Eosinophilic AsthmaPhase 3NCT01270464
A Study to Evaluate the Efficacy and Safety of Reslizumab (0.3 or 3.0 mg/kg) as Treatment for Patients (12-75 Years of Age) With Eosinophilic Asthma
A Phase 3 study testing Reslizumab in people with Eosinophilic Asthma, run by Teva Branded Pharmaceutical Products R&D, Inc. at 89 sites in 13 countries.
Trial summary
The primary objective of this study is to determine whether reslizumab, at a dosage of 0.3 or 3.0 mg/kg administered once every 4 weeks for a total of 4 doses, is more effective than placebo in improving lung function in patients with eosinophilic asthma as assessed by the overall change from baseline in forced… Read more about this study
- Who is it for?
- Ages 12 to 75 years
- Conditions the study is for
- Eosinophilic Asthma
- What is being tested?
- Reslizumab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 315 participants
- Where
- 89 sitesin 13 countries
- Study dates
- Feb 2011to Sep 2013
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 to 75 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- The patient is male or female, 12 through 75 years of age, with a previous diagnosis of asthma. Patients 12 through 17 years of age are excluded from participating in Argentina.
- The patient has an ACQ score of at least 1.5.
- The patient has airway reversibility of at least 12% to beta-agonist administration at screening.
- The patient is currently taking fluticasone at a dosage of at least 440 μg daily (or equivalent). Patients' baseline asthma therapy regimens (including but not limited to inhaled corticosteroids, leukotriene antagonists, 5-lipoxygenase inhibitors, cromolyn) must be stable for 30 days before screening, and continue without dosage changes throughout study.
- The patient has a blood eosinophil count of at least 400/μL.
- Female patients must be surgically sterile, 2 years postmenopausal, or must have a negative pregnancy test ßHCG at screening (serum) and baseline (urine).
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- Female patients of childbearing potential (not surgically sterile or 2 years postmenopausal), must use a medically accepted method of contraception and must agree to continue use of this method for the duration of the study and for 30 days after the end-of-treatment visit. Acceptable methods of contraception include barrier method with spermicide, abstinence, intrauterine device (IUD), or steroidal contraceptive (oral, transdermal, implanted, and injected).
- Written informed consent is obtained. Patients 12 through 17 years old, where participating, need to provide assent in accordance with local standards.
- Other inclusion criteria apply.
Who cannot join
- The patient has a clinically meaningful comorbidity that would interfere with the study schedule or procedures, or compromise the patient's safety.
- The patient has known hypereosinophilic syndrome (HES).
- The patient has another confounding underlying lung disorder (eg, chronic obstructive pulmonary disease, pulmonary fibrosis, or lung cancer). The patient has other pulmonary conditions with symptoms of asthma and blood eosinophilia (eg, Churg-Strauss syndrome, allergic bronchopulmonary aspergillosis).
- The patient is a current smoker (ie, has smoked within the last 6 months prior to screening).
- The patient has a history of use of systemic immunosuppressive or immunomodulating agents (anti-IgE mAb, methotrexate, cyclosporin, interferon-α, or anti-tumor necrosis factor mAb) within 6 months prior to study entry (screening).
- The patient is currently using systemic corticosteroids (includes use of oral corticosteroids).
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- The patient has a current infection or disease that may preclude assessment of asthma.
- The patient is expected to be poorly compliant with study drug administration, study procedures, or visits.
- The patient has any aggravating factors that are inadequately controlled (eg, gastroesophageal reflux disease).
- The patient has participated in any investigative drug or device study within 30 days prior to screening.
- The patient has participated in any investigative biologics study within 90 days prior to screening.
- The patient has previously received anti-hIL-5 monoclonal antibody (eg, mepolizumab).
- Female patients who are pregnant, or nursing, or, if of childbearing potential and not using a medically accepted, effective method of birth control (e.g. spermicide, abstinence, IUD, or steroidal contraceptive [oral, transdermal, implanted, and injected]) are excluded from this study.
- The patient has a current infection or disease that may preclude assessment of asthma.
- The patient has a history of concurrent immunodeficiency (human immunodeficiency, acquired immunodeficiency syndrome, or congenital immunodeficiency). Patients in Argentina must have documented serology testing for HIV performed during screening.
- Other exclusion criteria apply.
Trial locations and contacts
89 sites in 13 countries.
89 sites in 13 countries
United States26 sites
Teva Investigational Site 12
Anaheim, California
Teva Investigational Site 21
Charleston, South Carolina
Teva Investigational Site 20
Cincinnati, Ohio
Teva Investigational Site 2
Colorado Springs, Colorado
Teva Investigational Site 16
Fort Worth, Texas
Teva Investigational Site 11
Fountain Valley, California
Teva Investigational Site 10
Houston, Texas
Teva Investigational Site 7
Iowa City, Iowa
Teva Investigational Site 24
Largo, Florida
Teva Investigational Site 6
Lilburn, Georgia
Teva Investigational Site 73
Lincoln, Rhode Island
Teva Investigational Site 43
Los Angeles, California
Teva Investigational Site 1
Medford, Oregon
Teva Investigational Site 27
Miami, Florida
Teva Investigational Site 5
Miami, Florida
Teva Investigational Site 8
Omaha, Nebraska
Teva Investigational Site 4
Orange, California
Teva Investigational Site 9
Providence, Rhode Island
Teva Investigational Site 14
San Antonio, Texas
Teva Investigational Site 45
San Antonio, Texas
Teva Investigational Site 3
Savannah, Georgia
Teva Investigational Site 26
Summit, New Jersey
Teva Investigational Site 19
Tallahassee, Florida
Teva Investigational Site 17
Trinity, Florida
Teva Investigational Site 18
Valrico, Florida
Teva Investigational Site 15
Walnut Creek, California
Argentina9 sites
Teva Investigational Site 121
Ciudad Autonoma de Buenos Aire
Teva Investigational Site 126
Ciudad Autonoma de Buenos Aire
Teva Investigational Site 127
Ciudad Autonoma de Buenos Aire
Teva Investigational Site 128
Quilmes-Buenos Aires
Teva Investigational Site 125
Rosario
Teva Investigational Site 123
Rosario-Santa Fe
Teva Investigational Site 120
San Miguel de Tucuman - Tucuma
Teva Investigational Site 122
San Miguel de Tucuman - Tucuma
Teva Investigational Site 124
San Miguel de Tucuman - Tucuma
Brazil9 sites
Teva Investigational Site 146
Belo Horizonte
Teva Investigational Site 150
Florianópolis
Teva Investigational Site 140
Porto Alegre
Teva Investigational Site 143
Porto Alegre
Teva Investigational Site 144
Porto Alegre
Teva Investigational Site 145
Porto Alegre
Teva Investigational Site 147
Porto Alegre - RS
Teva Investigational Site 142
Santo André
Teva Investigational Site 141
São Paulo
Hungary7 sites
Teva Investigational Site 401
Balassagyarmat
Teva Investigational Site 406
Edelény
Teva Investigational Site 400
Miskolc
Teva Investigational Site 404
Mosonmagyaróvár
Teva Investigational Site 403
Sopron
Teva Investigational Site 407
Százhalombatta
Teva Investigational Site 402
Tatabánya
Poland7 sites
Teva Investigational Site 507
Bialystok
Teva Investigational Site 513
Gdansk
Teva Investigational Site 512
Lodz
Teva Investigational Site 505
Lublin
Teva Investigational Site 500
Ostrów Wielkopolski
Teva Investigational Site 502
Sopot
Teva Investigational Site 504
Tarnów
Colombia6 sites
Teva Investigational Site 181
Bogotá
Teva Investigational Site 184
Bogotá
Teva Investigational Site 185
Bogotá
Teva Investigational Site 182
Cali
Teva Investigational Site 180
Floridablanca
Teva Investigational Site 183
Medellín
France5 sites
Teva Investigational Site 343
Grenoble
Teva Investigational Site 342
Marseille
Teva Investigational Site 341
Montpellier
Teva Investigational Site 340
Nantes
Teva Investigational Site 344
Pessac
Mexico5 sites
Teva Investigational Site 203
Distrito Federal
Teva Investigational Site 205
Distrito Federal
Teva Investigational Site 204
Guadalajara, JAL
Teva Investigational Site 200
Hermosillo, Sonora
Teva Investigational Site 202
Tijuana, B.C.
Belgium4 sites
Teva Investigational Site 261
Brussels
Teva Investigational Site 264
Brussels
Teva Investigational Site 260
Ghent
Teva Investigational Site 263
Liège
Canada4 sites
Teva Investigational Site 103
Calgary
Teva Investigational Site 101
Montreal
Teva Investigational Site 104
Newmarket
Teva Investigational Site 105
Windsor
Israel3 sites
Teva Investigational Site 422
Petah Tikva
Teva Investigational Site 421
Rehovot
Teva Investigational Site 420
Tel Aviv
Sweden3 sites
Teva Investigational Site 602
Gothenburg
Teva Investigational Site 600
Lund
Teva Investigational Site 601
Malmö
About this study
Official title: A 16-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (0.3 or 3.0 mg/kg) as Treatment for Patients (12-75 Years of Age) With Eosinophilic Asthma
The primary objective of this study is to determine whether reslizumab, at a dosage of 0.3 or 3.0 mg/kg administered once every 4 weeks for a total of 4 doses, is more effective than placebo in improving lung function in patients with eosinophilic asthma as assessed by the overall change from baseline in forced expiratory volume in 1 second (FEV1).
- Conditions
- Eosinophilic Asthma
- Being tested
- Reslizumab, Placebo
- Medical subject headings
- Pulmonary Eosinophilia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ReslizumabDrug
Also called Cinquil, humanized monoclonal antibody, CEP-38072
3.0 mg/kg or 0.3 mg/kg doses administered intravenously (iv) by qualified site personnel once every 4 weeks, for a total of 4 doses.
PlaceboDrug
Placebo administered by iv infusion by qualified study personnel every 4 weeks for a total of 4 doses.
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | Placebo administered intravenously (iv) once every 4 weeks, for a total of 4 doses. Receives: Drug: Placebo |
| Reslizumab - 0.3 mg/kg | Experimental | 0.3 mg/kg, administered intravenously (iv) once every 4 weeks, for a total of 4 doses Receives: Drug: Reslizumab |
| Reslizumab - 3.0 mg/kg | Experimental | 3.0 mg/kg, administered intravenously (iv) once every 4 weeks, for a total of 4 doses. Receives: Drug: Reslizumab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline In Forced Expiratory Volume In 1 Second (FEV1) Over 16 Weeks Using Mixed Model for Repeated Measures
FEV1 is a standard measurement of air movement in the lungs of patients with asthma obtained from pulmonary function tests. It is the volume of air expired in the first second of a forced expiration using a spirometer. The during treatment (weeks 4, 8, 12 and 16) average FEV1 was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Positive change from baseline scores indicate improvement in asthma control.
Measured: Day 0 (baseline, pre-dose), Weeks 4, 8, 12 and 16
Secondary outcomes (13)
Change From Baseline in Forced Vital Capacity (FVC) Over 16 Weeks Using Mixed Model for Repeated Measures
The FVC is the volume of air that can be forcibly blown out after full inspiration, measured in liters. The during treatment (weeks 4, 8, 12 and 16) average FVC was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Forced Expiratory Flow at 25% to 75% Forced Vital Capacity (FEF 25%-75%) Over 16 Weeks Using Mixed Model for Repeated Measures
The FEF 25%-75% is the force expiratory flow at 25% to 75% of the Forced Vital Capacity (FVC). The during treatment (weeks 4, 8, 12 and 16) average FEF 25%-75% was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in % Predicted Expiratory Volume In 1 Second (FEV1) at Week 16 and at Endpoint
The percent predicted FEV1 is the ratio of the volume of air expired in the first second of a forced expiration to the patient's predicted FEV based on a similar population without asthma. Endpoint =week 16 or early withdrawal.
Measured: Day 1 (baseline, pre-dose), Week 16, endpoint
Change From Baseline in Asthma Control Questionnaire (ACQ) Over 16 Weeks Using Mixed Model for Repeated Measures
The ACQ is a 7-item instrument that measures asthma control (Juniper et al 1999). Six questions are self-assessments; the seventh item, completed by a member of the study staff, is the result of the patient's FEV1 measurement. Each item has 7 possible answers on a scale of 0 to 6, and the total score is the mean of all responses (the total scale is therefore 0-6). A higher score is an indication of poorer asthma control. The during treatment (weeks 4, 8, 12 and 16) average ACQ was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Negative change from baseline scores indicate improvement in asthma control.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Asthma Quality of Life Questionnaire (AQLQ) at Week 16 or at Last Observed Value
The AQLQ is a 32-item instrument administered as a self-assessment (Juniper et al 1992). The questionnaire is divided into 4 domains: activity limitation, symptoms, emotional function, and environmental stimuli. Patients were asked to recall their experiences during the last 2 weeks and to respond to each question on a 7-point scale (1=severe impairment, 7=no impairment). The overall AQLQ score is the mean of all 32 responses. Five of the activity questions were "patient-specific," which means that each patient identified and scored 5 activities in which the patient was limited by asthma; these 5 activities were identified at the first visit and retained for all subsequent follow-up visits.
Positive change from baseline scores indicate improvement in quality of life. The AQLQ score was only assessed once during the study at week 16 or at early withdrawal, i.e. last postbaseline assessment if within 3 to 5 weeks of the last dose of study drug.
Measured: Day 1 (baseline, pre-dose), Week 16 or last observed value
Change From Baseline in Asthma Symptom Utility Index (ASUI) Over 16 Weeks Using Mixed Model for Repeated Measures
The ASUI is an 11-item instrument designed to assess the frequency and severity of asthma symptoms and side effects, weighted by patient preferences (Revicki et al 1998). ASUI is a utility score that ranges from 0 to 1, with higher values indicating better asthma control. The during treatment (weeks 4, 8, 12 and 16) average ASUI was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Positive change from baseline values indicate improvement in asthma symptoms. Information was obtained from questionnaire about asthma symptoms.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Short-Acting Beta-Agonist (SABA) Use Over 16 Weeks Using Mixed Model for Repeated Measures
SABA are used for quick relief of asthma symptoms. To measure SABA use, at each clinical visit patients were asked to recall their usage of SABA therapy within the last 3 days of the scheduled visit. If usage was confirmed, the number of puffs used was recorded. For the purpose of summaries, an average daily usage was evaluated by dividing the total number of puffs recorded over 3 days by 3.
The during treatment (weeks 4, 8, 12 and 16) average SABA use was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Negative change from baseline scores indicate improvement in asthma control.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Blood Eosinophil Count Over 16 Weeks Using Mixed Model for Repeated Measures
Blood eosinophil counts were measured using a standard complete blood count (CBC) with differential blood test at each scheduled visit, and from all patients experiencing a serious adverse event, an adverse event leading to withdrawal, or an exacerbation of asthma symptoms. The during treatment (weeks 4, 8, 12 and 16) average eosinophil counts were estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements.
Negative change from baseline values correlate to reduced asthma severity.
Measured: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Participants With Adverse Events
An adverse event was defined in the protocol as any untoward medical occurrence that develops or worsens in severity during the conduct of a clinical study and does not necessarily have a causal relationship to the study drug. Severity was rated by the investigator on a scale of mild, moderate and severe, with severe= an inability to carry out usual activities. Relation of AE to treatment was determined by the investigator. Serious AEs include death, a life-threatening adverse event, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant disability or incapacity, a congenital anomaly or birth defect, OR an important medical event that jeopardized the patient and required medical intervention to prevent the previously listed serious outcomes. The last postbaseline value for approximately 10 patients in each treatment group is the 90-day follow-up visit post end-of-treatment (approx. Week 29).
Measured: Day 1 (post-dose) to Week 29
Participants With Treatment-Emergent Potentially Clinically Significant (PCS) Abnormal Lab Values
Data represents participants with potentially clinically significant (PCS) abnormal serum chemistry, hematology (except for eosinophil values), and urinalysis values.
Significance criteria:
- Blood urea nitrogen: >=10.71 mmol/L
- Creatinine: >=177 μmol/L
- Uric acid: M>=625, F>=506 μmol/L
- GGT = gamma-glutamyl transpeptidase: >= 3*upper limit of normal. Normal range is 5-49 U/L.
- Total bilirubin: >=34.2 μmol/L
- White blood cells: <=3.0 10^9/L
- Hemoglobin: M<=115, F<=95 g/dL
- Hematocrit: M<0.37, F<0.32 %
- Platelets: >=700 10^9/L
- Absolute neutrophil count: <=1.0 10^9/L
- Urinalysis: blood, glucose, ketones and total protein: >=2 unit increase from baseline
The last postbaseline value for approximately 10 patients in each treatment group is the 90-day follow-up visit post end-of-treatment (approx. Week 29).
Measured: Day 2 to Week 29
Participants With Treatment-Emergent Potentially Clinically Significant (PCS) Vital Signs Values
Data represents participants with potentially clinically significant (PCS) vital sign values.
Significance criteria
- Sitting pulse - high: >100 and increase of >= 30 beats/minute
- Sitting pulse - low: <50 and decrease of >=30 beats/minute
- Sitting diastolic blood pressure: >100 and increase of >=12 mmHg
- Respiration rate: >24 and increase of >=10 breaths/minute
- Body temperature: <96.5° Fahrenheit or <35.8° Celsius
The last postbaseline value for approximately 10 patients in each treatment group is the 90-day follow-up visit post end-of-treatment (approx. Week 29).
Measured: Day 2 to Week 29
Shifts From Baseline to Endpoint in Electrocardiogram Findings
Participant counts in each category of shift from baseline to endpoint of ECG finding. Findings summarized as normal or abnormal.
Measured: Weeks -4 to -2 (Screening Visit), Week 16
Participants With a Positive Anti-Reslizumab Antibody Status at Baseline, Week 8, Week 16, Endpoint, and Overall
Counts of participants with a positive anti-drug antibody (ADA) response during treatment is offered for the two experimental treatment arms. Blood samples were collected for determination of ADAs before study drug infusion at baseline, visit 4 (week 8), and at visit 6 (week 16: EOT or early withdrawal) from patients in all 3 treatment groups (ie, placebo, 0.3 mg/kg reslizumab, and 3.0 mg/kg reslizumab); however, only the blood samples drawn from patients treated with either 0.3 mg/kg reslizumab or 3.0 mg/kg reslizumab were analyzed. Serum samples from patients who were treated with reslizumab were analyzed for ADA by Teva (Teva Biopharmaceuticals USA, Rockville, MD) using a validated homogeneous solution-based bridging enzyme-linked immunosorbent assay (ELISA).
Endpoint =week 16 or early withdrawal.
Measured: Day 1 (pre-dose), week 8, 16 and endpoint
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jan 2011 (estimated)
- Study startFeb 2011
- Primary completionSep 2013
- Study completionSep 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Eosinophilic AsthmaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 315 participants (actual)
Sponsor and investigators
- Lead sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Sponsor's Medical Expert, Senior Director - Worldwide Clinical Research, MD, Study director, Cephalon
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01270464
- Sponsor's protocol ID
- C38072/3081
- Other IDs
- 2010-023342-67
- Status last verified
- Apr 2016
- First submitted
- 29 Dec 2010
- Last updated
- 6 Jun 2016
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Publications
Bjermer L, Lemiere C, Maspero J, Weiss S, Zangrilli J, Germinaro M. Reslizumab for Inadequately Controlled Asthma With Elevated Blood Eosinophil Levels: A Randomized Phase 3 Study. Chest. 2016 Oct;150(4):789-798. doi: 10.1016/j.chest.2016.03.032. Epub 2016 Apr 4.
PubMed 27056586
Study at a glance
From the registry record, last updated by the sponsor on 6 Jun 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A 16-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (0.3 or 3.0 mg/kg) as Treatment for Patients (12-75 Years of Age) With Eosinophilic Asthma
- ClinicalTrials.gov ID
- NCT01270464
- Acronym / sponsor ID
- C38072/3081
- Conditions
- Eosinophilic Asthma
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 315 participants (actual)
- Lead sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.Industry (pharma, biotech, devices)
- Study start
- Feb 2011
- Primary completion
- Sep 2013 (actual)
- Study completion
- Sep 2013 (actual)
- First posted
- 5 Jan 2011 (estimated)
- Results
- Posted 6 Jun 2016
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of this study is to determine whether reslizumab, at a dosage of 0.3 or 3.0 mg/kg administered once every 4 weeks for a total of 4 doses, is more effective than placebo in improving lung function in patients with eosinophilic asthma as assessed by the overall change from baseline in forced expiratory volume in 1 second (FEV1).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Drug: PlaceboPlacebo administered intravenously (iv) once every 4 weeks, for a total of 4 doses. |
| Reslizumab - 0.3 mg/kg | Experimental | Drug: Reslizumab0.3 mg/kg, administered intravenously (iv) once every 4 weeks, for a total of 4 doses |
| Reslizumab - 3.0 mg/kg | Experimental | Drug: Reslizumab3.0 mg/kg, administered intravenously (iv) once every 4 weeks, for a total of 4 doses. |
Who may qualify
- Ages
- 12 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (9 listed)
- The patient is male or female, 12 through 75 years of age, with a previous diagnosis of asthma. Patients 12 through 17 years of age are excluded from participating in Argentina.
- The patient has an ACQ score of at least 1.5.
- The patient has airway reversibility of at least 12% to beta-agonist administration at screening.
- The patient is currently taking fluticasone at a dosage of at least 440 μg daily (or equivalent). Patients' baseline asthma therapy regimens (including but not limited to inhaled corticosteroids, leukotriene antagonists, 5-lipoxygenase inhibitors, cromolyn) must be stable for 30 days before screening, and continue without dosage changes throughout study.
- The patient has a blood eosinophil count of at least 400/μL.
Key exclusion criteria (16 listed)
- The patient has a clinically meaningful comorbidity that would interfere with the study schedule or procedures, or compromise the patient's safety.
- The patient has known hypereosinophilic syndrome (HES).
- The patient has another confounding underlying lung disorder (eg, chronic obstructive pulmonary disease, pulmonary fibrosis, or lung cancer). The patient has other pulmonary conditions with symptoms of asthma and blood eosinophilia (eg, Churg-Strauss syndrome, allergic bronchopulmonary aspergillosis).
- The patient is a current smoker (ie, has smoked within the last 6 months prior to screening).
- The patient has a history of use of systemic immunosuppressive or immunomodulating agents (anti-IgE mAb, methotrexate, cyclosporin, interferon-α, or anti-tumor necrosis factor mAb) within 6 months prior to study entry (screening).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ReslizumabAlso: Cinquil, humanized monoclonal antibody, CEP-380723.0 mg/kg or 0.3 mg/kg doses administered intravenously (iv) by qualified site personnel once every 4 weeks, for a total of 4 doses. | Drug | Reslizumab - 0.3 mg/kg, Reslizumab - 3.0 mg/kg |
| PlaceboPlacebo administered by iv infusion by qualified study personnel every 4 weeks for a total of 4 doses. | Drug | Placebo |
Primary outcome
Change From Baseline In Forced Expiratory Volume In 1 Second (FEV1) Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 0 (baseline, pre-dose), Weeks 4, 8, 12 and 16
FEV1 is a standard measurement of air movement in the lungs of patients with asthma obtained from pulmonary function tests. It is the volume of air expired in the first second of a forced expiration using a spirometer. The during treatment (weeks 4, 8, 12 and 16) average FEV1 was estimated using a mixed-effect model for repeated measures (MMRM) with fixed effects (treatment, stratification factors, sex, visit, interaction of treatment and visit), covariates (height, baseline value), and patient as the random effect for the repeated measurements. Positive change from baseline scores indicate improvement in asthma control.
13 secondary outcomes
Change From Baseline in Forced Vital Capacity (FVC) Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Forced Expiratory Flow at 25% to 75% Forced Vital Capacity (FEF 25%-75%) Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in % Predicted Expiratory Volume In 1 Second (FEV1) at Week 16 and at Endpoint
Time frame: Day 1 (baseline, pre-dose), Week 16, endpoint
Change From Baseline in Asthma Control Questionnaire (ACQ) Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Asthma Quality of Life Questionnaire (AQLQ) at Week 16 or at Last Observed Value
Time frame: Day 1 (baseline, pre-dose), Week 16 or last observed value
Change From Baseline in Asthma Symptom Utility Index (ASUI) Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Short-Acting Beta-Agonist (SABA) Use Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Change From Baseline in Blood Eosinophil Count Over 16 Weeks Using Mixed Model for Repeated Measures
Time frame: Day 1 (baseline, pre-dose), Weeks 4, 8, 12, 16
Participants With Adverse Events
Time frame: Day 1 (post-dose) to Week 29
Participants With Treatment-Emergent Potentially Clinically Significant (PCS) Abnormal Lab Values
Time frame: Day 2 to Week 29
Participants With Treatment-Emergent Potentially Clinically Significant (PCS) Vital Signs Values
Time frame: Day 2 to Week 29
Shifts From Baseline to Endpoint in Electrocardiogram Findings
Time frame: Weeks -4 to -2 (Screening Visit), Week 16
Participants With a Positive Anti-Reslizumab Antibody Status at Baseline, Week 8, Week 16, Endpoint, and Overall
Time frame: Day 1 (pre-dose), week 8, 16 and endpoint
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jun 2016.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 27056586Bjermer L, Lemiere C, Maspero J, Weiss S, Zangrilli J, Germinaro M. Reslizumab for Inadequately Controlled Asthma With Elevated Blood Eosinophil Levels: A Randomized Phase 3 Study. Chest. 2016 Oct;150(4):789-798. doi: 10.1016/j.chest.2016.03.032. Epub 2016 Apr 4.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sponsor's Medical Expert, Senior Director - Worldwide Clinical Research, MD study director
Cephalon
89 sites in 13 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Reslizumab in people with Eosinophilic Asthma, run by Teva Branded Pharmaceutical Products R&D, Inc. at 89 sites in 13 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Jun 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 89 sites in United States, Argentina, Brazil, Hungary, Poland and 8 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 6 Jun 2016). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change From Baseline In Forced Expiratory Volume In 1 Second (FEV1) Over 16 Weeks Using Mixed Model for Repeated Measures (time frame: Day 0 (baseline, pre-dose), Weeks 4, 8, 12 and 16). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01270464, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Jun 2016.