Ozmosi | BEBT-730 Drug Profile
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BEBT-730

Alternative Names: BEBT-730, BEBT730, BEBT 730
Clinical Status: Active
Latest Update: 2026-02-05
Latest Update Note: Clinical Trial Update

Product Description

BEBT‑730 — URAT1 | Hyperuricemia & Gout: In 293T‑hURAT1 cells, 10 nM achieved 93% URAT1 mRNA reduction. In a mouse hyperuricemia model, a single 5 mg/kg dose normalized serum urate, comparable to daily benzbromarone. A 4-week mouse tox study (200 mg/kg ×3) showed no clinical or clinical‑chemistry liabilities; next steps include NHP PK/PD, GLP tox, and CMC for IND. (Sourced from: http://www.bebettermed.com/#pipeline)

Mechanisms of Action: URAT1 Inhibitor

Novel Mechanism: No

Modality: Nucleic Acid

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: BeBetter Med
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

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Phase 0: Gout

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