A Study to Assess Safety and Efficacy of ASP015K in Participants With Rheumatoid Arthritis (RA) Who Had an Inadequate Response or Intolerance to Methotrexate (MTX)

Rheumatoid Arthritis (RA) Clinical Trial

Official title:

A Randomized, Double-Blind, Placebo-Controlled Confirmatory Study of the Safety and Efficacy of ASP015K in Patients With Rheumatoid Arthritis (RA) Who Had an Inadequate Response or Intolerance to MTX

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03660059
• Other study ID #: 015K-CL-CNA3
• Secondary ID: CTR20181199
• Status: Completed
• Phase: Phase 3
• Start date: September 27, 2018
• Est. completion date: November 2, 2021

Study information

• Verified date: April 2024
• Source: Astellas Pharma Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to verify the superiority of ASP015K in combination with MTX or with other disease-modifying antirheumatic drugs (DMARDs) over placebo in terms of efficacy in participants with rheumatoid arthritis (RA) who had an inadequate response or intolerance to MTX, as measured by the American College of Rheumatology (ACR) 20 response rate at Week 24.

This study will also evaluate the pharmacokinetics and safety of ASP015K as well as efficacy and safety of long-term treatment with ASP015K (52 weeks).

Description:

Participants will be randomized in a 1:1:1 ratio to the ASP015K dose-A group, ASP015K dose-B group or placebo group at Week 0.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 385
• Est. completion date: November 2, 2021
• Est. primary completion date: April 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subject is a man or woman and considered to be an adult, according to the local legal definition, at the time of informed consent.

• Subject has RA diagnosed according to the 1987 American College of Rheumatology (ACR) criteria or the 2010 American College of Rheumatology/European League against Rheumatism (ACR/EULAR) criteria.

• Subject did not receive the following drugs, or received the drugs with stable dosage for at least 28 days prior to the baseline (start of treatment) for RA treatment: Non-steroidal anti-inflammatory drugs (NSAIDs; excluding topical formulations), oral morphine or equivalent opioid analgesics (= 30 mg/day), acetaminophen, or oral corticosteroids (= 10 mg/day in prednisolone equivalent).

• Subject has active RA as evidenced by both of the following:

• = 6 tender/painful joints (using 68-joint assessment)

• = 6 swollen joints (using 66-joint assessment)

• Subject has CRP > 0.50 mg/dL. The re-test of CRP will be allowed, if the subject's CRP value at the time of screening test is more than 0.30 mg/dL and also his/her most recent CRP value which was carried out up to 90 days before the date of screening test was more than 0.5 mg/dL.

• Subject meets the ACR 1991 Revised Criteria for the Classification of Global Functional Status in RA Class I, II, or III.

• Subject has inadequate response or intolerance for MTX.

• For inadequate responder to MTX, subject has had regular use of MTX for at least 90 days prior to screening at a dose that, in accordance with local clinical practice, is considered acceptable to adequately assess clinical response. The dose of MTX must have been a stable, unchanging oral dose of 7.5 to 20 mg/week (or the equivalent injectable dose) for at least the 28 days prior to screening. Subject is able to continue stable dose of MTX from at least 28 days prior to screening until the end of the administration period of study drug.

• For subject who is intolerant of MTX, subject has had regular use of the following DMARDs, and when the following DMARDs are concomitantly administered to subject, the drugs must be administered for at least 90 days prior to screening, and must be stable from at least 28 days prior to screening until the end of the administration period of study drug.

• Hydroxychloroquine

• Salazosulfapyridine

• Gold

• D-penicillamine

• Lobenzarit

• Actarit

• Bucillamine

• Iguratimod

Exclusion Criteria:

• Subject has received a biologic DMARD within the specified period:

• Anakinra: within 28 days prior to baseline

• Etanercept: within 28 days prior to baseline

• Adalimumab, infliximab: within 56 days prior to baseline

• Golimumab, certolizumab pegol: within 70 days prior to baseline

• Abatacept, tocilizumab: within 84 days prior to baseline

• Denosumab: within 150 days prior to baseline

• Rituximab: within 180 days prior to baseline

• Subject has inadequate response to at least 3 biologic DMARDs.

• Subject has received a non-biologic DMARD listed below or other drugs used in the treatment of RA within 28 days prior to baseline. Leflunomide is prohibited within 90 days prior to baseline. Alternatively, leflunomide is prohibited at least 28 days prior to baseline if washout with cholestyramine for at least 17 days is completed within 28 days prior to baseline. However, topical drugs other than those for the treatment of RA may be used concomitantly.

• Leflunomide

• Tacrolimus

• Cyclosporine

• Cyclophosphamide

• Azathioprine

• Minocycline

• Mizoribine

• Subject has received Chinese herbal medicines listed below or other herbal drugs used in the treatment of RA within 28 days prior to baseline.

• Tripterygium wilfordii

• Total glucosides of paeony

• Tsuduranine

• Subject has received tofacitinib, baricitinib or other JAK inhibitor (including other investigational drugs).

• Subject has received intra-articular, intravenous, intramuscular, or endorectal (including suppositories for anal diseases) corticosteroid within 28 days prior to baseline.

• Subject has participated in any study of ASP015K and has received ASP015K or placebo.

• Subject has received other investigational drugs within 90 days or within 5 half-lives, whichever is longer, prior to baseline.

• Subject has received plasma exchange therapy within 60 days prior to baseline.

• Subject has undergone joint drainage, has received local anesthesia and nerve block, or has received articular cartilage protectant (such as glucosamine sulfate, chondroitin sulfate these DMORD medicine) at the assessed joint within 28 days prior to baseline.

• Subject has undergone surgery and has residual effects in the assessed joints or is scheduled to undergo surgery that may affect the study evaluation of the assessed joints.

• Subject is diagnosed as inflammatory arthritis (psoriatic arthritis, ankylosing spondylitis, SLE, sarcoidosis, etc.) other than RA.

• Subject has any of the following laboratory values:

• Hemoglobin < 9.0 g/dL

• Absolute neutrophil count < 1000/µL

• Absolute lymphocyte count < 800/µL

• Platelet count < 75000/µL

• Alanine aminotransferase (ALT) = 2 × upper limit of normal (ULN)

• Aspartate aminotransferase (AST) = 2 × ULN

• Total bilirubin (TBL) = 1.5 × ULN

• Estimated glomerular filtration rate (eGFR) = 40 mL/min as measured by the MDRD method

• ß-D-glucan > ULN

• Subject has a history of or concurrent active tuberculosis (TB). Eligibility criteria for TB are tabulated below:

• Subject meets any of the following in terms of infection except for TB:

• History of or concurrent severe herpes zoster (associated with Hunt syndrome or having ulcerative lesions) or disseminated herpes zoster

• History of multiple recurrences (at least twice) of localized herpes zoster

• Serious infection requiring hospitalization within 90 days prior to baseline

• Subject has received intravenous antibiotics within 90 days prior to baseline. (However, prophylactic antibiotics are allowed.)

• Subject with high risk of infection (e.g., subject with urinary catheter)

• Subject has a history of or concurrent interstitial pneumonia and inappropriate to participate in this study.

• Subject has a history of or concurrent malignant tumor (except for successfully treated basal cell carcinoma).

• Subject has received live or live attenuated virus vaccination within 56 days prior to baseline. (Inactivated vaccines including influenza and pneumococcal vaccines are allowed.)

• Subject has any ongoing severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, metabolic, endocrine, pulmonary, cardiac, neurological, infectious, or autoimmune disease except for RA (excluding Sjogren's syndrome and chronic thyroiditis), or any ongoing illness which would make the subject unsuitable for the study.

• Subject has a history of clinically significant allergy. (Clinically significant allergy includes allergies such as systemic urticaria induced by specific antigens and drugs, anaphylaxis, and allergy associated with shock necessitating hospitalized treatment.)

• Subject has received medications that are CYP3A substrates with narrow therapeutic range within 14 days prior to baseline. These medications include: dihydroergotamine, ergotamine, fentanyl, pimozide, quinidine, temsirolimus, and disopyramide.

• Subject has concurrent cardiac failure, defined as New York Heart Association (NYHA) classification Class III or higher, or a history of it.

• Subject has concurrent prolonged QT syndrome or a history of it. Subject has prolonged QT interval (defined as QTc = 500 msec. Subject has QTc = 500 msec at retest will be excluded).

• Subject has congenital short QT syndrome or a history of it. Subject has shortened QT interval (defined as QTc < 330 msec. Subject has QTc < 330 msec at retest will be excluded).

• Subject has a history of positive HIV infection.

• Female subject is pregnant or might be pregnant, is nursing, wishes to conceive for a period running from the time informed consent is given within 60 days after end of treatment, or for whom the possibility of pregnancy cannot be ruled out as a result of the serum pregnancy test given at the time of screening.

• Male subject cannot practice at least 2 types of contraception from the time of informed consent to 90 days after end of treatment, or subject is a woman with childbearing potential who cannot practice at least 2 types of contraception from the time of informed consent to 60 days after end of treatment.

• Male subject does not agree not to donate sperm starting at informed consent and through the treatment period and for at least 90 days after final study drug administration. Female subject who do not agree not to donate ova starting at informed consent through the treatment period and for 60 days after final study drug administration.

• Subject has a history or complication of lymphatic diseases such as lymphoproliferative disorder, lymphoma, and leukemia.

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Rheumatoid Arthritis (RA)

Intervention

Drug:
• Peficitinib
Oral
• Plaebo
Oral
• Disease-modifying antirheumatic drugs (DMARDs)
As necessary concomitant medications, DMARDs listed below will be administered orally unless specified. For subjects who are inadequate responders to methotrexate (MTX): MTX. For subjects who are intolerant of MTX: either of DMARDs listed; hydroxychloroquine, salazosulfapyridine, gold (injection or oral), D-penicillamine, lobenzarit, actarit, bucillamine and iguratimod.

Locations

Country	Name	City	State
China	Site CN00048	Anhui
China	Site CN00045	Beijing
China	Site CN00054	Beijing
China	Site CN00050	Bengbu
China	Site CN00061	Changchun
China	Site CN00032	Changsha
China	Site CN00076	Chenzhou
China	Site CN00071	Guangdong
China	Site CN00016	Guangzhou
China	Site CN00052	Guangzhou
China	Site CN00063	Guangzhou
China	Site CN00072	Guangzhou
China	Site CN00058	Inner Mongolia
China	Site CN00074	Jieyang
China	Site CN00028	Jilin
China	Site CN00069	Jining
China	Site CN00064	Jiujiang
China	Site CN00046	Kunming
China	Site CN00060	Nanjing
China	Site CN00070	Nanjing
China	Site CN00068	Ningbo
China	Site CN00075	Pingxiang
China	Site CN00066	Qingdao
China	Site CN00056	Shanghai
China	Site CN00047	Shantou
China	Site CN00053	Sichuan
China	Site CN00057	Tianjin
China	Site CN00062	Tianjin
China	Site CN00059	Wuhan
China	Site CN00067	Xining
China	Site CN00065	Xuzhou
China	Site CN00073	Zhengzhou
China	Site CN00049	Zhuzhou
Korea, Republic of	Site KR00037	Gwangju
Korea, Republic of	Site KR00036	Incheon
Korea, Republic of	Site KR00033	Seoul
Korea, Republic of	Site KR00034	Seoul
Korea, Republic of	Site KR00035	Seoul
Taiwan	Site TW00022	Taichung
Taiwan	Site TW00023	Taichung
Taiwan	Site TW00024	Taichung
Taiwan	Site TW00025	Taipei
Taiwan	Site TW00026	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
Astellas Pharma China, Inc.

Countries where clinical trial is conducted

China,  Korea, Republic of,  Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	American College of Rheumatology (ACR)20 response rate at Week 24	The ACR20 response requires that all criteria from (1) to (3) be met compared with Week 0 (baseline); (1), Tender Joint Count (TJC) >= 20% reduction; (2), Swollen Joint Count (SJC) >= 20% reduction;(3) >= 20% improvement in three or more of the following five parameters - [1] subject's assessment of pain, [2] Subject's Global Assessment of Arthritis (SGA), [3] Physician's Global Assessment of Arthritis (PGA), [4] health assessment questionnaire-disability index (HAQ-DI), [5] acute phase reactant (C-reactive protein (CRP) or erythrocyte sedimentation rate (ESR)).	At Week 24
Secondary	ACR20 response rate	The ACR20 response requires that all criteria from (1) to (3) be met compared with Week 0 (baseline); (1), Tender Joint Count (TJC) >= 20% reduction; (2), Swollen Joint Count (SJC) >= 20% reduction;(3) >= 20% improvement in three or more of the following five parameters - [1] subject's assessment of pain, [2] Subject's Global Assessment of Arthritis (SGA), [3] Physician's Global Assessment of Arthritis (PGA), [4] health assessment questionnaire-disability index (HAQ-DI), [5] acute phase reactant (C-reactive protein (CRP) or erythrocyte sedimentation rate (ESR)).	Up to Week 52
Secondary	ACR50 response rate	The ACR50 response indicates a 50% improvement in all criteria used in the ACR20 assessment.	Up to Week 52
Secondary	ACR70 response rate	The ACR70 response indicates a 70% improvement in all criteria used in the ACR70 assessment.	Up to Week 52
Secondary	Change from baseline in disease activity score (DAS) 28-C-reactive protein (CRP) scores	DAS28-CRP will be calculated using data from TJC (28 joints), SJC (28 joints), CRP and SGA with the formula; DAS28-CRP = 0.56v(TJC) + 0.28v(SJC) + 0.36 ln (CRP + 1) + 0.014 x SGA + 0.96	From baseline (Week 0) to Week 52
Secondary	Change from baseline in DAS28- erythrocyte sedimentation rate (ESR) scores	DAS28-ESR will be calculated using data from TJC (28 joints), SJC (28 joints), ESR and SGA with the formula; DAS28- ESR = 0.56v(TJC) + 0.28v(SJC) + 0.70 ln ESR + 0.014 x SGA	From baseline (Week 0) to Week 52
Secondary	Change from baseline in Tender Joint Count (TJC) (68 joints)	The investigator/sub-investigator will examine the participant for tender joints, assessing the 68 joints and confirm the location of each tender joint.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in Swollen Joint Count (SJC) (66 joints)	The investigator/sub-investigator will examine the participants for swollen joints, assessing the 66 joints, where hip joints are excluded from 68 joints, and confirm the location of the swollen joints.	From baseline (Week 0) to Week 52
Secondary	Percentage of participants achieving DAS28-CRP scores for remission	Percentage of participants with DAS28 scores less than 2.6.	Up to Week 52
Secondary	Percentage of participants achieving DAS28-ESR scores for remission	Percentage of participants with DAS28 scores less than 2.6.	Up to Week 52
Secondary	Percentage of participants achieving low disease activity by DAS28-CRP	DAS28 score exceeding 5.1 is considered high disease activity; 3.2 to 5.1, moderate disease activity; less than 3.2, low disease activity.	Up to Week 52
Secondary	Percentage of participants achieving low disease activity by DAS28-ESR	DAS28 score exceeding 5.1 is considered high disease activity; 3.2 to 5.1, moderate disease activity; less than 3.2, low disease activity.	Up to Week 52
Secondary	Change from baseline in CRP	CRP will be measured with blood samples.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in ESR	ESR will be measured with blood samples.	From baseline (Week 0) to Week 52
Secondary	Percentage of participants with good European League Against Rheumatism (EULAR) response	Based on DAS28 scores and changes in DAS28 scores before and after treatment with the study drug, EULAR Response Criteria categorize response to treatment as "No response", "Moderate response," or "Good response."	Up to Week 52
Secondary	Percentage of participants with good or moderate EULAR response	Based on DAS28 scores and changes in DAS28 scores before and after treatment with the study drug, EULAR Response Criteria categorize response to treatment as "No response", "Moderate response," or "Good response."	At Week 52
Secondary	Percentage of participants achieving ACR/EULAR remission	If all of the following 4 parameters are fulfilled, it is defined as remission: TJC = 1, SJC = 1, CRP = 1 mg/dL, SGA = 1 cm (on a visual analog scale (VAS) of 0 - 100 mm).	At Week 52
Secondary	Percentage of participants achieving Simplified Disease Activity Index (SDAI) remission (SDAI score = 3.3)	SDAI score will be calculated with formula SDAI = TJC + SJC + SGA + PGA + CRP. SDAI score exceeding 26 is considered high disease activity; exceeding 11 and not greater than 26, moderate disease activity; exceeding 3.3 and not greater than 11, low disease activity.	Up to Week 52
Secondary	Change from baseline in SDAI score	Change from baseline (Week 0) in SDAI score will be calculated.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in Physician's Global Assessment of Arthritis (PGA) (VAS)	The investigator/sub-investigator assesses the participant's disease activity on a VAS of 0 - 100 mm on the physician assessment table.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in SGA (VAS)	The participant assesses his/her own disease activity on a VAS of 0 - 100 mm on the questionnaire form.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in participant's assessment of pain (VAS)	The participant assesses his/her own pain severity on a VAS of 0 - 100 mm on the questionnaire form.	From baseline (Week 0) to Week 52
Secondary	Incidence of participant withdrawal due to the lack of efficacy	Number of participants who withdraw from this study due to the lack of efficacy.	Up to Week 56
Secondary	Change from baseline in health assessment questionnaire-disability index (HAQ-DI) score	The HAQ-DI measure shave eight dimensions of functional activity: pruning, dressing, rising, eating, walking, personal hygiene, reach, grip, and other routine activities. Each item has 4 degrees ranging from 0 to 3. "0" refers to "no functional difficulty", "1" to a bit of functional difficulty, "2" to very much functional difficulty, and "3" to no ability to work. HAQ-DI score 0-1 means mild to moderate functional difficulty; 1-2 means moderate to severe disability; and 2-3 means generally severe disability.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in Short Form Health Survey - 36 questions, version 2 (SF-36v2)® score	SF-36v2 is a validated instrument used to measure general physical and mental health status via assessment of 8 domains - physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental. The SF-36 is scored using norm-based scoring procedures and scores ranging from 0-100; higher scores represent better health-related quality of life.	From baseline (Week 0) to Week 52
Secondary	Change from baseline in Work Productivity and Activity Impairment Questionnaire (WPAI) score	WPAI produces four types of scores: absenteeism (work time missed), presenteeism (impairment at work/reduced on-the-job effectiveness), work productivity loss (overall work impairment/absenteeism plus presenteeism), and activity impairment. The WPAI outcomes are expressed as impairment percentages, with higher numbers indicating greater impairment and less productivity, that is, worse outcomes.	From baseline (Week 0) to Week 52
Secondary	Pharmacokinetics (PK) of ASP015K in plasma: post-dose concentration	Post-dose concentration will be derived from the PK plasma samples collected.	2 hours post-dose at either Week 4 or Week 8
Secondary	PK of ASP015K in plasma: trough concentration (Ctrough)	Ctrough will be derived from the PK plasma samples collected.	Up to Week 52
Secondary	Safety assessed by incidence of adverse events (AEs)	An AE is defined as any untoward medical occurrence after the signing of informed consent form in a participant administered a study drug or who has undergone study procedures and which does not necessarily have a causal relationship with this treatment.	Up to Week 56
Secondary	Number of participants with vital sign abnormalities and/or AEs	Number of participants with potentially clinically significant vital sign values.	Up to Week 56
Secondary	Number of participants with body weight abnormalities and/or AEs	Number of participants with potentially clinically significant body weight values.	Up to Week 56
Secondary	Number of participants with 12-lead electrocardiogram (ECG) abnormalities and/or AEs	Number of participants with potentially clinically significant 12-ECG values.	Up to Week 52
Secondary	Number of participants with central ECG abnormalities and/or AEs	Number of participants with potentially clinically significant central ECG observations. Central ECG will be measured before and 2 hours after study drug administration.	Up to Week 8
Secondary	Number of participants with chest radiography abnormalities and/or AEs	Number of participants with potentially clinically significant chest radiography observations.	Up to Week 52

External Links

•   Link to plain language summary of the study on the Trial Results Summaries website
•   Link to results on the Astellas Clinical Study Results website