Condition: Idiopathic Pulmonary Fibrosis · Sponsor: Endeavor Biomedicines, Inc.
The purposes of this study are to: 1. evaluate potential interactions between taladegib (ENV-101) and current standard-of-care (SOC) therapies for idiopathic pulmonary fibrosis (IPF), including nintedanib and pirfenidone, and 2. more fully characterize the pharmacokinetics (PK) of taladegib (i.e., how the body absorbs, distributes, metabolizes and excretes taladegib). This study will enroll 4 cohorts (groups) of participants. Each cohort will experience a different duration of treatment and sequestering (being housed) at the clinical site, followed by a 14-day follow-up period for safety evaluation. The longest duration of treatment for any cohort is 30 days.
This description comes directly from the study's public registry record.
Endeavor Clinical Trials · 1-858-727-3199 · ebmclinical@endeavorbiomedicines.com
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| Research Site | Brisbane, Queensland, Australia | Recruiting |
| Research Site | Melbourne, Victoria, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07454291