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OPN-6602

Alternative Names: OPN-6602, OPN6602, OPN 6602
Latest Update: 2024-08-26
Latest Update Note: News Article

Product Description

OPN-6602 is a potent and selective EP300/CBP bromodomain inhibitor. OPN-6602 blocks signaling involved in cell growth and tumorigenesis by modulation of histone acetylation and the recruitment of EP300/CBP bromodomains. OPN-6602 reduces androgen receptor (AR)-driven and MYC gene expression while acting through a distinct mechanism from BET bromodomain inhibitors. Inhibition of AR signaling with OPN-6602 has been shown to reduce tumor growth in metastatic castration resistant prostate cancer (mCRPC) xenograft and PDX models. (Sourced from: https://www.opnabio.com/programs/opn-6602/)

Mechanisms of Action: p300/CBP 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: Opna Bio
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for OPN-6602

Countries in Clinic: United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Multiple Myeloma

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

OPN6602-C01

P1

Recruiting

Multiple Myeloma

2026-07-01

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