Company intelligence / Profile preview

N-Zyme Biomedical

United Statesnzymebio.com ↗
Ownership
Private
Development stage
Phase 3
01

Overview

N-Zyme Biomedical has developed a novel class of pepsin inhibitor therapies targeting LPR and GERD. Their lead program, NZYM-001, uses a repurposed HIV protease inhibitor formulated as an oral suspension and dry powder inhaler to locally inhibit pepsin activity. The company’s approach leverages existing safety data to accelerate clinical development. A Phase II proof-of-concept trial for their proprietary sustained-release oral fosamprenavir sodium alginate formulation will begin enrollment in Spring 2025. An IND has been approved by the FDA for a related study at the Medical College of Wisconsin using standard fosamprenavir/Lexiva.

Therapeutic areas
Gastroenterology
Modalities
Repurposed small molecule drugs (notably HIV protease inhibitors such as fosamprenavir)Oral suspension formulationsDry powder inhaler formulations
Industry
Biotech
02

Drug pipeline

1 asset

NZYM-002

Preclinical
03

Partnerships

LGM Pharma – CDMO partner supporting API sourcing, drug product manufacturing, and clinical supply chain management for new prolonged release formulations.Medical College of Wisconsin – Clinical research collaboration on IND-approved trials.

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