NCT06440746RecruitingPhase 2
A Randomized, Double-blind, Parallel-group, Placebo-controlled, Multicenter Phase 2/3 Study of Efficacy and Safety of Olokizumab in Subjects With Progressive Fibrosing Interstitial Lung Diseases
R-Pharm International, LLC33 sites in 1 country138 target enrollmentStarted: August 23, 2023Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Phase 2
- Status
- Recruiting
- Sponsor
- R-Pharm International, LLC
- Enrollment
- 138
- Locations
- 33
- Primary Endpoint
- The rate of forced vital capacity (FVC)
Study Overview
Brief Summary
The purpose of this study is to evaluate efficacy and safety of olokizumab (OKZ) compared to placebo in patients progressive fibrosing Interstitial lung diseases (ILD).
Detailed Description
This is a phase 2/3 study with double-blind parallel-group adaptive design.
The study will include the following periods:
- Screening period (4 weeks) Screening period (before the first administration of the test drug). Before being included in the study, patients will be provided with complete information about this clinical trial and signs the Informed consent Form (IF). After that the researcher will decide whether or not the patient can be randomized into the study.
- Double-blind Treatment period (48 weeks). Following the completion of a Treatment period, all patients will be enrolled in Follow-up Period (FU).
- Follow-up Period (24 weeks). During the FU Period, patients will visit study sites after 4,12 and 24 weeks after the end of the Treatment Period to complete FU-1 (Week 52), FU-2 (Week 60) and FU-3 (Week 72) visits.
The overall study duration for the patients will be approximately 76 weeks (including the 4 weeks screening period)
The analysis will be conducted in two sequential steps:
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Care Provider, Investigator)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •The patient has signed the Informed Consent Form
- •Progressive fibrosing ILD confirmed by high-resolution computed tomography (HRCT) documented evidence of >10% lung tissue affected at Screening:
- •A. Patients with an usual interstitial pneumonia (UIP) -like radiological pattern described in the 2022 American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association guidelines for the management Idiopathic pulmonary fibrosis (IPF) that do not have an identified primary condition
- •В. Patients with progressive interstitial pneumonia with autoimmune features (IPAF) as defined in the American Thoracic Society/European Respiratory Society Statement, 2015
- •С. Patients with progressive lung fibrosis associated with different disorders (c) such as systemic connective tissue diseases, chronic fibrosin hypersensitivity pneumonitis (HP), idiopathic non-specific interstitial pneumonia (iNSIP) or sarcoidosis.
- •Disease progression will be established based on a combination of criterion (I)(a) and criterion (II) or criterion (III)(b)
- •I. Clinically significant decrease in FVC% predicted defined as absolute decrease of ≥ 5% within 12 months prior to screening or an absolute decrease DLCO (corrected for hemoglobin) of ≥10% predicted within 12 months prior to screening.
- •II. Worsening respiratory symptoms without an alternative explanation within 12 months prior to screening.
- •III. Increased area affected with fibrosis on chest HRCT (b) (according to the 2022 American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association guidelines) within 24 months prior to screening.
- •To assess this criterion (I), patient's pulmonary function test (PFT) results obtained within 12 months prior to screening must available. If data from multiple PFTs are available, the earliest results must be used for assessment.
- •Patients' results of at least one chest HRCT investigation performed no earlier than 24 months before randomization must be available for review. If results of multiple HRCT examinations are available, patient eligibility must be based on the earliest results.
- •stable course of the main disease not requiring a change in maintenance treatment.
- •ILD duration of no more than 8 years from the onset of respiratory symptoms by the date screening begins.
- •Elevated acute phase reactants at screening not related to other causes:
- •C-reactive protein level ≥6 mg/l or Erythrocyte Sedimentation Rate (ESR) ≥28 millimeters per hour (mm/hour).
- •FVC ≥ 45% and ≤ 80% predicted at screening.
- •Non-Inclusion Criteria:
- •Hemoglobin-corrected DLCO < 30% predicted at screening.
- •Significant airway obstruction at screening defined as a Forced expiratory volume in 1 second (FEV1) / FVC ratio of <70 %.
- •Use of interleukin-6(IL-6 )inhibitors or IL-6 receptor inhibitors except for CoronaVirus Disease2019 (COVID-19) treatment. If those medications are used to treat COVID-19, the last administration of IL-6 inhibitors or IL-6 receptor inhibitors must have occurred at least 6 months prior to screening.
- •Administration of rituximab within less than 12 months prior to screening.
- •Treatment with systemic glucocorticosteroids (GCS) at >10 mg/day calculated for prednisolone; or a change in the dose of GCS within 4 weeks before/during the screening period; or planned dose changes during the trial.
- •A history of bone marrow transplantation, total lymphoid tissue irradiation, or administration of ablative ultra-high doses of cyclophosphamide.
- •Initiation of mycophenolate mofetil or antifibrotic agents (for patients receiving mycophenolate mofetil and/or antifibrotics at study entry) less than 12 months prior to screening.
- •If a patient has been taking antifibrotic drugs for <12 months and ≥6 months, and the spirometry/Diffusion Capacity Of The Lungs For Carbon Monoxide (DLCO) used to assess progression was performed within ±2 weeks of actually starting antifibrotic drugs, the patient may be included in the study
- •Discontinuation of previously prescribed antifibrotic agents within 6 months prior to screening (for patients not receiving antifibrotic drugs at study entry).
- •Participation in any other clinical trial less than 30 days prior to the baseline assessment or less than 5 half-lives of the medication examined in another clinical trial, whichever is longer.
- •Laboratory abnormalities as follows:
- •Alanine Aminotransferase (ALT) or Aspartate Aminotransferase(AST) ≥ 1.5×Upper Limit Normal (ULN)
- •Platelet count <100×10^9/litre (l) (<100000/cubic millimetre (mm^3)
- •Leukocyte count <3.5×10^9/l
- •Absolute neutrophil count <2000×10^6/l (<2000/mm^3).
- •Concurrent malignancy or a history of malignancy within the last 5 years.
- •Any acute infection at screening or exacerbation of a chronic infection, any infection requiring oral antibiotics or antivirals within 4 weeks prior to screening, injection of antimicrobial agents within 6 weeks before randomization, severe or recurrent infections requiring hospital admission within 6 months before randomization.
- •Patients with evidence of disseminated herpes zoster infection, herpes zoster with encephalitis, meningitis, or other forms of herpes zoster infection that do not resolve without treatment and occurred within 6 months prior to screening.
- •Evidence of any other chronic infection (including sepsis, invasive fungal infection, histoplasmosis, osteomyelitis) which, in the opinion of the Investigator, may increase the risk of infectious complications during the trial.
- •Patients with diverticulitis or other symptomatic gastrointestinal diseases that may lead to perforation, including such history (for example, diverticulitis, gastrointestinal perforation, ulcerative colitis).
- •Women of child-bearing potential or men whose partners are women of child-bearing potential who do not want to use highly effective methods of contraception during the trial and for at least 3 months after the last administration of the investigational product.
- •Known hypersensitivity to OKZ or any other component of the product or placebo.
- •History of severe allergic or anaphylactic reactions to human, humanized, or murine monoclonal antibodies.
- •Other protocol-defined non-inclusion criteria apply.
Exclusion Criteria
- Not provided
Arms & Interventions
Arm1:OKZ 64 mg q4w
Experimental
SC injections of OKZ 64 mg q4w
Intervention: Subcutaneous (SC) injections of OKZ 64 milligrams (mg) every 4 weeks (q4w), one injection of 0.4 millilitre (mL) (Drug)
Arm2:Placebo
Placebo Comparator
SC injections of Placebo q4w
Intervention: SC injections of Placebo every 4 weeks (q4w), one injection of 0.4 mL (Drug)
Outcomes
Primary Outcomes
The rate of forced vital capacity (FVC)
Time Frame: 48 weeks
FVC decline rate assessed over 48 weeks of therapy. FVC is the maximum amount of air that can be exhaled when blowing out as fast as possible.
Secondary Outcomes
- Number of patients (in %) with improved pulmonary function(48 weeks)
- Change of Diffusing capacity of the lungs for carbon monoxide (DLCO)(24,48 weeks)
- Change in the values of quantitative assessment of lung fibrosis from baseline(48 weeks)
- Time to progression or death assessed over 48 weeks of treatment(48 weeks)
- Change in FVC from baseline(24, 48 weeks.)
- Change in FVC.% predicted(24,48 weeks)
- Number of patients (in %) with a decrease in FVC(48 weeks)
- Proportion of patients with progression or death(48 weeks)
- Change in Short Form-36 (SF-36) scores from baseline at treatment weeks 24 and 48(24,48 weeks)
- Time to exacerbation over 48 weeks of treatment(48 weeks)
- Proportion of patients with exacerbation at treatment weeks 24 and 48(24,48 weeks)
- Change in Functional Assessment of Chronic Illness Therapy (FACIT)-Dyspnea scores from baseline at treatment weeks 24 and 48(24,48 weeks)
- Change in Modified Medical Research Council ( mMRC) dyspnea score from baseline at treatment weeks 24 and 48(24,48 weeks)
Investigators
Study Sites (33)
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