 With the clinical operations office in St. Petersburg (Russia) and the business administration group in San Francisco (USA), we have the skills and resources to conduct complex clinical research projects in major therapeutic areas and provide complete logistical support to your studies. CCCP offers to its clients: - Expedited start-to-completion study time
- Patient recruitment capabilities including access to naïve patients
- Competitive pricing
Broad clinical expertise combined with the extensive drug development experience of CCCP’s key personnel provide our clients with a unique opportunity to rapidly assess the applicability and efficacy of their therapeutic candidates. Our areas of expertise are: - Concept and implementation of Phase I/IIa proof of target and proof of concept clinical trials for molecular targeted therapies, including study design, clinical sample acquisition for correlative studies and for patient pre-selection criteria, and experimental analyses of patient samples post-treatment;
- Design and implementation of scientifically challenging clinical studies aimed at understanding the mechanism of action, efficacy, and drug resistance of therapeutic agents.
Vital relationships with key clinical sites, successful patient recruitment strategies and effective logistics solutions allow us to minimize potential delays in study timelines and maximize your research investments. |