Highlights
T-TOP was funded in January 2015. We provide full professional services in our areas of expertise, including clinical research and clinical trial conduct while maintaining compliance with ICH GCP guidelines. Our management team has extensive clinical trial management experience in global CROs & pharmaceutical companies. In addition, T-TOP has a comprehensive training program to ensure that T-TOP staffs are well equipped to provide exemplary services. These elements combine to allow T-TOP to maintain a smooth working relationship with partner companies and ensure timely and precise delivery of our products. Lots of CSRs had been submitted to US FDA for BLA/PMA application.
T-TOP has the highest flexibility to collaborate with pharmaceutical/ biotech companies in different kinds of clinical trials. More than 300 Study Nurses in affiliated SMO fully support the site activities. Below are T-TOP-conducted clinical trials:
| Disease Area/ Indication |
Phase |
Subjects |
| IVD for CEA125 |
III |
500 |
| IVD for Alzheimer Disease |
III |
240 |
| Pneumonia |
III |
80 |
| Microbiota |
Pilot |
36 |
| NSCLC |
Pilot |
100 |
| Gene therapy |
I/II |
24 |
| PTCL |
III |
67 |
| Hepatitis C |
III |
50 |
| Atopic Dermatitis |
IIa |
12 |
| Allergic Asthma |
IIa |
12 |
| Vitiligo |
0 |
10 |
| Atopic Dermatitis |
IIa |
12 |
| Hepatitis C |
IIT |
40 |
| Enterovirus |
III |
1276 |
| Neuroimage |
0 |
36 |
Services
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Data Management & Statistics
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Study design consulting, Study documents writing
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Regulatory Submission (CTD format)
