Trial | NCT03949530  Report issue

Title

A Study of Safety & Blood Levels of IDL-2965 in Healthy Subjects and Patients With a Special Type of Pulmonary Fibrosis
IDL-2965 - A Phase I, Randomized, Double-blind, Placebo-controlled, Single and Multiple Oral Dose, Safety, Tolerability, and Pharmacokinetic Study in Healthy Subjects and Subjects With Idiopathic Pulmonary Fibrosis (IPF)

  • Phase

    Phase 1

  • Study Type

    Interventional

  • Status

    Terminated

  • Study Participants

    6
The purpose of this study is to test the safety and tolerability of the drug candidate IDL-2965 and to see how it is absorbed, processed, and removed by the body.
IDL-2965 is an oral integrin antagonist antifibrotic being studied as a potential treatment for IPF and Nonalcoholic Steatohepatitis (NASH). This double-blind, randomized, placebo-controlled, single and multiple oral dose study will be conducted in 3 parts. Part A will comprise a single-dose, sequential-group design in healthy subjects, incorporating a food-effect evaluation. Part B will consist of a multiple-dose, sequential-group design in healthy subjects. Part C will be a multiple-dose, sequential-group design in subjects with IPF.
Study Started
Apr 16
2019
Primary Completion
Mar 29
2020
Study Completion
Mar 29
2020
Last Update
Aug 04
2020

Drug IDL-2965 Oral Capsule

Investigational drug

Drug Placebos

Placebo

IDL-2965 Oral Capsule Experimental

IDL-2965 oral capsule, single and multiple doses

Placebo Oral Capsule Placebo Comparator

Placebo oral capsule, single and multiple doses

Criteria 

Inclusion Criteria:

Healthy subjects:

• Male and female subjects aged between 18 and 60 years, with a body mass index between 18.0 and 32.0 kg/m2.

IPF subjects:

Male and female subjects over 40 years of age.
Diagnosis of idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis has been stable for at least 3 months.

Exclusion Criteria:

Healthy subjects and IPF subjects:

Significant history or clinical manifestation of any disease/disorder, other than IPF.
History of significant hypersensitivity, intolerance, or allergy to any drug compound
Poor peripheral venous access
Use or intend to use any medications, tobacco or nicotine containing products or electronic cigarettes.
History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs

IPF subjects:

• Pulmonary function tests and other diagnostic procedures inconsistent with diagnosis of idiopathic pulmonary fibrosis.
No Results Posted