Welcome to Xcene Research, Africa’s leading Contract Research Organization (CRO) dedicated to advancing medical knowledge through innovative clinical research solutions. We take pride in fostering strong partnerships with sponsors to drive groundbreaking discoveries and accelerate the development of life-changing therapies for patients across the continent. Our commitment to excellence, scientific expertise, and unwavering ethics makes us the ideal collaborator for your clinical research endeavours.
Why Choose Xcene Research?
1. Extensive Expertise: With years of experience in the industry, our team of professionals brings a wealth of knowledge and expertise in managing clinical trials across Sub-Saharan Africa. We have successfully conducted numerous trials in diverse therapeutic areas, ensuring quality outcomes and regulatory compliance.
2. Local Advantage: As an African CRO, we possess a deep understanding of the local healthcare landscape, cultural nuances, and regulatory requirements. Our strong connections with local investigators, sites, and regulatory authorities enable us to navigate the unique challenges of conducting trials in Sub-Saharan Africa.
3. Quality and Compliance: At Xcene Research, quality is our top priority. We adhere to strict quality assurance protocols, ensuring that every aspect of the clinical trial meets the highest industry standards and regulatory guidelines. We employ robust quality control measures to guarantee data integrity, patient safety, and ethical conduct throughout the trial.
4. Tailored Solutions: We understand that each clinical trial is unique. Our flexible approach allows us to tailor our services to meet your specific needs and study requirements. Whether you require full-service support or specific functional areas, our dedicated team will work closely with you to develop a customized solution that aligns with your goals.
Success Story from Sponsor X
At Xcene Research, we have had the privilege of partnering with numerous sponsors from diverse industries and therapeutic areas. One such remarkable success story involves an anonymous sponsor who approached us with a Request for Proposal (RFP) for a groundbreaking sickle cell drug. Their goal was to conduct a multi-centre, double-blind, placebo-controlled Phase III clinical trial to assess the drug’s efficacy and safety in patients with sickle cell disease.
From the outset, our team of dedicated professionals collaborated closely with the sponsor to thoroughly understand their objectives and tailor a customized approach. Our deep knowledge of the African healthcare landscape and extensive investigator network allowed us to identify the most suitable research sites for the trial, ensuring robust patient recruitment.
The project’s success hinged on our meticulous project management, adherence to timelines, and rigorous data monitoring. Our site management team ensured seamless communication with investigators and provided them with the necessary training and resources. Meanwhile, our data management team meticulously processed and analyzed the trial data, delivering accurate and reliable results.
Through unwavering dedication and adherence to high-quality standards, we successfully completed the trial ahead of schedule, surpassing the sponsor’s expectations. The sickle cell drug showed remarkable promise, leading to its subsequent approval by regulatory authorities. This achievement not only brought hope to countless patients battling sickle cell disease but also opened doors for further collaborations with the sponsor on future research initiatives.
At Xcene Research, we believe that each partnership is a unique journey, and we are committed to creating success stories like this, one study at a time.
How to Become a partner
To begin our partnership journey, we invite you to submit an RFP. The RFP process allows us to better understand your study objectives, timelines, and specific requirements.
Once we receive it, our team of experts will thoroughly review the information and prepare a comprehensive proposal tailored to your study requirements. We may contact you for additional details or to schedule a discussion to better understand your needs.
