Overview & Mission

The Zenth Clinical Research Network (ZCRN) operates a globally integrated infrastructure for clinical investigation, spanning 142 accredited sites across 38 countries. Our multidisciplinary teams leverage adaptive trial designs, decentralized methodologies, and AI-driven patient matching to accelerate therapeutic discovery while maintaining uncompromising ethical standards.

From early-phase pharmacokinetic studies to large-scale Phase IV post-market surveillance, ZCRN bridges the gap between laboratory innovation and clinical application, ensuring regulatory excellence and measurable patient impact.

Active Clinical Pipeline

ZCRN-ONC-2024-089 Phase III Oncology Immunotherapy

Efficacy of AZ-4021 in Advanced Non-Small Cell Lung Cancer

Randomized, double-blind, placebo-controlled multicenter study evaluating survival outcomes and immune response markers in NSCLC patients.

Multi-regional Biomarker-stratified Adaptive Design
842 / 1,200Enrolled
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ZCRN-NEU-2025-114 Phase II Neurology Gene Therapy

AAV-Mediated Delivery for Early-Stage Alzheimer's Disease

Dose-escalation study assessing neurocognitive preservation and amyloid-beta clearance via intrathecal vector administration.

De-centralized Digital Endpoints
215 / 350Enrolled
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ZCRN-RAR-2025-037 Phase IV Rare Diseases Longitudinal

Post-Market Safety Profile of Zentharaβ„’ in Spinal Muscular Atrophy

Real-world evidence collection tracking long-term tolerability, functional outcomes, and caregiver quality-of-life metrics across pediatric cohorts.

Real-World Data Patient-Reported Outcomes
1,150 / 1,150Enrolled
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Research Focus Areas

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Oncology & Hematology
47 Active Trials
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Neurodegenerative Disorders
31 Active Trials
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Cardiovascular & Metabolic
28 Active Trials
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Infectious Disease & Immunology
22 Active Trials
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Rare & Orphan Diseases
18 Active Trials
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Digital Health & AI Diagnostics
14 Active Trials

Compliance, Ethics & Data Integrity

All ZCRN operations adhere to international regulatory frameworks and institutional review board (IRB) oversight. We maintain full transparency through decentralized audit trails and blockchain-verified data logging.

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Regulatory Alignment
FDA 21 CFR Part 11, EMA GCP, PMDA, NMPA & Health Canada
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Ethics & IRB
Central & site-specific IRB/IEC approval for all protocols
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Data Privacy
HIPAA, GDPR & cross-border data transfer compliant
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Audit Readiness
24/7 remote monitoring & immutable eSource documentation

Access Portals

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Patient & Participant
Search active trials, check eligibility, and enroll securely.
Find Trials
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Researcher & PI
Protocol submission, site activation, and data dashboards.
Researcher Login
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Pharma & Biotech Partners
CRO services, site sourcing, and alliance management.
Partner Portal