Email:
global@GCP-ClinPlus.com
GCP ClinPlus successfully delivered comprehensive clinical research services that led to the groundbreaking approval of China's first stem cell therapy for acute Graft-versus-Host Disease (aGVHD). Through strategic management, regulatory expertise, and clinical excellence, our team accelerated the product's market launch by four months, positioning it just 14 days after the approval of the first similar therapy in the United States—a testament to China's synchronization with global innovative medicine development.
This innovative stem cell product targeted aGvHD primarily affecting the gastrointestinal tract in patients who had failed hormone therapy. With no domestic or international precedents for stem cell therapy for aGvHD when the project started, the project faced three critical challenges:
● No established approval pathway in China for this novel therapeutic class
● Complex environmental requirements for preparation, storage, and transportation
● Heightened safety standards for cell-based therapies
● Sponsor's implementation of an aggressive countdown plan
● Traditional clinical development approaches inadequate for meeting deadlines
● Extended sample collection cycles threatening project viability
● 106 dedicated professionals across multiple disciplines
● Over 11,000 cumulative working hours
● End-to-end support spanning basic research through clinical studies to commercialization
● Maintained continuous communication with China's Center for Drug Evaluation (CDE)
● Monitored domestic and international regulatory developments
● Accelerated approval processes through strategic regulatory engagement
● Developed and enhanced the "Product Quality Traceability Code" system
● Ensured complete product quality traceability to meet stringent regulatory requirements
● Established protocols for consistent quality across complex biological products
Efficient Execution:
● Seamless coordination between hospitals, investigators, and resources
● On-site presence with 24/7 issue resolution capabilities
● Integrated planning, execution, and control within a PDCA management framework
Agile Adaptation:
● Optimized Phase II and III clinical trial designs
● Significantly shortened trial cycles through innovative approaches
● Rapid response to emerging challenges
Authoritative Expertise:
● Engagement of industry-leading experts for technical support
● Statistical experts from elite institutions
● Clinical specialists from top-tier hospitals and research institutes
Professional Implementation:
● End-to-end project services ensuring timely completion
● Rigorous standards maintaining data integrity
● Strategic milestone planning to accelerate regulatory approvals
First-of-its-Kind Approval
This stem cell therapy became the first of its kind approved for market in China, with regulatory authorization coming just 14 days after similar approval in the United States.
Global Significance
The approval represents a milestone in stem cell therapy development both in China and internationally, demonstrating China's ability to match global progress in innovative drug development.
Regulatory Precedent
The successful approval process contributed valuable experience to China's National Medical Products Administration (NMPA) review capabilities, establishing pathways for subsequent stem cell therapy products.
Accelerated Timeline
Through strategic management and optimization of clinical processes, GCP ClinPlus delivered the project four months ahead of the original schedule.
Founded in 2003, GCP ClinPlus brings 22 years of experience to every project we undertake. With over 500 global clients served and more than 2,200 clinical projects supported, we have established ourselves as a trusted partner in clinical research across therapeutic areas.
As an international CRO aligned with ICH standards, GCP ClinPlus remains committed to advancing transformative research in stem cell therapies, immune cell therapies, gene therapies, and other cutting-edge treatments. Our demonstrated success in navigating complex regulatory environments while maintaining rigorous scientific standards positions us as the partner of choice for innovative biotech companies seeking to accelerate their path to market.
If you're looking to accelerate your clinical development through enhanced patient enrollment—typically 2-3 times faster than in Western countries at a fraction of the cost—we invite you to contact us for a free initial consultation.
Our China-based clinical trials offer significant advantages:
● Access to vast patient populations
● Streamlined recruitment processes
● Cost-effective study execution
● ICH-compliant quality standards
● Experienced local teams with global expertise
Contact:
Suling Zhang
VP of International Operations and Business Development
Email: suling.zhang@gcp-clinplus.com
Phone: +1 (609) 255-3581
Website: gcpclinplus.com
This case study demonstrates GCP ClinPlus's ability to overcome unprecedented challenges in bringing novel cell therapies to market. Our comprehensive approach combines regulatory expertise, quality management excellence, and efficient project execution to achieve breakthrough results for clients in the advanced therapy medicinal product space.