News Blog

Wednesday, 10 May 2023 10:02

Expert advocates more clinical trials in Africa

Rate this item
(0 votes)

Expert advocates more clinical trials in Africa

A multinational biotechnology healthcare company, Roche, has lamented the low inclusion of Africa in global pharma studies, revealing that only 2.4 per cent of patients from the continent are enrolled in annual global clinical trials.

According to the company, African patients make up only about two per cent of genomic data for clinical trials despite the fact that the continent deals with more than 24 per cent of global disease burden.

These statistical facts were made known in a technical presentation which explained why the company launched the pilot Roche Advancing Inclusive Research Africa Site Alliance Project in Africa.

The Medical Director, Roche Products Nigeria Limited, Dr. Bola Oyedeji, while speaking at the launch of the project recently, said, “Only 2.4 per cent of clinical trials in the world are conducted in Africa and only two per cent of global genetic data is from Africa clinical trials out of the eight billion world population.”

He said the mission of Roche was to deliver three to five times more benefits to patients at half the cost to society, noting that the project would help in closing the data gaps and improving health in the long-term for all Nigerians and Africans.

“The vision of the Roche Advancing Inclusive Research Africa Site Alliance project is to create a site network in Africa to enable recruitment and retention of underrepresented patient populations to enrich science and enable the delivery of innovation so we can eliminate disparity in outcomes for all patients.

Source: HealthWise

Read 300 times

Information

NIROPHARM is dedicated to working to improve and enhance the quality of service to the Nation, public (local and international) Image, and the scope of the Nigerian Pharmaceutical Industry who face a number of challenges. 

Some of the challenges that NIROPHRM is set  to tackle with all the resources it has at its disposal include: High cost of funds, Poor infrastructure, Poor IPR protection, Chaotic drug distribution, Lack of data for planning, High level of Counterfeiting, Low capacity of Regulatory Agencies, Regulatory Agency, not computerized, Poor surveillance particularly at the land borders