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Hopital Beaujon

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France 100 Boulevard Du General Leclerc, 92110 Clichy, France

  • 81 trials recruiting
  • Hepatocellular carcinoma · Metabolic dysfunction-associated steatohepatitis · Hepatitis D
  • Adults and children

About Specializations

Hopital Beaujon in Clichy, France specialises in clinical trials of conditions such as Hepatocellular carcinoma, Metabolic dysfunction-associated steatohepatitis, Hepatitis D, Crohn's disease, and other specialisations. This site conducts important research.

Main research areas of the site

Liver Cancer Research

At Hopital Beaujon, investigators are evaluating new systemic and locoregional therapies for hepatocellular carcinoma, aiming to improve survival and disease control.

  • Immune checkpoint inhibitor combinations
  • Radioembolization with TheraSphere
  • Targeted agents such as livmoniplimab and budigalimab
  • Transarterial chemoembolization enhancements
  • Biomarker-driven treatment strategies

With over 100 active trials and more than 460 investigators, the site focuses on translating innovative treatments into clinical benefit for liver cancer patients.

Biliary Tract Cancer Studies

The department conducts studies on biliary tract cancers, including cholangiocarcinoma, to identify effective first‑line regimens and personalized approaches.

  • Combination chemotherapy versus immunotherapy
  • FGFR‑targeted agents for FGFR‑altered tumors
  • IDH1‑mutant disease-specific trials
  • Novel antibody‑drug conjugates
  • Surgical adjuncts and peri‑operative strategies

Research integrates molecular profiling to match patients with targeted therapies, reflecting the site’s commitment to precision oncology.

Metabolic Liver Disease (NASH/MASH)

Clinical programs address non‑alcoholic steatohepatitis and related metabolic dysfunction, testing agents that aim to resolve inflammation and fibrosis.

  • Oral farnesoid X receptor agonists
  • Fibrosis regression endpoints
  • Biopsy‑confirmed cirrhosis cohorts
  • Combination with lifestyle interventions
  • Long‑term safety monitoring

These trials seek to halt disease progression and prevent transition to cirrhosis, supporting a growing need for effective NASH therapies.

IgG4‑Related Disease Research

Investigators evaluate novel immunomodulators for IgG4‑related disease, targeting disease flares and steroid‑sparing outcomes.

  • Anti‑CD40 antibodies
  • B‑cell depletion strategies
  • Biomarker‑guided dosing
  • Quality‑of‑life assessments
  • Safety in multi‑organ involvement

The focus on IgG4‑RD reflects the site’s broader interest in immune‑mediated hepatic and systemic conditions.

Short Bowel Syndrome (SBS) Program

A dedicated program investigates therapies for short bowel syndrome and intestinal failure, aiming to reduce dependence on parenteral nutrition.

  • GLP‑2 analogues
  • Nutrient absorption enhancement
  • Long‑term safety in chronic use
  • Patient‑reported outcome measures
  • Combination with intestinal rehabilitation

These studies provide hope for improved nutrition and quality of life in patients with severe malabsorption.

Viral Hepatitis and Co‑Infection Trials

The site runs trials on chronic hepatitis B, hepatitis D, and HIV co‑infection, assessing antiviral combinations and functional cure strategies.

  • RNAi therapeutics
  • Novel capsid inhibitors
  • Combination with immune modulators
  • Biomarker‑driven treatment cessation
  • Safety in co‑infected populations

Efforts aim to achieve sustained viral suppression and reduce liver disease progression in high‑risk groups.

Inflammatory Bowel Disease Advances

Research includes advanced therapies for Crohn’s disease and ulcerative colitis, focusing on maintenance of remission and postoperative outcomes.

  • Selective IL‑23 inhibition
  • Therapeutic drug monitoring strategies
  • Post‑surgical recurrence prevention
  • Microbiome‑based interventions
  • Patient‑centred efficacy endpoints

Trials integrate endoscopic and clinical scores to optimize long‑term disease control.

Neuroendocrine Tumor (NET) Research

Studies target gastro‑enteropancreatic neuroendocrine tumors, evaluating peptide receptor radionuclide therapy and emerging systemic agents.

  • 177Lu‑edotreotide PRRT
  • SSTR‑targeted radioisotopes
  • Combination with checkpoint inhibitors
  • Biomarker‑guided patient selection
  • Quality‑of‑life outcomes

The program seeks to extend survival and improve symptom management for patients with metastatic NETs.

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Site location
100 Boulevard Du General Leclerc92110 ClichyFrance
Recruiting now
81 trials
Conditions studied
93
Partner status
Verified site

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Ongoing trials

Clinical trials currently enrolling participants at this site.

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182 clinical trials

Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Golimumab
  • Sponsor:Janssen Cilag International

A Phase III Study of Survodutide in Adults with Compensated NASH Cirrhosis to Assess Liver Outcomes and Safety

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:BI 456906
  • Sponsor:Boehringer Ingelheim International GmbH

A Phase III trial of BI 456906 weekly injections in adults with NASH and stage 2‑3 liver fibrosis

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:BI 456906
  • Sponsor:Boehringer Ingelheim International GmbH

A study testing XmAb942 compared to placebo in adults with moderate-to-severe active ulcerative colitis

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:XMAB942
  • Sponsor:Xencor Inc.

A study comparing XL092 versus everolimus in patients with previously treated advanced or metastatic neuroendocrine tumors

Registered drugNo placebo
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Everolimus
  • Sponsor:Exelixis Inc.

Study of Lutetium-177-DOTA-TATE with octreotide LAR in newly diagnosed patients with advanced gastroenteropancreatic neuroendocrine tumors (GEP-NET) with high disease burden

Registered drugNo placebo
Countries:FranceFrance
  • Participants:0–17 years · 18–64 years · 65+ years
  • Substances:Dimeticone
  • Sponsor:Novartis Pharma AG

Crohn's disease

Recruiting

Study of tulisokibart compared to placebo in adults with moderate to severe Crohn's disease

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Tulisokibart
  • Sponsor:Merck Sharp & Dohme LLC

Study on the Effects of Pegozafermin for Patients with Nonalcoholic Steatohepatitis (NASH) and Fibrosis

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:BIO89-100
  • Sponsor:F. Hoffmann-La Roche AG

Study of Pegozafermin Treatment for Patients with Liver Cirrhosis due to Metabolic Dysfunction-Associated Steatohepatitis (MASH)

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:BIO89-100
  • Sponsor:F. Hoffmann-La Roche AG

Study of Elafibranor for Adults with Primary Biliary Cholangitis

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Elafibranor
  • Sponsor:Ipsen Bioscience Inc.

Hepatic fibrosis+2

Recruiting

Study on Efruxifermin for Patients with Non-Cirrhotic Nonalcoholic Steatohepatitis (NASH) and Fibrosis

Investigational
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Efruxifermin
  • Sponsor:Akero Therapeutics Inc.

Study on the Long-term Safety and Efficacy of Pembrolizumab and Lenvatinib for Patients with Advanced Tumors

Registered drugNo placebo
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Favezelimab
  • Sponsor:Merck Sharp & Dohme LLC
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