twice daily up to 26-weeks during the open label extension period.

Trial Locations (2)

Unknown

U.S. Medical Information, Billerica

Merck KGaA Communication Center, Darmstadt

All Listed Sponsors
collaborator

Merck KGaA, Darmstadt, Germany

INDUSTRY

lead

EMD Serono Research & Development Institute, Inc.

INDUSTRY

NCT02784106 - Safety and Efficacy Study of M2951 in Participants With Rheumatoid Arthritis | Biotech Hunter | Biotech Hunter