- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT01160822
To Determine the Safety, Tolerability, Pharmacokinetics and Effect on Pain of a Single Intra-articular Administration of Canakinumab in Patients With Osteoarthritis in the Knee
A Randomized, Double Blind, Placebo and Naproxen Controlled, Multi-center, Study to Determine the Safety, Tolerability, Pharmacokinetics and Effect on Pain of a Single Intra-articular Administration of Canakinumab in Patients With Osteoarthritis in the Knee
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
This is a randomized, double-blind, parallel group, placebo controlled 18 weeks study, consisting of two parts:
- Part A: an ascending single dose part in which the safety and tolerability of up to 4 different canakinumab doses are studied (starting dose 150 mg, maximum dose 600 mg).
- Part B: a double-dummy, active-controlled, parallel design part in which the pain reduction of the canakinumab dose selected from part A is studied in comparison to Placebo and Naproxen.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 2
Kontakty i lokalizacje
Lokalizacje studiów
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Helsinki, Finlandia
- Novartis Investigative Site
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Kuopio, Finlandia
- Novartis Investigative Site
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Creteil, Francja
- Novartis Investigative Site
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Berlin, Niemcy
- Novartis Investigative Site
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Erlangen, Niemcy
- Novartis Investigative Site
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Alabama
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Anniston, Alabama, Stany Zjednoczone, 36207
- Pinnacle Research Group, LLC
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Arizona
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Mesa, Arizona, Stany Zjednoczone, 85202
- Arizona Arthritis & Rheumatology Research, PLLC
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California
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San Diego, California, Stany Zjednoczone, 92108
- San Diego Arthritis & Osteoporosis Medical Clinic
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Westlake Village, California, Stany Zjednoczone, 91361
- Westlake Medical Research
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Illinois
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Chicago, Illinois, Stany Zjednoczone, 60612
- Rush-Presbyterian St. Lukes Medical Center
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Kansas
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Topeka, Kansas, Stany Zjednoczone, 66606
- Cotton O'Neil Clinical Research Institute
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Pennsylvania
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Duncansville, Pennsylvania, Stany Zjednoczone, 16635
- Altoona Center for Clinical Research
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Tennessee
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Knoxville, Tennessee, Stany Zjednoczone, 37920
- Volunteer Research Group
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Written informed consent must be obtained before any assessment is performed.
- Male and female patients aged 40 - 80 years (inclusive).
- Diagnosis of knee osteoarthritis
- Radiographic evidence of tibiofemoral compartment osteoarthritis
- Pain in the knee during the last 24 hours.The patients should also have had pain in the affected knee on most days over the last month.
- Patients who are willing to discontinue all non-steroidal anti-inflammatory drugs (NSAIDs) or other analgesic medication taken for any condition, including their knee pain,
- Patients who are on stable dose of opioids for at least 1 month before screening can continue to take their opioid at this stable dose throughout the study.
- Patients must also be willing to abstain from any intra-articular or peri-articular injections to the knee or surgery during the treatment period
- Patients who, if they are currently taking aspirin (325 mg/day or less; as anti-coagulants), are willing to remain on a stable dose one month prior to screening and throughout the study
Exclusion Criteria:
- Subjects with known hypersensitivity to any biological or investigational drugs.
- Patients with contraindications to knee injections
- Patients with joint effusion
- Patients should not have rheumatoid arthritis or any connective tissue like disease
- Secondary osteoarthritis with history and/or any evidence of the following diseases: septic arthritis, inflammatory joint disease, gout, Paget's disease of the bone, articular fracture, major dysplasias or congenital abnormality, ochronosis, acromegaly, hemochromatosis, Wilson's disease, primary osteochondromatosis, juvenile chronic arthritis with continued activity in adulthood, heritable disorders (e.g. hypermobility). Patients with secondary osteoarthritis following menisectomy or injuries of a collateral or cruciate ligament are not excluded.
- Presence or history of underlying metabolic, endocrine, hematologic, pulmonary, cardiac, blood, renal, hepatic, infectious, psychiatric or gastrointestinal conditions
- Evidence of tuberculosis (TB)
One of the risk factors for TB such as:
- Substance abuse (e.g. injection or non-injection)
- Health-care workers with unprotected exposure to patients who are at high risk of TB
- Patients with TB disease before the identification and correct airborne precautions of the patient
- close contact (i.e. share the same air space in a household or other enclosed environment for a prolonged period (days or weeks, not minutes or hours)) with a person with active pulmonary TB disease.
- Significant medical problems, including but not limited to the following: uncontrolled hypertension,congestive heart failure, uncontrolled diabetes type I and II
- Subjects with evidence of hepatic or blood coagulation disorders (i.e. hemophilia, etc), anemia, idiopathic thrombocytopenic purpura, or gastrointestinal disorder: severe hepatic disease, history of alcohol and drug abuse; disease of gall bladder and pancreas; active peptic ulceration, gastrointestinal bleeding or history of severe gastro-esophageal reflux disease or severe hiatus hernia; inflammatory bowel disease.
- Use of any therapeutic protein drug (e.g. anti-tumor necrosis factor alpha (TNFα) antibody)
- Presence of severe renal function impairment. History of renal trauma, glomerulonephritis, patients with one kidney, or renal failure requiring regular dialysis treatment.
- Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive pregnancy test (serum or urine).
- Subjects with known contra-indications to naproxen (e.g. heart or circulation problems, history of ulcer disease etc.), analgesics, antipyretics, or NSAIDs.
- Disease of the spine or other lower extremity joints which may interfere with the assessment of the target joint.
- Surgery on the knee within the last year. Observational arthroscopy, arthroscopic surgery or lavage of the knee within the last 6 months.
- Use of assistive devices other than a cane (walking stick) or knee brace.
- Subjects who have experienced, any time in the past, asthma, acute rhinitis, nasal polyps, angioneurotic edema, urticaria or other allergic-type reaction after taking acetylsalicylic acid (ASA)/ aspirin or NSAIDs.
- Any history of prior peptic ulcer disease or prior NSAID gastrointestinal complications for the past 5 years.
Other protocol defined inclusion/exclusion criteria may apply.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Potroić
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Part A: Canakinumab
In this ascending dose part, participants received a single intra-articular injection of canakinumab.
The beginning dose was 150 mg, escalating to the 300 mg dose and then to 600 mg.
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Intra-articular injection
Inne nazwy:
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Komparator placebo: Part A: Placebo
Participants received a single intra-articular injection of canakinumab-matching placebo.
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Intra-articular injection
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Eksperymentalny: Part B: Canakinumab
Participants received a single intra-articular injection of canakinumab on Day 1 and naproxen matching placebo tablets orally twice daily for 12 weeks.
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Intra-articular injection
Inne nazwy:
Tablets for oral administration
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Komparator placebo: Part B: Placebo
Participants received a single intra-articular injection of canakinumab matching placebo on Day 1 and naproxen matching placebo tablets orally twice daily for 12 weeks.
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Intra-articular injection
Tablets for oral administration
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Aktywny komparator: Part B: Naproxen
Participants received a single intra-articular injection of canakinumab matching placebo on Day 1 and naproxen 500mg tablets orally twice daily for 12 weeks.
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Intra-articular injection
Tablets for oral administration
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Part A: Number of Participants With Intolerance Events
Ramy czasowe: Baseline to Day 3
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An intolerance event is defined as an acute inflammatory reaction, characterized by a 30 mm increase in pain (on a 100 mm visual analog scale (VAS) and associated with a new or worsened synovial fluid effusion within 3 days following the intra-articular (i.a.) injection.
If baseline VAS pain score is ≥ 70 mm, an intolerance event is defined as an increase in pain by 20 mm on a 100 mm VAS associated with new or worsened synovial fluid effusion within 3 days following the i.a.
injection.
If baseline VAS pain score is ≥ 80 mm, an intolerance event is defined as an increase in pain by 10 mm on a 100 mm VAS associated with new or worsened synovial fluid effusion within 3 days following the i.a.
injection.
If baseline pain score is ≥ 90 mm, an intolerance event is defined as the patients experiencing an unspecified increase in pain on a 100 mm VAS associated with new or worsened synovial fluid effusion within 3 days following the i.a.
injection.
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Baseline to Day 3
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Part B: Change From Baseline to Day 4 in Pain Using 100 mm Visual Analog Scale (VAS)
Ramy czasowe: Baseline and Day 4
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After walking for 20 meters, participants were asked to assess the pain in their affected knee on a 100 mm linear visual analog scale ranging from no pain (0 mm) to unbearable pain (100 mm). A negative change from Baseline score indicates improvement. Results are from a Bayesian analysis of covariance (ANCOVA) model, fitting baseline pain VAS score as a covariate, time by treatment as fixed effects, region and subject as random effects. |
Baseline and Day 4
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Part B: Change From Baseline to Week 4 in Western Ontario and McMaster Osteoarthritis Index (WOMAC) Pain Subscale
Ramy czasowe: Baseline and Week 4
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The Western Ontario and McMaster osteoarthritis Index (WOMAC) pain subscale asks patients to rate pain in the index knee joint in the last 48 hours doing different activities on a scale from none (0) to extreme pain (4). The answers are summed and the total pain subscale score ranges from 0 to 20, where higher scores indicate more pain. A negative change from Baseline score indicates improvement. Results are from a Bayesian ANCOVA model, fitting baseline WOMAC pain score as a covariate, time by treatment as fixed effects, region and patient as random effects. |
Baseline and Week 4
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Part B: Change From Baseline in Pain Using 100 mm Visual Analog Scale (VAS)
Ramy czasowe: Baseline and Weeks 4, 8 and 12
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After walking for 20 meters, participants were asked to assess the pain in their affected knee on a 100 mm linear visual analog scale ranging from no pain (0 mm) to unbearable pain (100 mm). Results are from a Bayesian ANCOVA model, fitting baseline pain VAS score as a covariate, time by treatment as fixed effects, region and patient as random effects. |
Baseline and Weeks 4, 8 and 12
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Part B: Percentage of Responders in the Pain 100 mm Visual Analog Scale (VAS)
Ramy czasowe: Baseline, Day 4, Weeks 1, 2, 4, 8 and 12
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A responder is defined as a participant with a 50% or greater reduction from baseline on the VAS scale for pain assessment.
After walking for 20 meters, participants were asked to assess the pain in their affected knee on a 100 mm linear visual analog scale ranging from no pain (0 mm) to unbearable pain (100 mm).
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Baseline, Day 4, Weeks 1, 2, 4, 8 and 12
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Part B: Change From Baseline in WOMAC Pain, Stiffness and Physical Function Subscales
Ramy czasowe: Baseline and Weeks 4, 8 and 12
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The WOMAC consists of 3 subscales: The Pain subscale asks patients to rate pain in the index knee joint in the last 48 hours during walking, using stairs, in bed, sitting or lying, and standing on a scale from none (0) to extreme pain (4). The answers are summed and the total pain subscale score ranges from 0-20. The Stiffness subscale assesses stiffness in the index knee joint during the last 48 hours doing different activities on a scale from none (0) to extreme stiffness (4). The total stiffness subscale score ranges from 0-8. The Physical Function subscale assesses difficulty performing daily physical activities during the last 48 hours on a scale from none (0) to extreme difficulty (4). The total physical function subscale score ranges from 0-68. Higher scores indicate more pain/stiffness/difficulty. Results are from a Bayesian ANCOVA model, with baseline WOMAC score as a covariate, time by treatment as fixed effects, region and patient as random effects. |
Baseline and Weeks 4, 8 and 12
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Part B: Proportion of Participants Who Used Rescue Analgesic During Study
Ramy czasowe: Day 4, Weeks 1, 2, 4, 8 and 12
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Participants were permitted to take oral rescue medication (Acetaminophen ≤ 4 gram/day) up until 24 hours of a scheduled assessment visit during the 12-week treatment period.
The estimates shown are the Kaplan-Meier estimates of the proportion of participants that took rescue medication.
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Day 4, Weeks 1, 2, 4, 8 and 12
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Patient's Global Assessment of Response to Treatment on Day 4
Ramy czasowe: Day 4
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Participants made a global assessment of their response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Day 4
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Patient's Global Assessment of Response to Treatment at Week 2
Ramy czasowe: Week 2
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Participants made a global assessment of their response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 2
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Patient's Global Assessment of Response to Treatment at Week 4
Ramy czasowe: Week 4
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Participants made a global assessment of their response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 4
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Patient's Global Assessment of Response to Treatment at Week 8
Ramy czasowe: Week 8
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Participants made a global assessment of their response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 8
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Patient's Global Assessment of Response to Treatment at Week 12
Ramy czasowe: Week 12
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Participants made a global assessment of their response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 12
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Part B: Physician's Global Assessment of Response to Treatment at Day 4
Ramy czasowe: Day 4
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The study physician made a global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Day 4
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Part B: Physician's Global Assessment of Response to Treatment at Week 2
Ramy czasowe: Week 2
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The study physician made a global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 2
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Part B: Physician's Global Assessment of Response to Treatment at Week 4
Ramy czasowe: Week 4
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The study physician made a global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 4
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Part B: Physician's Global Assessment of Response to Treatment at Week 8
Ramy czasowe: Week 8
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The study physician made a global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 8
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Part B: Physician's Global Assessment of Response to Treatment at Week 12
Ramy czasowe: Week 12
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The study physician made a global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Poor, Very Poor.
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Week 12
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Maximum Observed Plasma Concentration of Canakinumab (Cmax)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Time to Reach the Maximum Observed Plasma Concentration of Canakinumab (Tmax)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Area Under the Concentration Time Curve up to the Last Measurable Concentration (AUClast)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Area Under the Concentration Time Curve From Time Zero to Infinity AUC(0-inf)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Terminal Phase Half-life (t1/2) of Canakinumab
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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The time it takes for the concentration level of canakinumab to fall to 50% of the original value.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Apparent Clearance of Canakinumab From Plasma (CL/F)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Apparent Volume of Distribution During Terminal Phase (Vz/F)
Ramy czasowe: Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Day 1, pre-dose and 1, 3, 6 and 8 hours post-dose (Part A only), Day 2, 4, 8, 15, 29, 57, 85 and 126.
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Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Choroby stawów
- Choroby układu mięśniowo-szkieletowego
- Choroby reumatyczne
- Artretyzm
- Zapalenie kości i stawów
- Fizjologiczne skutki leków
- Molekularne mechanizmy działania farmakologicznego
- Agenty obwodowego układu nerwowego
- Inhibitory enzymów
- Środki przeciwbólowe
- Agenci systemu sensorycznego
- Środki przeciwzapalne, niesteroidowe
- Środki przeciwbólowe, nie narkotyczne
- Środki przeciwzapalne
- Środki przeciwreumatyczne
- Inhibitory cyklooksygenazy
- Czynniki immunologiczne
- Środki tłumiące dnę moczanową
- Przeciwciała, monoklonalne
- Naproksen
Inne numery identyfikacyjne badania
- CACZ885C2201
- 2009-015017-48 (Numer EudraCT)
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