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NCT07650773Recruiting

CHARM Hepatocellular Carcinoma MEA Study

A Multicountry, Multicenter, Secondary Data Collection, Retrospective Observational Study to Describe the Characteristics and Management of Hepatocellular Carcinoma (HCC) Among Adults in the Middle East Region

Source: ClinicalTrials.gov · Last updated 14 Oct 2026

Brief summary (registry, in English)

Hepatocellular carcinoma (HCC) is the sixth most commonly diagnosed cancer and the third reason for cancer-related death worldwide. Cirrhosis is a common risk factor of HCC, as it is found in approximately 70-90% of patients with HCC. Hepatitis C (HCV) and alcohol consumption represent the main causes of cirrhosis and HCC in Western countries; however, hepatitis B virus (HBV) is the leading cause of HCC and cirrhosis in East Asia and Africa. Moreover, HBV and HCV are considered the most common causes of HCC in about 80%-90% of patients. In addition, steatotic liver disease (SLD) is considered one of the main causes of HCC and cirrhosis. Unfortunately, the burden of HCC is great in Middle Eastern and North African (MENA) countries because of the high prevalence of HCV and HBV and the increasing incidence of SLD and metabolic-associated steatohepatitis (MASH). Several studies illustrated that there are great disparities in the survival rate of patients with HCC according to patient characteristics such as gender, age, and socioeconomic status. In addition, the etiology of HCC may impact the survival and the response to treatment. Moreover, the incidence of HCC could be decreased by the prevention and/or appropriate management of HCC risk factors, especially HBV, HCV infections, and SLD. Therefore, understanding the etiology, patient characteristics, pathogenesis, and optimal management of HCC in the region is considered of prime importance to improve the patient journey of HCC in the MENA region. The Middle East encompasses countries with varying levels of healthcare development and resources. There is a significant disparity in access to diagnostic tools, therapeutic options, and liver transplantation services. While some countries possess advanced healthcare systems with state-of-the-art facilities, others face challenges such as limited healthcare infrastructure, shortage of specialized healthcare professionals, and inadequate screening programs. These disparities significantly affect the early detection, management, and outcomes of HCC patients. This study aims to assess the etiology, clinical and tumor characteristics, and treatments received for HCC, as well as clinical outcomes (OS, PFS) in different countries in the MENA region.

Status (registry)
Recruiting
Study type
Observational
Enrollment
4000 (estimated)
First submitted
11 Jun 2026
Start date
Jul 2026
Primary completion date
Nov 2027
Lead sponsor
AstraZeneca
NCT number
NCT07650773

What you commit to

  • Study type: Observational
  • Planned participants: 4000
  • From Jul 2026 to the primary completion date, Nov 2027
  • 17 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously opted out of sharing medical records

Other illness

  • Patients with other cancer diagnosis on or before index date.

Lab values

  • Patients with records missing information on etiology, laboratory results, radiological findings, or treatment details (≥30% of key variables).

Other

  • Patients participating in clinical trials
  • Pregnant patient

Who the study is looking for

  • Patients with a radiological or histopathological confirmed diagnosis with HCC in any stage of the tumor between 1st January 2015 and 31st December 2023 (defined as index date).
  • Patient or next of kin/legal representative (for deceased patients at study entry, unless a waiver is granted) willing and able to provide written informed consent according to the local regulations
  • Age 18 years or older, and a lawful adult in the country at the index date
  • Patients with medical records, including etiology, laboratories, radiological, and treatment details will be collected from the participating sites.
  • Patients with medical records covering at least a 6-month follow-up period, defined as the time from the index date (the date of the first diagnosis) to the earliest of the following: the patient's death, the last medical record entry, or the data extraction date. Additionally, patients who died within this 6-month period will also be included.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Coordinator of this site? Confirm its status
Abu DhabiUnited Arab EmiratesNot yet recruiting
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Al Ain CityUnited Arab EmiratesRecruiting
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Al MansurahEgyptNot yet recruiting
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DakahliaEgyptNot yet recruiting
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DamiettaEgyptNot yet recruiting
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MenoufEgyptNot yet recruiting
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Kuwait CityKuwaitNot yet recruiting
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RabatMoroccoNot yet recruiting
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DohaQatarNot yet recruiting
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DammamSaudi ArabiaNot yet recruiting
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JeddahSaudi ArabiaNot yet recruiting
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MeccaSaudi ArabiaNot yet recruiting
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RiyadhSaudi ArabiaNot yet recruiting
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AnkaraTurkey (Türkiye)Not yet recruiting
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ErzurumTurkey (Türkiye)Not yet recruiting
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IstanbulTurkey (Türkiye)Not yet recruiting
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IzmirTurkey (Türkiye)Not yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.