Phase 2 Study Design and Analysis Approach for BBT-877: An Autotaxin Inhibitor Targeting Idiopathic Pulmonary Fibrosis
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Introduction
Proof-of-concept (POC) studies are vital in determining the feasibility of further drug development, primarily by assessing preliminary efficacy signals with credible endpoints. However, traditional POC studies in idiopathic pulmonary fibrosis (IPF) can suffer from low credibility due to small sample sizes and short durations, leading to non-replicable results in larger Phase III trials. To address this, we are conducting a 24-week POC study with 120 patients with IPF, using a statistically supported sample size and incorporating exploratory computed tomography (CT)-based imaging biomarkers, to support decision making in the case of non-significant primary endpoint results. This approach aims to provide data to enable a robust decision-making process for advancing clinical development of BBT-877.
Methods and analysis
In this phase II, double-blind, placebo-controlled study, approximately 120 patients with IPF will be randomized in a 1:1 ratio to receive placebo or 200mg of BBT-877 twice daily over 24 weeks, with stratification according to background use of an antifibrotic treatment (pirfenidone background therapy, nintedanib background therapy or no background therapy). The primary endpoint is absolute change in FVC (mL) from baseline to week 24. Key secondary endpoints include change from baseline to week 24 in % predicted FVC, diffusing capacity of the lung for carbon monoxide, 6-minute walk test, patient-reported outcomes, pharmacokinetics and safety, and tolerability. Key exploratory endpoints include eLung-based CT evaluation and biomarker-based assessment of pharmacodynamics.
Ethics and Dissemination
This study is being conducted following the Declaration of Helsinki principles, Good Clinical Practice guidance, applicable local regulations, and local ethics committees. An independent data monitoring committee unblinded to individual subject treatment allocation will evaluate safety and efficacy data on a regular basis throughout the study. The results of this study will be presented at scientific conferences and peer-review publications.
Trial Registration Number
NCT05483907
Key Message
What is already known on this topic
Idiopathic pulmonary fibrosis (IPF) is characterized by progressive fibrosis, a high mortality rate and few effective treatment options. Proof of concept studies in IPF have not always translated into successful phase III clinical trials.
What this study adds
A description of the rationale, study design, methods, and analysis plan for a phase II, double-blind, placebo-controlled study of BBT-877 in patients with IPF, either alone or in addition to background antifibrotic treatment (nintedanib or pirfenidone).
How this study might affect research, practice, or policy
This phase II study design is expected to influence future research methodologies and clinical trial practices by providing a robust framework for studying IPF. Additionally, once the ongoing trial with BBT-877 is completed, the research methods will ensure credibility of the findings and will inform future clinical trial design.
