Therapeutic Expertise

Cell and Gene Therapy

Support seamless execution of CGT clinical development.

Flexible End-To-End Engagement Models and Customized Approaches

In recent years, cell and gene therapy (CGT) has developed rapidly, raising the bar for research, manufacturing and clinical development. Tigermed’s team of experts in cell and gene therapy clinical trials covers a wide range of cell, gene and small nucleic acid products, including gene therapy, stem cells, CAR-T, CAR-NK, TCR-T, TIL and red blood cell therapies, across indications such as multiple myeloma, lymphoma, hemophilia, rare diseases and autoimmune diseases.

In terms of industry resources, Tigermed’s cell and gene therapy solutions have a team of top experts, 100+ KOL resources, more than 200 professional CGT strategic cooperation centers, as well as a number of cooperative GCP centers and scientific research institutions, integrating advantageous resources to serve CGT customers.

In addition, relying on the integrated R&D service platform for innovative drugs, Tigermed’s professional CGT solutions can provide integrated and specialized cell and gene therapy CRO services ranging from preclinical super-cell donor library screening services, CMC, pharmacodynamic modeling exploration, pharmacology and toxicology, GLP safety assessment center, registration, medicine, operation, numerical statistics, PV, MM, SMO, CGT special testing project center laboratory, etc., and provide customized services for R&D institutions according to their needs. We can also provide R&D institutions with customized cell and gene therapy consulting, including project strategy planning, and other professional services according to their needs, so as to accelerate the clinical development and marketing process of CGT products in an efficient and high-quality way.

CGT Clinical Development

Senior experts and dedicated teams focused on CGT solutions provide integrated cell and gene therapy development services, from preclinical super cell donor bank screening to pharmacodynamic and toxicological studies, registration filing and clinical trials, as well as consultative project formulation strategy planning and specific professional support for CGT therapeutic areas.

CGT clinical studies
170+
Stem cells clinical studies
50+
Gene therapy clinical studies
150+

Benefits for Your Cell and Gene Therapy Development Life Cycle

Providing customized and insightful study designs

New drug types / New mechanisms of action / Existence of faster-moving analogs...

Identifying product value, market access and positioning

Assessment of clinical value, market positioning and potential differentiation based on unique mechanisms of the drug type, characteristics of the target indications

Evaluating the possibility of exceeding study timelines

Formulate competitive and differentiated development strategies and assess the feasibility of accelerated approval, dual reporting in China and abroad, and international multi-center clinical designs

Estimating the risks of amendment and delays

Managing Complexity in Clinical Implementation /
Difficult Identification and Response /
Assessment of the likelihood of poor efficacy /
Assessment of Insufficient Evidence of Safety /
...

Improving your protocols with up-to-date market and regulatory intelligence

Adapt clinical development strategies and trial protocols according to the latest regulatory requirements and competitive developments

Cell and Gene Therapy Clinical Trials Delivered by Indications

Multiple Myeloma

Periodontitis

Leukaemia

Hepatocellular
Carcinoma

Lymphoma

Crohn's Disease

Hematologic Malignancies

Rare Disease

Solid Tumor

Sequela of Apoplexy

Parkinson’s Disease

NSCLC

COPD

ARDS

Hemophilia

Thalassemia

Coronary Heart Disease

Ulcerative Colitis

Autoimmune Disease

Pneumonia

Gastric Carcinoma

GVHD

Osteoarthritis

Ophthalmology

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