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Completed

NCT Number: NCT05516979

A Safety & Efficacy Study of Treatment With AP1189 in Rheumatoid Arthritis Patients naïve to DMARD Treatment

The study is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of 12 weeks daily treatment with 100 mg AP1189 in RA patients who are to start up-titration with methotrexate (MTX).

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Timofei Mosneaga Republican Clinical Hospital

Chisinau, Moldova

Who can participate

Healthy volunteers accepted: No

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

Main Inclusion Criteria:

  • Confirmed diagnosis of RA according to the 2010 ACR/EULAR RA classification criteria and are ACR class I-III
  • ≥ 6 swollen joints (based on 66 joint counts) and ≥ 6 tender joints (based on 68 joint counts).
  • Candidate for MTX treatment
  • Is about to begin treatment with MTX
  • Must meet at least one of the following parameters at Screening:
  • positive result for anti-CCP or RF
  • Serum CRP ≥ 6 mg/L
  • Highly active RA (CDAI > 22) at screening and baseline
  • Negative QuantiFERON-in-Tube test (QFG-IT)
  • Females of child-bearing potential must use of highly effective birth control method

Main Exclusion Criteria:

  • Major surgery (including joint operation) within 8 weeks prior to screening or planned surgery within 1 month following randomization
  • Rheumatic autoimmune disease other than RA, including systemic lupus erythematosus (SLE), mixed connective tissue disease (MCTD), scleroderma, polymyositis, or significant systemic involvement secondary to RA. Sjögren's syndrome with RA is allowable
  • Prior history of or current inflammatory joint disease other than RA
  • Subjects with fibromyalgia
  • Use of hydroxychloroquine within 4 weeks prior the Screening Visit
  • Initiation of, or change in existing NSAID treatment within 2 weeks prior to the baseline visit
  • Corticosteroids except inhaled or nasal formulations for seasonal allergy or asthma are prohibited within 2 weeks prior to screening
  • Evidence of serious uncontrolled concomitant cardiovascular, nervous system, pulmonary, renal, hepatic, endocrine, or gastrointestinal disease
  • Have prior renal transplant, current renal dialysis, or severe renal insufficiency
  • Uncontrolled disease states, such as asthma, psoriasis, or inflammatory bowel disease where flares are commonly treated with oral or parenteral corticosteroids
  • Evidence of active malignant disease (except basal cell carcinoma of the skin that has been excised and cured)
  • Neuropathies or other painful conditions that might interfere with pain evaluation
  • Body weight of >150 kg
  • HBsAg positive and/or Anti-HBc with sign of current infection.

Treatment and study plan

100 mg AP1189

Drug

AP1189 tablets for oral use

Other names: AP1189 tablets for oral use

Placebo

Drug

Matching placebo for oral use

Primary outcomes

  1. Number of reported AEs

    Time frame: 12 weeks

    Evaluation of the safety and tolerability of AP1189 on the number and severity of reported Adverse Events, compared with placebo

  2. Change in ACR20

    Time frame: 12 weeks

    The change in American College of Rheumatology 20% (ACR20) compared to baseline

Secondary outcomes

  1. Change in ACR50

    Time frame: 12 weeks

    The change in American College of Rheumatology 50% (ACR50) compared to baseline

  2. Change in ACR70

    Time frame: 12 weeks

    The change in American College of Rheumatology 70% (ACR70) compared to baseline

  3. Change in (CDAI)

    Time frame: 12 weeks

    The change Clinical Disease Activity Index (CDAI) compared to baseline

  4. Change in DAS-28

    Time frame: 12 weeks

    The change in DAS-28, based on a CRP value, compare to baseline

Sponsors and collaborators

Lead sponsor

SynAct Pharma Aps

Industry

Collaborators

  • NBCD A/S

Registry information

Official study title

A Double-blind, Multi-center, Randomized, Placebo-controlled Study of the Safety and Efficacy of 12 Weeks Extended Treatment With AP1189 in Early Rheumatoid Arthritis (RA) Patients naïve to DMARD Treatment

Acronym: EXPAND

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Aug 26, 2022
Registry last updated
Nov 7, 2023

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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