Oncology Clinical Trials

Oncology Clinical Trials Experts

Obatica oncology has supported many Oncology clinical trial
studies, many are early phase. Our Oncology specialist are fully qualified and
licensed consultant Oncologist, with patient care, and Principal Investigator as
well as industry experience in the drug development ecosystem.

As the field of Oncology advances, it is becoming more imperative
that Oncology clinical trial study has the guidance from a highly experience oncology
specialist.

The delicate balance cancer patient care, knowledge of the
current cancer drug development landscape, and adverse event/safety management
will enhance the success rate of your drug going to the next phase.

How Obatica Oncology Support Oncology Clinical Trials

Obatica supports Oncology focused biotech throughout the life cycle of your candidate.

1. Oncology Drug Development Clinical Strategy

Obatica often reviews a drug candidate’s pre-clinical study result including animal, toxicology report. Then together with the sponsor’s scientist and expert, Obatica will present, discuss and formulate the optimal clinical strategy in the format of study synopsis or ethics’s ready Investigator’s Brochure, or  Clinical Study Protocol. Study synopsis is often required to obtain quotes from different service providers.

Obatica can also support in the creation of clinical strategy presentation for the purpose of investor reach.

2. Oncology Clinical Trial Medical Writing

Oba

“Obatica is one of the best medical writers that we have worked with.  We were impressed not only by the high quality of their work but also their ability to deliver the protocols under very ambitious timelines, customer-orientated attitude and overall value.  We look forward to working with Obatica again on our future medical writing projects.” 

Kon Yew Kwek, BMBCh, DPhil.  Chief Medical Officer, Hummingbird Bioscience