Science-Driven. Patient-Centered.

Operating across 12 global research centers, Zenth Pharma invests over $4.2B annually in biomedical research, maintaining a pipeline of 80+ novel therapeutics and 18 approved molecular entities.

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Oncology

Next-generation targeted therapies, CAR-T cell engineering, and tumor microenvironment modulators for solid and hematologic malignancies.

Immunotherapy Targeted Small Molecules Cell Therapy
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Rare Diseases

Orphan drug development focused on orphan genetic disorders, lysosomal storage diseases, and metabolic deficiencies with high unmet medical need.

Gene Therapy Enzyme Replacement Antisense Oligos
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Neurology

Blood-brain barrier penetrating platforms, neuroinflammation modulators, and disease-modifying therapies for Alzheimer's, Parkinson's, and ALS.

Disease Modifying Neuroprotection Precision Diagnostics
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Immunology & Autoimmunity

Selective cytokine inhibitors, biologics for chronic inflammatory conditions, and microbiome-targeted immunomodulators.

Biologics Cytokine Blockade Microbiome
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Infectious Diseases

Broad-spectrum antivirals, novel antibiotic classes targeting resistant pathogens, and rapid-deployment vaccine platforms.

Antimicrobials Viral Enzyme Inhibitors Pandemic Response
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AI & Computational Discovery

Proprietary deep learning models for protein folding, target identification, and de novo molecular design reducing discovery timelines by 60%.

Generative Chemistry In Silico Trials Multi-Omics

Clinical & Preclinical Programs

Tracking our advanced molecular entities from discovery through FDA/EMA approval pathways.

Approved (18)
Phase III (9)
Phase II (14)
Phase I / Preclinical (39)
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Program Code Therapeutic Area Mechanism Approval Regions Status
ZP-401 Oncology (SCLC) PARP/ATR Dual Inhibitor US, EU, JP Approved 2024
ZP-512 Rare Disease (Pompe) Gene Augmentation (AAV) US, EU Approved 2023
ZP-608 Immunology (RA) Selective JAK3 Inhibitor Global Approved 2022
Program Code Indication Mechanism Partners Status
ZP-729 Metastatic Pancreatic CA Next-Gen CAR-NK NCT05881203 Phase III
ZP-814 Early Alzheimer's Tau-Targeting mAb NCT05990112 Phase III
ZP-880 Chronic Hepatitis B RNAi + Therapeutic Vaccine NCT06102244 Phase III
Program CodeIndicationMechanismReadout ETAStatus
ZP-901SARSCoV-2 Variant ShieldPan-Spike Nanobody CocktailQ4 2025Phase II
ZP-915Multiple SclerosisBBB-Permeable S1P ModulatorQ2 2026Phase II
Program CodeTargetModalityDiscovery LeadStatus
ZP-1042KRAS G12C/DCovalent Small MoleculeComputational AI PlatformPhase I
ZP-1088IL-23/IL-17 AxisBispecific AntibodyCambridge Biologics CenterPhase I

Centers of Excellence

Purpose-built laboratories, GMP manufacturing suites, and clinical trial coordination hubs across four continents.

📍 Cambridge, MA, USA
Headquarters & Discovery Hub
Target validation, AI-driven molecular design, translational medicine, and early-phase clinical operations.
📍 Basel, Switzerland
European Biologics Center
Antibody engineering, cell therapy manufacturing, and EMA regulatory strategy coordination.
📍 Singapore
APAC Manufacturing & Supply Chain
cGMP production for biologics, viral vector scaling, and regional distribution logistics.
📍 Tokyo, Japan
Advanced Therapies & Rare Disease
Gene therapy vector optimization, orphan drug clinical trials, and PMDA regulatory submissions.
📍 San Diego, CA, USA
Computational & Systems Biology
Multi-omics integration, digital twin modeling, and high-throughput screening automation.
📍 Oxford, UK
Academic & Innovation Partnerships
University co-development programs, licensing pipeline, and early-stage biotech incubation.

Regulatory & Ethical Standards

Every program adheres to rigorous international standards, ensuring patient safety, data integrity, and transparent development.

FDA / EMA / PMDA Aligned

All trials follow ICH-GCP guidelines with continuous regulatory agency feedback integration.

cGMP Manufacturing

WHO-certified facilities operating under strict quality control, batch release protocols, and audit readiness.

Ethical AI Governance

Transparent algorithmic auditing, bias mitigation frameworks, and human-in-the-loop validation for computational discovery.

Data Integrity & Privacy

HIPAA/GDPR-compliant clinical data management with end-to-end encryption and decentralized trial platforms.

Collaborate with Zenth Pharma

Explore co-development partnerships, investigator-initiated trials, or clinical site opportunities.

Partnership Inquiries → Join Our Research Teams