OTD is a CRO focused on oncology, specialised in the anticancer drugs.

OTD is a small and flexible team – our team is composed of MD, PhD or MSc) with a collective experience managing over 60 Phase I-II oncology clinical trials, and fully committed to quality and transparency.

The client benefit is to fully achieve the objectives and in the fastest possible time.

We provide the following services:

• Protocol Writing & e-CRF Design
• Regulatory Applications
• Project Management
• PV
• Monitoring
• Data Management (preferred vendor)
• Report and Publications writing

OTD unique approach:

• Our Tactics: OTD’s medical oncologists closely review every patient “hands-on and in real-time”, while there is still time to address eligibility, toxicity and dosing issues.
• Special resources: Access to leading Principal Investigators and unique patient populations worldwide.

We have a specificity our experience in Phase I First-in Man managing clinically relevant information, analysis and transfer to Sponsor.

Tumour types and therapies

Solid tumours: Bladder, breast, cholangiocarcinoma, colorectal, glioblastoma, head & neck, hepatoma, lung, melanoma, ovary, pancreatic, prostate, renal, sarcomas, stomach, thyroid, and rare tumour types (eg, NMC)

Hematologic malignancies: leukaemia (ALL, AML), Hodgkin’s and non-Hodgkin’s lymphomas, β-hemoglobinopathies (SCA and β-thalassemia major), myeloproliferative disorders

Monotherapy / Combinations: classic cytotoxics, targeted therapeutic agents (small molecules and monoclonal antibodies), hormonal therapies, cell-based therapies, vaccines.

For more information on what OTD can offer you, please fill out the enquiry form attached to this page.