85. Idiopathic interstitial pneumonia Clinical trials / Disease details
Clinical trials : 627 / Drugs : 443 - (DrugBank : 120) / Drug target genes : 99 - Drug target pathways : 212
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | NCT05483907 (ClinicalTrials.gov) | February 21, 2023 | 27/7/2022 | To Evaluate the Efficacy, Safety, and Tolerability of BBT-877 in Patients With IPF | A Phase 2, Randomized, Double-blind, Placebo-controlled, 24-Week Study to Evaluate the Efficacy, Safety, and Tolerability of BBT-877, as Mono- or add-on Therapy, in Patients With Idiopathic Pulmonary Fibrosis (IPF) | Idiopathic Pulmonary Fibrosis | Drug: BBT-877;Drug: Placebo | Bridge Biotherapeutics, Inc. | NULL | Recruiting | 40 Years | N/A | All | 120 | Phase 2 | United States;Australia;Israel |
2 | NCT03830125 (ClinicalTrials.gov) | February 13, 2019 | 31/1/2019 | Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BBT-877 in Healthy Subjects | A Phase 1, 2-Stage, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BBT-877 Following Single and Multiple Ascending Doses in Healthy Adult Subjects | Idiopathic Pulmonary Fibrosis | Drug: BBT-877, Single dose;Drug: Placebo group;Drug: BBT-877, Multiple doses | Bridge Biotherapeutics, Inc. | KCRN Research, LLC | Completed | 19 Years | 55 Years | All | 88 | Phase 1 | United States |