Ozmosi | ALXN-2420 Drug Profile
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ALXN-2420

Alternative Names: ALXN-2420, ALXN 2420, ALXN2420
Clinical Status: Inactive
Latest Update: 2026-02-03
Latest Update Note: Clinical Trial Update

Product Description

A novel, small peptide antagonist of the growth hormone receptor (GHR), being developed as a combination therapy to SSAs to further suppress and normalize IGF1 levels. ALXN2420 bound to the human GHR and inhibited its activation by GH in vitro. In vivo, ALXN2420 administration efficiently reduced IGF1 levels, which was associated with reduced growth in juvenile rats. Importantly, when combined with a SSA, ALXN2420 demonstrated an additive effect on IGF1 reduction. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/40067863/)

Mechanisms of Action: GHR Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Subcutaneous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: AstraZeneca
Company Location: Europe
Company Founding Year: 1999
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for ALXN-2420

Countries in Clinic: Argentina, Brazil, China, Denmark, Hungary, Italy, Lithuania, Netherlands, Poland, Romania, United States

Active Clinical Trial Count: 2

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Acromegaly

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT07037420

ASTERIA

P2

Recruiting

Acromegaly

2027-01-08

50%

2026-02-04

Primary Endpoints

2025-521243-20-00

ALXN2420-Acro-201

P2

Not yet recruiting

Acromegaly

2027-12-31

Recent News Events

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