MedPath

Long Term Open Label Continuation Study

Phase 3
Completed
Conditions
Rheumatoid Arthritis
Interventions
Biological: Adalimumab
Registration Number
NCT00195650
Lead Sponsor
Abbott
Brief Summary

The purpose of the study was to assess the long-term safety and clinical efficacy following repeated administration of adalimumab in patients with rheumatoid arthritis.

Detailed Description

Study DE020 was a multicenter, open-label continuation study for patients with rheumatoid arthritis who had participated in a prior Phase 1, 2, or 3 adalimumab study in the United States or Canada, had a favorable safety and efficacy profile when treated with adalimumab, and met the eligibility criteria for the continuation study. Participants received subcutaneous injections of adalimumab every other week (eow) or monthly based on the adalimumab regimen received in the prior study (i.e., participants who received monthly dosing in the prior study began the continuation study on monthly dosing; all other participants began adalimumab dosing at eow intervals). Participants who maintained an American College of Rheumatology 50% (ACR50) response for 2 consecutive visits could have their dosing interval lengthened to a monthly dosing schedule. Safety and efficacy data were collected over 520 weeks (10 years). Both safety and efficacy data were analyzed using all participants who received at least 1 dose of open-label adalimumab in the 10-year continuation study DE020 (the Full Analysis Set, n=846). Three patients who entered the continuation study but were never dosed were excluded from all analyses.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
846
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AdalimumabAdalimumabOpen-label adalimumab 40 mg
Primary Outcome Measures
NameTimeMethod
Number of Participants Meeting American College of Rheumatology 20% (ACR20) Response Criteria at Week 520Week 520

ACR20 response criteria were: \>=20% improvement in tender joint count; \>=20% improvement in swollen joint count; and \>=20% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants Meeting American College of Rheumatology 20% (ACR20) Response Criteria at Week 260Week 260

ACR20 response criteria were: \>=20% improvement in tender joint count; \>=20% improvement in swollen joint count; and \>=20% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants Meeting American College of Rheumatology 50% (ACR50) Response Criteria at Week 520Week 520

ACR50 response criteria were: \>=50% improvement in tender joint count; \>=50% improvement in swollen joint count; and \>=50% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants Meeting American College of Rheumatology 50% (ACR50) Response Criteria at Week 260Week 260

ACR50 response criteria were: \>=50% improvement in tender joint count; \>=50% improvement in swollen joint count; and \>=50% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants Meeting American College of Rheumatology 70% (ACR70) Response Criteria at Week 520Week 520

ACR70 response criteria were: \>=70% improvement in tender joint count; \>=70% improvement in swollen joint count; and \>=70% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants Meeting American College of Rheumatology 70% (ACR70) Response Criteria at Week 260Week 260

ACR70 response criteria were: \>=70% improvement in tender joint count; \>=70% improvement in swollen joint count; and \>=70% improvement in at least 3 of the 5 remaining ACR core measures: patient assessment of pain; patient global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response). All improvements were assessed relative to the baseline of the prior study.

Number of Participants in Clinical Remission (Based on Modified Disease Activity Score) at Week 520Week 520

Clinical remission on modified Disease Activity Score (DAS28) was a value \<2.6; \>=2.6 to \<=3.2 indicated low disease activity; \>3.2 to \<=5.1 indicated moderate disease activity; and \>5.1 indicated high disease activity. DAS28 score is calculated using the number of tender joints and swollen joints (out of 28 each), patient global assessment of disease activity, and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response).

Number of Participants in Clinical Remission (Based on Modified Disease Activity Score) at Week 260Week 260

Clinical remission on modified Disease Activity Score (DAS28) was a value \<2.6; \>=2.6 to \<=3.2 indicated low disease activity; \>3.2 to \<=5.1 indicated moderate disease activity; and \>5.1 indicated high disease activity. DAS28 score is calculated using the number of tender joints and swollen joints (out of 28 each), patient global assessment of disease activity, and C-reactive protein (a laboratory marker of inflammation that is sensitive to acute changes in inflammatory response).

Change From Baseline in the Disability Index of the Health Assessment Questionnaire (HAQ) at Week 520Baseline of prior Phase 1, 2, or 3 adalimumab study and Week 520

The HAQ-DI is a measure of disability that ranges from 0 to 3. Decrease in score indicates improvement in physical function; a decrease of 0.22 or greater from Baseline score is clinically significant. Participants assessed their ability to perform at least 6 of the following 8 specific tasks (1. dress/groom; 2. arise; 3. eat; 4. walk; 5. reach; 6. grip; 7. maintain hygiene; 8. maintain daily activity) over the past week by marking their response on a questionnaire. Possible responses/scores included the following: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). The 8 task scores are added and the sum is divided by the number of tasks assessed (range = 6 to 8). This yields a HAQ-DI score of 0 to 3.

Change From Baseline in the Disability Index of the Health Assessment Questionnaire (HAQ) at Week 260Baseline of prior Phase 1, 2, or 3 adalimumab study and Week 260

The HAQ-DI is a measure of disability that ranges from 0 to 3. Decrease in score indicates improvement in physical function; a decrease of 0.22 or greater from Baseline score is clinically significant. Participants assessed their ability to perform at least 6 of the following 8 specific tasks (1. dress/groom; 2. arise; 3. eat; 4. walk; 5. reach; 6. grip; 7. maintain hygiene; 8. maintain daily activity) over the past week by marking their response on a questionnaire. Possible responses/scores included the following: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). The 8 task scores are added and the sum is divided by the number of tasks assessed (range = 6 to 8). This yields a HAQ-DI score of 0 to 3.

Secondary Outcome Measures
NameTimeMethod
Reported Adverse EventsDuration of study (up to 520 weeks [10 years])

Adverse events were collected during the course of the study (after the first adalimumab injection in this continuation study DE020 through 70 days after the last adalimumab injection) for all participants who received at least 1 dose of open-label adalimumab in the continuation study (Full Analysis Set). The number of participants experiencing any adverse event (serious and non-serious) are summarized. See the Reported Adverse Events section for details.

Trial Locations

Locations (92)

Site Reference ID/Investigator# 541

🇺🇸

Danbury, Connecticut, United States

Site Reference ID/Investigator# 574

🇺🇸

Fort Myers, Florida, United States

Site Reference ID/Investigator# 646

🇺🇸

Statesville, North Carolina, United States

Site Reference ID/Investigator# 653

🇺🇸

Boston, Massachusetts, United States

Site Reference ID/Investigator# 408

🇺🇸

Anchorage, Alaska, United States

Site Reference ID/Investigator# 4113

🇺🇸

Mobile, Alabama, United States

Site Reference ID/Investigator# 555

🇺🇸

Los Angeles, California, United States

Site Reference ID/Investigator# 579

🇺🇸

Orlando, Florida, United States

Site Reference ID/Investigator# 571

🇺🇸

Palm Harbor, Florida, United States

Site Reference ID/Investigator# 651

🇺🇸

Sarasota, Florida, United States

Site Reference ID/Investigator# 537

🇺🇸

Tucson, Arizona, United States

Site Reference ID/Investigator# 431

🇺🇸

Fort Lauderdale, Florida, United States

Site Reference ID/Investigator# 650

🇺🇸

Coeur D'Alene, Idaho, United States

Site Reference ID/Investigator# 3412

🇺🇸

Upland, California, United States

Site Reference ID/Investigator# 387

🇺🇸

Los Angeles, California, United States

Site Reference ID/Investigator# 544

🇺🇸

Chevy Chase, Maryland, United States

Site Reference ID/Investigator# 66864

🇺🇸

Santa Monica, California, United States

Site Reference ID/Investigator# 3440

🇨🇦

Montreal, Canada

Site Reference ID/Investigator# 557

🇺🇸

La Jolla, California, United States

Site Reference ID/Investigator# 535

🇺🇸

Stanford, California, United States

Site Reference ID/Investigator# 655

🇺🇸

Wilmington, Delaware, United States

Site Reference ID/Investigator# 455

🇺🇸

Daytona Beach, Florida, United States

Site Reference ID/Investigator# 576

🇺🇸

Vancouver, Washington, United States

Site Reference ID/Investigator# 4110

🇺🇸

Boise, Idaho, United States

Site Reference ID/Investigator# 4112

🇺🇸

Indianapolis, Indiana, United States

Site Reference ID/Investigator# 413

🇨🇦

Montreal, Canada

Site Reference ID/Investigator# 534

🇺🇸

Metairie, Louisiana, United States

Site Reference ID/Investigator# 449

🇺🇸

Boise, Idaho, United States

Site Reference ID/Investigator# 66807

🇨🇦

North York, Canada

Site Reference ID/Investigator# 649

🇺🇸

Everett, Washington, United States

Site Reference ID/Investigator# 412

🇺🇸

Olympia, Washington, United States

Site Reference ID/Investigator# 565

🇨🇦

Hamilton, Canada

Site Reference ID/Investigator# 2466

🇨🇦

Toronto, Canada

Site Reference ID/Investigator# 567

🇨🇦

Toronto, Canada

Site Reference ID/Investigator# 3442

🇨🇦

Vancouver, Canada

Site Reference ID/Investigator# 438

🇺🇸

Cincinnati, Ohio, United States

Site Reference ID/Investigator# 2467

🇨🇦

Sainte-Foy, Quebec, Canada

Site Reference ID/Investigator# 414

🇨🇦

Ottawa, Canada

Site Reference ID/Investigator# 66804

🇨🇦

Scarborough, Canada

Site Reference ID/Investigator# 563

🇨🇦

St. John's, Canada

Site Reference ID/Investigator# 514

🇨🇦

Winnipeg, Canada

Site Reference ID/Investigator# 538

🇺🇸

Birmingham, Alabama, United States

Site Reference ID/Investigator# 4111

🇺🇸

Birmingham, Alabama, United States

Site Reference ID/Investigator# 4109

🇺🇸

Denver, Colorado, United States

Site Reference ID/Investigator# 532

🇺🇸

Portland, Oregon, United States

Site Reference ID/Investigator# 539

🇺🇸

Milwaukee, Wisconsin, United States

Site Reference ID/Investigator# 542

🇺🇸

Tampa, Florida, United States

Site Reference ID/Investigator# 652

🇺🇸

Zephyrhills, Florida, United States

Site Reference ID/Investigator# 415

🇺🇸

Vero Beach, Florida, United States

Site Reference ID/Investigator# 66862

🇺🇸

Everett, Washington, United States

Site Reference ID/Investigator# 654

🇺🇸

Milford, Connecticut, United States

Site Reference ID/Investigator# 66863

🇺🇸

St. Petersburg, Florida, United States

Site Reference ID/Investigator# 578

🇺🇸

Chicago, Illinois, United States

Site Reference ID/Investigator# 658

🇺🇸

Spokane, Washington, United States

Site Reference ID/Investigator# 547

🇺🇸

Louisville, Kentucky, United States

Site Reference ID/Investigator# 551

🇺🇸

Yakima, Washington, United States

Site Reference ID/Investigator# 531

🇺🇸

Kirkland, Washington, United States

Site Reference ID/Investigator# 513

🇨🇦

Calgary, Canada

Site Reference ID/Investigator# 656

🇺🇸

Glendale, Wisconsin, United States

Site Reference ID/Investigator# 568

🇨🇦

Charlottetown, Canada

Site Reference ID/Investigator# 566

🇨🇦

Pointe-Claire, Canada

Site Reference ID/Investigator# 564

🇨🇦

Hamilton, Canada

Site Reference ID/Investigator# 569

🇨🇦

Kitchener, Canada

Site Reference ID/Investigator# 66805

🇨🇦

North York, Canada

Site Reference ID/Investigator# 66822

🇺🇸

Anaheim, California, United States

Site Reference ID/Investigator# 572

🇺🇸

Colorado Springs, Colorado, United States

Site Reference ID/Investigator# 552

🇺🇸

Santa Barbara, California, United States

Site Reference ID/Investigator# 451

🇺🇸

Westlake Village, California, United States

Site Reference ID/Investigator# 66843

🇺🇸

Gainesville, Florida, United States

Site Reference ID/Investigator# 577

🇺🇸

St. Louis, Missouri, United States

Site Reference ID/Investigator# 546

🇺🇸

Petoskey, Michigan, United States

Site Reference ID/Investigator# 66842

🇺🇸

Toms River, New Jersey, United States

Site Reference ID/Investigator# 4114

🇺🇸

Worcester, Massachusetts, United States

Site Reference ID/Investigator# 573

🇺🇸

Dover, New Jersey, United States

Site Reference ID/Investigator# 561

🇺🇸

Reno, Nevada, United States

Site Reference ID/Investigator# 549

🇺🇸

Billings, Montana, United States

Site Reference ID/Investigator# 559

🇺🇸

Voorhees, New Jersey, United States

Site Reference ID/Investigator# 432

🇺🇸

Lake Success, New York, United States

Site Reference ID/Investigator# 562

🇺🇸

Albuquerque, New Mexico, United States

Site Reference ID/Investigator# 545

🇺🇸

Port Jefferson Station, New York, United States

Site Reference ID/Investigator# 647

🇺🇸

New York, New York, United States

Site Reference ID/Investigator# 66823

🇺🇸

Brooklyn, New York, United States

Site Reference ID/Investigator# 657

🇺🇸

New York, New York, United States

Site Reference ID/Investigator# 540

🇺🇸

Syracuse, New York, United States

Site Reference ID/Investigator# 436

🇺🇸

Dayton, Ohio, United States

Site Reference ID/Investigator# 548

🇺🇸

Bend, Oregon, United States

Site Reference ID/Investigator# 553

🇺🇸

Eugene, Oregon, United States

Site Reference ID/Investigator# 570

🇺🇸

Bethlehem, Pennsylvania, United States

Site Reference ID/Investigator# 575

🇺🇸

Ridley Park, Pennsylvania, United States

Site Reference ID/Investigator# 2435

🇺🇸

Dallas, Texas, United States

Site Reference ID/Investigator# 585

🇺🇸

Willow Grove, Pennsylvania, United States

Site Reference ID/Investigator# 536

🇺🇸

Richmond, Virginia, United States

© Copyright 2025. All Rights Reserved by MedPath