A Study to Investigate Leramistat in Patients With IPF
a study on Fibrosis Idiopathic Pulmonary Fibrosis
Summary
- Eligibility
- for people ages 40 years and up (full criteria)
- Location
- at UCSF
- Dates
- study startedcompletion around
Description
Summary
To compare the effect of daily oral dosing of leramistat over 12 weeks with placebo in participants aged 40 years or older with idiopathic pulmonary fibrosis (IPF).
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Investigate the Efficacy and Safety of Leramistat in Patients With Idiopathic Pulmonary Fibrosis (IPF)
Details
This will be a Phase 2, double-blind, placebo-controlled, 2-arm, parallel-group, multi-centre study to investigate leramistat treatment of patients aged 40 years or older with IPF. The study is planned to consist of the following parts:
Screening period: 1 to 28 days (Weeks -4 to -1). Treatment period: a 12-week blinded, placebo-controlled treatment period (Weeks 1 to 12).
Follow up period: 56 days (Weeks 13 to 20). All participants will return for a follow-up visit 56 days after their final dose.
Randomization will be stratified by concomitant use of an approved anti-fibrotic drug (nintedanib or pirfenidone) at randomization versus no concomitant use of an approved anti-fibrotic drug at randomization.
Number of Participants: Approximately 150 participants will be enrolled and randomly assigned in a 2:1 ratio to receive either leramistat or matched placebo.
If the participant is receiving nintedanib or pirfenidone treatment, it should be stable for at least 8 weeks prior to study entry and be predicted to remain stable during the course of the study. The maximum duration of participation (including screening period and follow-up) is 24 weeks.
Data Monitoring/Other Committee: A DSMB has been appointed for this study.
Keywords
Idiopathic Pulmonary Fibrosis, IPF, Pulmonary Fibrosis, Fibrosis, Leramistat
Eligibility
You can join if…
Open to people ages 40 years and up
- Diagnosis of IPF based on: a. ATS/ERS/JRS/ALAT guidelines (Raghu, 2022) as confirmed by the investigator based on chest high-resolution computed tomography (hrCT) scan taken within 3 years of Screening and, if available, surgical lung biopsy b. UIP or probable UIP hrCT pattern consistent with the clinical diagnosis of IPF, as confirmed by central review prior to baseline (if indeterminate, hrCT findings of IPF may be confirmed locally by historical biopsy).
- Has an FVC ≥45% of predicted.
- Has a DLCO corrected for hemoglobin ≥25% and ≤80% of predicted.
- Minimum distance on 6MWT of 150 meters.
- Has a FEV1/FVC ratio >0.70.
- If on anti-fibrotics, only the approved treatments of nintedanib or pirfenidone are allowed. Participants must be on a stable dose for at least 8 weeks prior to Visit 1
- Has a life expectancy of at least 12 months (in the opinion of the investigator).
- This list contains only key inclusion criteria.
You CAN'T join if...
- Emphysema ≥50% on hrCT or the extent of emphysema is greater than the extent of fibrosis according to the central reviewer's assessment from the most recent hrCT or if reported by the local reviewer.
- Any current malignancy or a history of malignancy within the previous 5 years prior to screening, with the exception of adequately treated or excised non-metastatic basal cell or squamous cell cancer of the skin or cervical carcinoma in situ.
- Abnormality in heart rate, blood pressure or 12-lead ECG at screening that in the opinion of the Investigator increases the risk of participating in the study.
- Significant history of drug allergy, including to leramistat or excipients, as determined by the Investigator.
- Allergic reaction, anaphylaxis, or other reactions (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis or leukopenia)
- History of opportunistic, chronic, or recurrent infections.
- Participants with chronic obstructive pulmonary disease (COPD) or asthma that:
- require >2 maintenance therapies
- have experienced an exacerbation requiring hospitalization or systemic corticosteroids within 12 months prior to screening.
- This list contains only key exclusion criteria.
Locations
- UCSF Fresno
not yet accepting patients
Fresno California 93701-2302 United States - University of Utah - PPDS
not yet accepting patients
Salt Lake City Utah 84108-1257 United States - Southeastern Research Center
accepting new patients
Winston-Salem North Carolina 27103-4029 United States - Hopital Nord AP-HM
accepting new patients
Marseille France - Hôpital Pasteur II
not yet accepting patients
Nice France - Hôpital Européen Georges Pompidou
not yet accepting patients
Paris France - Hopital Robert Schuman
in progress, not accepting new patients
Vantoux France
Details
- Status
- accepting new patients at some sites,
but this study is not currently recruiting here - Start Date
- Completion Date
- (estimated)
- Sponsor
- Modern Biosciences Ltd
- ID
- NCT05951296
- Phase
- Phase 2 research study
- Study Type
- Interventional
- Participants
- Expecting 150 study participants
- Last Updated