Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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Not provided
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Not provided
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Not provided
| Name | Class |
|---|---|
| Abbott Japan Co.,Ltd | INDUSTRY |
| Eisai Co., Ltd. | INDUSTRY |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of the study is to assess the long-term safety, tolerability, and efficacy of repeated administration of adalimumab in adult Japanese subjects with rheumatoid arthritis.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adalimumab 40 mg eow | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| adalimumab | Biological | 40 mg every other week (eow), subcutaneous (sc) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Responders With American College of Rheumatology (ACR) Criteria Improvement of at Least 20%, 50%, and 70% (ACR 20/50/70 Responders) | Number of subjects with American College of Rheumatology (ACR) criteria improvement consisting of 20%, 50%, and 70% (ACR20, ACR50, and ACR70, respectively) reduction in tender or swollen joint counts [TJC or SJC, respectively] and 20%, 50%, and 70% improvement, respectively, in 3 of the following 5 criteria: [1] physician's global assessment of disease activity [PGA], [2] subject's assessment of disease activity, [3] subject's assessment of pain, [4] subject's assessment of functional disability via a health assessment questionnaire [HAQ], and [5] C-reactive protein [CRP]) at each visit | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Measure | Description | Time Frame |
|---|---|---|
| Mean Change From Baseline in Tender Joint Count (TJC, Max = 68), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in tender joint count (TJC, max = 68), a component of the ACR criteria, by visit | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
Not provided
Inclusion Criteria:
Exclusion Criteria:
A subject who experienced any of the following during the prior adalimumab sc dosing study:
A subject who has been prescribed excluded medications during previous adalimumab study.
History of clinically significant drug or alcohol abuse, intravenous (iv) drug abuse, active infection with listeria or tuberculosis (TB), lymphoma, leukemia, or any malignancy with the exception of successfully treated non- metastatic basal cell carcinoma of the skin.
A subject who experienced chronic or active infection or any major episode of infection requiring hospitalization or treatment with intravenous (iv) antibiotics within 30 days of entry into study or chronic use of oral antibiotics within 14 days of entry into study.
Preexisting or recent onset of central nervous system (CNS) demyelinating disorders.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Shigeki Hashimoto, Ph.D. | Abbott | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Tokyo | Metropolis | Japan | ||||
Not provided
Japanese subjects with moderate to severe rheumatoid arthritis (RA) in relatively good physical health excluding RA symptoms and who completed a preceding continuous repeated administration study of adalimumab (DE035X/D2E7-J081-003) who wished to continue treatment until approval of adalimumab in Japan.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Adalimumab 40 mg Eow | Adalimumab 40 mg subcutaneously (sc) administered every other week (eow) until approval of adalimumab in Japan. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Adalimumab 40 mg Eow | Adalimumab 40 mg subcutaneously (sc) administered every other week (eow) until approval of adalimumab in Japan. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Responders With American College of Rheumatology (ACR) Criteria Improvement of at Least 20%, 50%, and 70% (ACR 20/50/70 Responders) | Number of subjects with American College of Rheumatology (ACR) criteria improvement consisting of 20%, 50%, and 70% (ACR20, ACR50, and ACR70, respectively) reduction in tender or swollen joint counts [TJC or SJC, respectively] and 20%, 50%, and 70% improvement, respectively, in 3 of the following 5 criteria: [1] physician's global assessment of disease activity [PGA], [2] subject's assessment of disease activity, [3] subject's assessment of pain, [4] subject's assessment of functional disability via a health assessment questionnaire [HAQ], and [5] C-reactive protein [CRP]) at each visit | Analysis was based on observed data. | Posted | Number | participants | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
Not provided
Not provided
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Adalimumab 40 mg Eow | Adalimumab 40 mg subcutaneously (sc) administered every other week (eow) until approval of adalimumab in Japan. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Lymphadenitis | Blood and lymphatic system disorders |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Diarrhoea | Gastrointestinal disorders |
Due to the small population, statistical tests were not performed.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Medical Information Specialist | Abbott | 800-633-9110 |
Not provided
| ID | Term |
|---|---|
| D001172 | Arthritis, Rheumatoid |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D000068879 | Adalimumab |
| ID | Term |
|---|---|
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Mean Change From Baseline in Swollen Joint Count (SJC, Max = 66), a Component of the ACR Criteria, by Visit | Mean change from baseline(last assessment in preceding study prior to adalimumab injection) in the SJC (max = 66) component of the ACR criteria | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Mean Change From Baseline in Physician's Global Assessment of Disease Activity (PGA) Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Assessment), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in PGA (a visual analog scale from 0 - 100 mm with 100 mm being the worst possible assessment), a component of the ACR criteria, by visit. | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Mean Change From Baseline in Subject's Global Assessment of Disease Activity Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Assessment), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in subject's global assessment of disease activity (a visual analog scale from 0 - 100 mm with 100 mm being the worst case), a component of the ACR criteria, by visit | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Mean Change From Baseline (Last Assessment in Preceding Study Prior to Adalimumab Injection) in Subject's Assessment of Pain Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Pain), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in subject's assessment of pain (using a visual analog scale from 0 - 100 mm with 100 mm being the worst possible pain), a component of the ACR criteria, by visit | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Mean Change From Baseline in Disability Index of the Health Assessment Questionnaire [HAQ], a Component the of ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in disability index of the health assessment questionnaire [HAQ; includes 20 questions assessing physical function in 8 domains. The questions are evaluated on a scale from 0 - 3 to measure the ability to perform certain activities (0 = without any difficulty, 1 = with some difficulty, 2 = with much difficulty, and 3 = unable to do so).], a component the of ACR criteria, by visit | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Mean Change From Baseline in C-reactive Protein [CRP; mg/dL], a Component of the ACR Criteria, by Visit. | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in C-reactive protein [CRP; mg/dL], a component of the ACR criteria, by visit. | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Area Under the Curve (AUC; From Start of the Study to Each Study Visit) of Subjects' Who Improved at Least 20% in ACR Response Criteria (ACR20 Response) | Sum of the duration (from start of study to each study visit) when a subject with American College of Rheumatology (ACR) criteria improved by 20% (ACR20) in tender or swollen joint counts [TJC or SJC, respectively] and 20% improvement in 3 of the following 5 criteria: [1] Physician's global assessment (PGA), [2] subject's assessment of disease activity, [3] subject's assessment of pain, [4] subject's assessment of functional disability via a health assessment questionnaire [HAQ], and [5] C-reactive protein (CRP) | Every 6 weeks up to Week 24 and every 12 weeks thereafter |
| Number of Subjects With Morning Stiffness at Each Visit | The number of subjects with morning stiffness (assessed as present or absent) at each visit among those who had morning stiffness at baseline (21). | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
| Fukuoka |
| Prefecture |
| Japan |
| Hiroshima | Prefecture | Japan |
| Ibaraki | Prefecture | Japan |
| Nagasaki | Prefecture | Japan |
| Osaka | Prefecture | Japan |
| Saitama | Prefecture | Japan |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
Adalimumab 40 mg subcutaneously (sc) administered every other week (eow) until approval of adalimumab in Japan. |
|
|
| Secondary | Mean Change From Baseline in Tender Joint Count (TJC, Max = 68), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in tender joint count (TJC, max = 68), a component of the ACR criteria, by visit | Posted | Mean | Standard Deviation | TJC | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline in Swollen Joint Count (SJC, Max = 66), a Component of the ACR Criteria, by Visit | Mean change from baseline(last assessment in preceding study prior to adalimumab injection) in the SJC (max = 66) component of the ACR criteria | Posted | Mean | Standard Deviation | SJC | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline in Physician's Global Assessment of Disease Activity (PGA) Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Assessment), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in PGA (a visual analog scale from 0 - 100 mm with 100 mm being the worst possible assessment), a component of the ACR criteria, by visit. | Posted | Mean | Standard Deviation | mm on scale | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline in Subject's Global Assessment of Disease Activity Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Assessment), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in subject's global assessment of disease activity (a visual analog scale from 0 - 100 mm with 100 mm being the worst case), a component of the ACR criteria, by visit | Posted | Mean | Standard Deviation | mm on scale | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline (Last Assessment in Preceding Study Prior to Adalimumab Injection) in Subject's Assessment of Pain Using a Visual Analog Scale (0 - 100 mm With 100 mm Being the Worst Possible Pain), a Component of the ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in subject's assessment of pain (using a visual analog scale from 0 - 100 mm with 100 mm being the worst possible pain), a component of the ACR criteria, by visit | Posted | Mean | Standard Deviation | mm on scale | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline in Disability Index of the Health Assessment Questionnaire [HAQ], a Component the of ACR Criteria, by Visit | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in disability index of the health assessment questionnaire [HAQ; includes 20 questions assessing physical function in 8 domains. The questions are evaluated on a scale from 0 - 3 to measure the ability to perform certain activities (0 = without any difficulty, 1 = with some difficulty, 2 = with much difficulty, and 3 = unable to do so).], a component the of ACR criteria, by visit | Posted | Mean | Standard Deviation | units on a scale | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Mean Change From Baseline in C-reactive Protein [CRP; mg/dL], a Component of the ACR Criteria, by Visit. | Mean change from baseline (last assessment in preceding study prior to adalimumab injection) in C-reactive protein [CRP; mg/dL], a component of the ACR criteria, by visit. | Posted | Mean | Standard Deviation | mg/dL | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| Secondary | Area Under the Curve (AUC; From Start of the Study to Each Study Visit) of Subjects' Who Improved at Least 20% in ACR Response Criteria (ACR20 Response) | Sum of the duration (from start of study to each study visit) when a subject with American College of Rheumatology (ACR) criteria improved by 20% (ACR20) in tender or swollen joint counts [TJC or SJC, respectively] and 20% improvement in 3 of the following 5 criteria: [1] Physician's global assessment (PGA), [2] subject's assessment of disease activity, [3] subject's assessment of pain, [4] subject's assessment of functional disability via a health assessment questionnaire [HAQ], and [5] C-reactive protein (CRP) | Posted | Mean | Standard Deviation | Weeks | Every 6 weeks up to Week 24 and every 12 weeks thereafter |
|
|
|
| Secondary | Number of Subjects With Morning Stiffness at Each Visit | The number of subjects with morning stiffness (assessed as present or absent) at each visit among those who had morning stiffness at baseline (21). | Subjects analyzed (as-observed) include only those who had morning stiffness at baseline. | Posted | Number | participants | Every 6 weeks up to Week 24 and every 12 weeks thereafter up to study completion or discontinuation (final value) |
|
|
|
| 10 |
| 25 |
| 25 |
| 25 |
| Brugada syndrome | Cardiac disorders |
|
| Pyrexia | General disorders |
|
| Pyelonephritis | Infections and infestations |
|
| Sepsis | Infections and infestations |
|
| Tendon rupture | Injury, poisoning and procedural complications |
|
| C-reactive protein increased | Investigations |
|
| Arthralgia | Musculoskeletal and connective tissue disorders |
|
| Rheumatoid arthritis | Musculoskeletal and connective tissue disorders |
|
| Metastases to lymph nodes | Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
|
| Non-Hodgkin's Lymphoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
|
| Ovarian neoplasm | Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
|
| Rectal cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
|
| Calculus ureteric | Renal and urinary disorders |
|
| Upper respiratory tract inflammation | Respiratory, thoracic and mediastinal disorders |
|
| Dental caries | Gastrointestinal disorders |
|
| Gastritis | Gastrointestinal disorders |
|
| Vomiting | Gastrointestinal disorders |
|
| Enterocolitis | Gastrointestinal disorders |
|
| Nausea | Gastrointestinal disorders |
|
| Periodontitis | Gastrointestinal disorders |
|
| Adverse drug reaction | General disorders |
|
| Chest pain | General disorders |
|
| Injection site reaction | General disorders |
|
| Hepatic function abnormal | Hepatobiliary disorders |
|
| Nasopharyngitis | Infections and infestations |
|
| Cystitis | Infections and infestations |
|
| Gastroenteritis | Infections and infestations |
|
| Bronchitis | Infections and infestations |
|
| Herpes zoster | Infections and infestations |
|
| Pharyngitis | Infections and infestations |
|
| Rhinitis | Infections and infestations |
|
| Sinusitis | Infections and infestations |
|
| Tinea blanca | Infections and infestations |
|
| Tinea pedis | Infections and infestations |
|
| Upper respiratory tract infection | Infections and infestations |
|
| Contusion | Injury, poisoning and procedural complications |
|
| Arthropod sting | Injury, poisoning and procedural complications |
|
| Animal bite | Injury, poisoning and procedural complications |
|
| Fall | Injury, poisoning and procedural complications |
|
| Wound | Injury, poisoning and procedural complications |
|
| Blood glucose increased | Investigations |
|
| DNA antibody positive | Investigations |
|
| Blood alkaline phosphatase increased | Investigations |
|
| Blood triglycerides increased | Investigations |
|
| Lymphocyte percentage decreased | Investigations |
|
| Hyperuricaemia | Metabolism and nutrition disorders |
|
| Back pain | Musculoskeletal and connective tissue disorders |
|
| Dizziness | Nervous system disorders |
|
| Insomnia | Psychiatric disorders |
|
| Rhinorrhoea | Respiratory, thoracic and mediastinal disorders |
|
| Cough | Respiratory, thoracic and mediastinal disorders |
|
| Upper respiratory tract inflammation | Respiratory, thoracic and mediastinal disorders |
|
| Nasal congestion | Respiratory, thoracic and mediastinal disorders |
|
| Pharyngolaryngeal discomfort | Respiratory, thoracic and mediastinal disorders |
|
| Pharyngolaryngeal pain | Respiratory, thoracic and mediastinal disorders |
|
| Productive cough | Respiratory, thoracic and mediastinal disorders |
|
| Pruritus | Skin and subcutaneous tissue disorders |
|
| Eczema | Skin and subcutaneous tissue disorders |
|
| Rash | Skin and subcutaneous tissue disorders |
|
| Erythema | Skin and subcutaneous tissue disorders |
|
| Haemorrhage subcutaneous | Skin and subcutaneous tissue disorders |
|
| Rash erythematous | Skin and subcutaneous tissue disorders |
|
| Urticaria | Skin and subcutaneous tissue disorders |
|
| Dermatitis contact | Skin and subcutaneous tissue disorders |
|
| Hyperkeratosis | Skin and subcutaneous tissue disorders |
|
| Hypertension | Vascular disorders |
|
Disclosure agreements vary; most restrictive agreement states Medical Institution shall not disclose materials/information disclosed by Abbott Japan in connection with the Clinical Research, or information obtained by conducting the Clinical Research, to third parties without Abbott Japan's prior written approval. When Medical Institution intends to publish information obtained by conducting the Clinical Research, Medical Institution shall obtain Abbott Japan's prior written approval.
| D003240 |
| Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
| D007162 |
| Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|
| Title | Measurements |
|---|---|
|
| Week 0 - Week 24 |
|
| Week 0 - Week 36 |
|
| Week 0 - Week 48 |
|
| Week 0 - Week 60 |
|
| Week 0 - Week 72 |
|
| Week 0 - Week 84 |
|
| Week 0 - Week 96 |
|
| Week 0 - Week 108 |
|
| Week 0 - Week 120 |
|
| Week 0 - Week 132 |
|
| Week 0 - Week 144 |
|
| Week 0 - Week 156 |
|
| Week 0 - Week 168 |
|
| Week 0 - Week 180 |
|
| Week 0 - Week 192 |
|
| Week 0 - Week 204 |
|
| Week 0 - Week 216 |
|
| Week 0 - Week 228 |
|
| Week 0 - Week 240 |
|
| Week 0 - Week 252 |
|
| Week 0 - Week 264 |
|
| Title | Measurements |
|---|
|
| Week 18 |
|
| Week 24 |
|
| Week 36 |
|
| Week 48 |
|
| Week 60 |
|
| Week 72 |
|
| Week 84 |
|
| Week 96 |
|
| Week 108 |
|
| Week 120 |
|
| Week 132 |
|
| Week 144 |
|
| Week 156 |
|
| Week 168 |
|
| Week 180 |
|
| Week 192 |
|
| Week 204 |
|
| Week 216 |
|
| Week 228 |
|
| Week 240 |
|
| Week 252 |
|
| Week 264 |
|
| Final Value |
|