Drug Search Results
Using advanced filters...
Advanced Search [+]

Cudetaxestat

Alternative Names: Cudetaxestat, bld-0409, bld0409, bld 0409
Clinical Status: Inactive
Latest Update: 2023-04-17
Latest Update Note: News Article

Product Description

Cudetaxestat (BLD-0409) is a non-competitive autotaxin inhibitor with direct anti-fibrotic activity and differentiating characteristics that is expected to enter a planned phase 2 clinical trial in patients with idiopathic pulmonary fibrosis. (Sourced from: https://www.blademed.com/news/august-22-2022/)

Mechanisms of Action: Autotaxin Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Orphan Drug - Scleroderma, General *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Blade Therapeutics
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Idiopathic Pulmonary Fibrosis

Phase 1: Healthy Volunteers|Fatty Liver, Alcoholic|Liver Diseases, Alcoholic|Hepatitis, Chronic|Hepatitis, Alcoholic|Non-alcoholic Steatohepatitis

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

B-0409-104

P1

Completed

Healthy Volunteers

2021-12-16

12%

2022-04-16

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

B-0409-103

P1

Completed

Healthy Volunteers

2021-09-17

50%

2022-05-18

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

B-0409-102

P1

Completed

Healthy Volunteers

2021-08-17

50%

2021-11-11

B-0409-101

P1

Completed

Hepatitis, Alcoholic|Fatty Liver, Alcoholic|Non-alcoholic Steatohepatitis|Hepatitis, Chronic|Liver Diseases, Alcoholic

2020-12-03

50%

2021-06-05

B-0409-201

P2

Unknown status

Idiopathic Pulmonary Fibrosis

2023-12-30

12%

2024-05-02

Primary Endpoints|Treatments|Trial Status