Drug intelligence / Profile preview

ZGN-839

Development stage
Discontinued
Lead developer
Larimar Therapeutics
Modality
Small Molecules
01

Overview

ZGN-839 is a liver-targeted small molecule inhibitor of methionine aminopeptidase 2 (MetAP2) developed by Zafgen for the treatment of nonalcoholic steatohepatitis (NASH) and abdominal obesity. MetAP2 inhibitors modulate cellular processes controlling metabolism by directing binding to stress mediators, thereby reducing lipid synthesis in the liver and promoting fat metabolism as an energy source. This mechanism aims to address underlying metabolic dysregulation in NASH without the systemic effects seen in earlier MetAP2 inhibitors like beloranib.[3]

02

Targets

METAP2 (Methionine aminopeptidase 2)

Beyond the preview

Go deeper on ZGN-839.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on ZGN-839.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call