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RLA-23174

Alternative Names: RLA-23174, RLA 23174, RLA23174
Latest Update: None
Latest Update Note: None

Product Description

RLA-23174 is a new small molecule allosteric inhibitor of HIPK2 and a potential first-in-class treatment for pan-organ fibrosis. RLA-23174 inhibits the TGF-beta/Smad3 signaling pathway by affecting the interaction between HIPK2 and Smad3, without inhibiting the kinase activity of HIPK2 or TGF-beta receptor systems. Therefore, RLA-23174 exerts anti-fibrotic effects by reducing TGF-beta signaling without serious adverse effects caused by complete HIPK2 or TGF-beta signaling blockade. Preclinical studies have shown that RLA-23174 has superior anti-fibrotic effects, significant in vivo activity, excellent pharmacokinetic properties in animals, and a good safety profile. RLA-23174 demonstrates good druggability and excellent development potential. (Sourced from: https://www.prnewswire.com/news-releases/rila-therapeutics-announces-dosing-of-first-cohort-in-phase-1-clinical-trial-of-rla-23174-a-first-in-class-hipk2-allosteric-inhibitor-for-treatment-of-chronic-kidney-disease-and-fibrosis-302150159.html)

Mechanisms of Action: HIPK2 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Shanghai YingLi Pharmaceutical
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for RLA-23174

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CTR20241636

P1

Unknown

Healthy Volunteers

None

Recent News Events

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Type

Title