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Be Part of Research - Trial Details - Safety, Pharmacodynamics, and Pharmacokinetics of Orally Administered BLD-2660 in Subjects With IPF

Safety, Pharmacodynamics, and Pharmacokinetics of Orally Administered BLD-2660 in Subjects With IPF

Stopped

Open to: ALL

Age: 45.0 - N/A

Medical Conditions

Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
Fibrosis


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A Phase 2a, Double-Blind, Placebo-Controlled Study to Evaluate Pharmacodynamics, Pharmacokinetics, and Safety of BLD-2660 Administered Orally in Subjects with Idiopathic Pulmonary Fibrosis

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Dec 2019 Sep 2020

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : BLD-2660 - 150 mg capsules '00' size (PO) BID

Intervention Arm Group : Cohort 1a BLD-2660;Cohort 1b BLD-2660;Cohort 2 BLD-2660;Cohort 3 BLD-2660;

Intervention Type : DRUG
Intervention Description : Placebo - 150 mg capsules '00' size (PO) BID

Intervention Arm Group : Cohort 1a Placebo;Cohort 1b Placebo;Cohort 2 Placebo;Cohort 3 Placebo;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Blade Research Site
    London


The study is sponsored by Blade Therapeutics




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Read full details for Trial ID: NCT04244825
Last updated 02 March 2021

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