We have a very strong background in phase I studies, both in the hospital setting and in phase I volunteer units. We are able to advise on the relative merits of individual Phase I units throughout the UK, having worked regularly with most of them over the last ten years.
We have a wealth of experience in oncology with solid tumours, including breast, colorectal, head and neck and ovarian cancers, melanoma and other rare tumours such as glioblastoma. We have also worked in most haematological malignancies.
Our work in the cardiology and cardiovascular therapy areas includes studies on stents, artificial valve replacements, hypotension, hypertension, cardiomyopathy, ischemic heart disease, angina and exercise studies. These studies have involved numerous different therapy types, from aspirin and diuretics to beta-blockers, ACE inhibitors and calcium antagonists to lipid lowering agents.
We have many years of experience in working with infertility, women’s health, and endocrinology particularly with various female and male infertility conditions including studies in IVF. We have worked with hGH in the IVF setting (and in the traditional non-infertility setting) and other rarer conditions such as isolated hypogonadotrophic hypogonadism (IHH).
Dermatology is another strong area of expertise for CDSS. We have worked on psoriasis studies and numerous other skin conditions including wound healing and anti-scarring compounds.
We have worked with a wide variety of pain management drugs including totally new compounds through to those used in the oncology setting, particularly in pain associated with metastases secondary to prostate or breast cancer. These studies include both pharmaceutical and radiological studies.
This is just a selection of our experience, so if you don’t see your therapeutic area of interest described here, please give us a call to find out more as our portfolio is larger than we are able to describe here.
At CDSS we have worked with many different pharmaceutical, medical device and biotech companies, both large and small, in all of the above mentioned therapeutic areas. In all cases, we are able to project manage studies, monitor and if necessary, hold the Trial Master File within our head office in Cheshire, in the UK.