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Recruiting Phase 1, Phase 2 NCT06527495

NCT06527495 Clinical Pharmacogenetic Study of Sorafenib in Egyptian Patients With Hepatocellular Carcinoma

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Clinical Trial Summary
NCT ID NCT06527495
Status Recruiting
Phase Phase 1, Phase 2
Sponsor Assiut University
Condition HCC
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2023-01-01
Primary Completion 2024-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Sorafenib

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 150 participants in total. It began in 2023-01-01 with a primary completion date of 2024-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The current study will aim to maximize the therapeutic effect and to minimize the adverse effects of sorafenib in HCC through pharmacogenomic analysis of VEGFA and KDR genetic polymorphisms.

Eligibility Criteria

Inclusion Criteria: * Age of all studied subjects ≥ 18 years old * All patients with hepatocellular carcinoma will be included in group I. * Patients not treated with systemic TKIs Exclusion Criteria: * Patients presented with liver tumors other than HCC. * Patients with Child-Pugh grade C for liver function. * Patients with other malignancies. * Patients with chronic inflammatory disorders. * Patients with severe organ dysfunction such as heart, lung, and kidney. * Patients who cannot tolerate or are allergic to sorafenib. * Patients with severe coagulation dysfunction were uncorrectable. * Age less than 18 years old.

Contact & Investigator

Central Contact

Mahmoud Nazih

✉ Mahmoud.Nazih5698@pharm.aun.edu.eg

📞 00201093859868

Frequently Asked Questions

Who can join the NCT06527495 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying HCC. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06527495 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06527495 currently recruiting?

Yes, NCT06527495 is actively recruiting participants. Contact the research team at Mahmoud.Nazih5698@pharm.aun.edu.eg for enrollment information.

Where is the NCT06527495 trial being conducted?

This trial is being conducted at Shibīn al Kawm, Egypt.

Who is sponsoring the NCT06527495 clinical trial?

NCT06527495 is sponsored by Assiut University. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology