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Completed

NCT Number: NCT01010581

SC12267 (4SC-101) in Combination With Methotrexate in Patients With Rheumatoid Arthritis

The purpose of the study is to determine the efficacy, safety and pharmacokinetics of SC12267 (4SC-101, 35 mg) in combination with methotrexate in comparison to methotrexate alone in the treatment of patients suffering from Rheumatoid Arthritis.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

MHAT "Kaspela" Department of Rheumatology, Plovdiv, Bulgaria

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Main Inclusion Criteria:

  • Patients with active RA of functional classes I, II or III according to the criteria of American Rheumatism Association for RA
  • DAS28(ESR) ≥ 4.5 (DAS28 formula with 4 variables using ESR)
  • Patients who have received weekly doses of MTX (10-25 mg/week) for a minimum of 3 months prior to Day 1 dosing, and who have received a stable MTX dose of 10-25 mg/week without any change in route or change in folic acid supplementation for at least 6 weeks prior to Day 1 dosing
  • Patients may receive up to 10 mg/day of oral prednisolone or steroid equivalent. Dose must have been stable for at least 30 days and must not be changed during the washout, screening and treatment periods, unless dictated by tolerability requirements

Main Exclusion Criteria:

  • Patients with RA of functional classes IV according to the criteria of American Rheumatism Association for RA
  • Patients who have received any of the following treatments must abide by the indicated washout period:
  • Leflunomide requires a 6 month washout period prior to Day 1 dosing
  • Oral or injectable gold, azathioprine, penicillamine, anakinra require a 30 day washout period prior to Day 1 dosing
  • Cyclosporine, abatacept, etanercept, adalimumab, infliximab, and rituximab require a 60 day washout period prior to Day 1 dosing
  • Cyclophosphamide requires a 180 day washout period prior to Day 1 dosing
  • Parenteral or intra-articular corticosteroids require a 30 day washout period prior to Day 1 dosing
  • Receipt of the following drugs within 4 weeks prior to dosing:
  • Sulfasalazine
  • Hydroxychloroquine
  • Use of corticosteroids > 10 mg/day

Treatment and study plan

SC12267 (4SC-101)

Drug

oral administration

Placebo

Drug

oral administration

methotrexate

Drug

oral administration

Folic Acid

Drug

oral administration

Primary outcomes

  1. Efficacy of SC12267 (4SC-101) in combination with methotrexate in patients with RA

    Time frame: 13 weeks

Secondary outcomes

  1. Evaluation of the safety of the combination of SC12267 (4SC-101) and methotrexate in patients with RA

    Time frame: 13 weeks

  2. Evaluation of the plasma concentration (trough value) of SC12267 (4SC-101) after once daily application in combination with methotrexate after once weekly administration.

    Time frame: 13 weeks

Sponsors and collaborators

Lead sponsor

4SC AG

Industry

Registry information

Official study title

A Randomized, Double Blind, Placebo-Controlled, Phase II Study to Evaluate Efficacy, Safety, and Pharmacokinetics of SC12267 (35 mg) in Combination With Methotrexate Compared to Methotrexate Alone in Patients With Rheumatoid Arthritis

Acronym: COMPONENT

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Nov 10, 2009
Registry last updated
Mar 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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