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Clinical Trials

Pioneering research. Early access to tomorrow's treatments. African cancer science, led from Africa.

Research Leadership

Africa Needs African Cancer Data

Historically, the world's most influential cancer trials have enrolled almost no African patients. Yet cancer biology, treatment responses, and disease patterns can differ significantly across populations.

Afri-German's Research Unit runs investigator-initiated and partnership trials specifically designed to generate evidence in our patient population -- closing the data gap and improving care for millions across the continent.

Our trials follow the strictest ethical and scientific standards, are reviewed by our Institutional Review Board, and are conducted in full compliance with ICH-GCP guidelines.

4
Active Trials
12
International Partners
340+
Trial Participants
100%
Ethics Compliant

Open to Enrolment

Current Clinical Trials

Phase IIRecruitingAGO-2024-001Cervical Cancer

SENTINEL-AFRI: Immunotherapy Plus Chemotherapy in Advanced Cervical Cancer

Evaluating the efficacy and safety of pembrolizumab combined with platinum-based chemotherapy as first-line treatment for advanced cervical cancer in Sub-Saharan African patients.

Sponsor: Afri-German Oncology in partnership with AORTIC

Key Eligibility Criteria:

Stage III-IV cervical cancerPreviously untreatedAge 18-65Adequate organ functionConfirmed HPV-positive histology
Phase II / IIIRecruitingAGO-2024-002Breast Cancer

PRECISE-NG: Genomic-Guided Therapy in Breast Cancer - A Nigerian Cohort Study

Investigating genomic profiling to guide personalised treatment selection in Nigerian breast cancer patients, comparing standard chemotherapy vs. genomically-matched targeted therapy.

Sponsor: Afri-German Oncology / German Cancer Aid Partnership

Key Eligibility Criteria:

Stage II-III HER2+ breast cancerFemale, age 25-70No prior systemic therapyAccessible primary tumourFit for standard chemotherapy
Phase IIIActive, Not RecruitingAGO-2024-003Liver Cancer

HEPATO-RESOLVE: Sorafenib vs. Lenvatinib in HBV-Associated Hepatocellular Carcinoma

A randomised controlled trial comparing two targeted therapy agents in HBV-associated liver cancer, with a sub-Saharan African patient population that has historically been underrepresented in global HCC trials.

Sponsor: Afri-German Oncology / WHO Africa Regional Oncology Network

Key Eligibility Criteria:

Hepatocellular carcinoma, unresectableHepatitis B-associatedChild-Pugh A liver functionNo prior systemic therapyAge 18+
Phase IIRecruitingAGO-2024-004All Cancer Types

MIND-CANCER-GH: Mindfulness-Based Intervention and Quality of Life in Cancer Patients

Evaluating the impact of an adapted Mindfulness-Based Cancer Recovery programme on quality of life, anxiety, and treatment adherence in Nigerian cancer patients.

Sponsor: Afri-German Oncology / King's College London Global Health Partnership

Key Eligibility Criteria:

Any cancer diagnosis, any stageCurrently receiving or recently completed treatmentAge 18+Able to attend weekly sessionsNo major psychiatric comorbidity

Why Participate in a Clinical Trial?

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Access Cutting-Edge Treatments

Clinical trial participants often access novel therapies not yet commercially available.

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Enhanced Medical Monitoring

Trial participants receive more frequent monitoring and closer medical attention than standard care.

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Advance African Oncology

Your participation generates vital data about cancer in African patients, improving care for future generations.

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Reduced or Zero Cost

Trial drugs and protocol-related tests are typically provided free of charge to participants.

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Expert Research Team

You are cared for by both your oncology team and our dedicated research nurses and coordinators.

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Withdraw Any Time

Participation is always voluntary. You may withdraw from a trial at any time without affecting your standard care.

How to Enrol

01

Express Interest

Contact our research team by phone or email to express interest in a specific trial.

02

Eligibility Screening

Our research coordinator reviews your medical records against trial eligibility criteria.

03

Informed Consent

A full explanation of the trial in your language so you can make a fully informed decision. No pressure.

04

Enrolment

Once you consent and are confirmed eligible, you are officially enrolled and treatment begins.

Our Ethics and Safety Commitments

All trials approved by our Institutional Review Board (IRB)
Full informed consent in your language, no pressure
Withdraw at any time without affecting standard care
Safety monitoring committees review data throughout
Any serious adverse events reported within 24 hours
Patient confidentiality protected under Nigerian data protection law (NDPR)

Contact Our Research Team

Have questions about a trial or want to check your eligibility? Our Research Coordinator is ready to help.