A Study of the Safety, Tolerability and Efficacy of Treatment With AP1189 in Early RA Patients With Active Joint Disease

NCT ID: NCT04004429

Last Updated: 2024-07-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 105 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-08-26
• Study Completion Date: 2021-11-16

Brief Summary

This is a multicenter, two-part, randomized, double-blind, placebo-kontrolled, 4-week study with repeated doses of AP1189. The study population will consist of newly diagnosed subjects with severe active Rheumatoid Arthritis, defined with a Clinical Disease Activity score (CDAI) > 22, who are to start up-titration with methotrexate.

Detailed Description

A multicenter, two-part, randomized, double-blind, placebo-kontrolled, 4-week study with repeated doses of AP1189. The study population will consist of newly diagnosed subjects with severe active Rheumatoid Arthritis, defined with a Clinical Disease Activity score (CDAI) > 22, who are to start up-titration with methotrexate.

The study will be conducted in two parts separated by an interim analysis.

Part 1: The subjects will be randomized in a 1:1:1 ratio into: .

• AP1189 dose 50 mg
• AP1189 dose 100 mg
• placebo

INTERIM ANALYSIS

Part 2: All subjects will be randomized into either design 1, 2 or 3 based on data from the interim analysis.

• Design 1: AP1189 dose 50 mg or placebo in a 2:1 ratio
• Design 2: AP1189 dose 100 mg or placebo in a 2:1 ratio
• Design 3: Continue with the same doses as in Part 1

The purpose of this study is to determine the safety and efficacy of 2 doses of AP1189 compared with placebo after 4 weeks of treatment.

Conditions

Rheumatoid Arthritis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

50 mg AP1189

50 mg AP1189. The treatment is a 4 week treatment. Each daily dose will be administered as a suspension, i e. the powder will be added 50 ml water.

Group Type: EXPERIMENTAL

50 mg AP1189

Intervention Type: DRUG

50 mg AP1189 powder in bottle

100 mg AP1189

100 mg AP1189. The treatment is a 4 week treatment. Each daily dose will be administered as a suspension, i e. the powder will be added 50 ml water.

Group Type: EXPERIMENTAL

AP1189

Intervention Type: DRUG

100 mg AP1189 powder in bottle

Placebo

Placebo. The treatment is a 4 week treatment. Each daily dose will be administered as a suspension i e. the powder will be added 50 ml water.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo powder in bottle

Interventions

50 mg AP1189

50 mg AP1189 powder in bottle

Intervention Type: DRUG

AP1189

100 mg AP1189 powder in bottle

Intervention Type: DRUG

Placebo

Placebo powder in bottle

Intervention Type: DRUG

Other Intervention Names

AP1189

Eligibility Criteria

Inclusion Criteria

• Written informed consent has been obtained prior to initiating any study specific procedures
• Male and female subjects, 18 to 85 years of age
• Confirmed diagnosis of RA (Rheumatoid Arthritis) according to the 2010 American College of Rheumatology (ACR)/EULAR RA classification criteria
• Polyarthritis with joint swelling and tenderness of a minimum of three joints out of 68 joints tested
• Candidate for Methotrexate treatment
• Is about to begin treatment with MTX (Methotrexate)
• Tested positive for anti-CCP (Anti-cyclic citrullinated peptide) or RF (Rheumatoid Factor)
• Severe active RA (Clinical Disease Activity Index (CDAI)) > 22) at screening and baseline
• Negative QFG-IT (QuantiFERON-in-Tube test)
• Subjects should be able to complete the PRO (Patient Reported Outcome) questionnaires
• Females of child-bearing potential may only participate if using reliable means of contraception or are post-menopausal. Surgically sterilized women at least 6 months prior to screening
• Females of childbearing potential must have a negative pregnancy test at screening and baseline

Exclusion Criteria

• Participation in any other study involving investigational drug(s) within 4 weeks prior to study entry
• Major surgery within 8 weeks prior to screening or planned surgery within 1 month following randomization
• Rheumatic autoimmune disease other than RA, including SLE (systemic Lupus Erythematosus), MCTD (Mixed Connective Tissue Disease), scleroderma, polymyositis, or significant systemic involvement secondary to RA. Sjögren syndrome with RA is allowable
• Functional class IV as defined by the ACR Criteria for Classification of Functional Status in RA or wheelchair/bedbound
• Prior history of or current inflammatory joint disease other than RA
• Subjects with fibromyalgia
• Initiation or change in dose for NSAIDs within 2 weeks prior to dosing with the IMP (Investigational Medicinal Product)
• Corticosteroids are prohibited within 2 weeks prior to screening (and during the entire treatment period and until the final visit
• 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 (determined by a derived glomerular filtration rate (GFR) using Cockcroft Gault Formula of ≤30 mL/min/1,73 m2 calculated by the local lab)
• 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
• Pregnant women or nursing mothers
• History of alcohol, drug, or chemical abuse within the 6 months prior to screening
• Neuropathies or other painful conditions that might interfere with pain evaluation
• Body weight of >150 kg

• Evidence of moderate and/or severe organ dysfunction
• Abnormal chest x-ray (as per the discretion of the investigator
• Evidence of positive hepatitis serology
• Evidence of peptic ulcer disease

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

SynAct Pharma Aps

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ellen-Margrethe Hauge, Professor

Role: PRINCIPAL_INVESTIGATOR

Aarhus University Hospital

Espen A Haavardsholm, Concultant, PhD

Role: PRINCIPAL_INVESTIGATOR

Diakonhjemmet Hospital

Locations

Aarhus Universitetshospital

Aarhus, , Denmark

Diakonhjemmet Sykehus

Oslo, , Norway

Countries

Denmark; Norway

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

SynAct-CS002

Identifier Type: -

Identifier Source: org_study_id