local_hospital

Hôpital Estaing - CHU de Clermont-Ferrand

Address
1 Rue Lucie et Raymond Aubrac, 63003 Clermont-Ferrand, France

Hôpital Estaing - CHU de Clermont-Ferrand

Hôpital Estaing, part of the CHU de Clermont-Ferrand, is a leading academic medical center conducting advanced clinical research across multiple therapeutic areas. The center demonstrates particular expertise in oncology, hepatobiliary disorders, autoimmune conditions, and precision medicine approaches guided by genomic biomarkers.

  • Hepatobiliary diseases including primary biliary cholangitis with novel combination therapies
  • Oncology studies spanning primary CNS lymphoma, pancreatic ductal adenocarcinoma, colorectal cancer, and targeted therapies for BRAF-mutated tumors
  • Autoimmune and inflammatory conditions such as granulomatosis with polyangiitis
  • Immunotherapy combinations and precision medicine trials utilizing molecular profiling

The research center participates in innovative trials evaluating immunotherapy combinations including checkpoint inhibitors, targeted molecular therapies for specific genomic alterations, and salvage treatment strategies for patients with inadequate response to standard therapies. Their portfolio reflects a commitment to personalized medicine, focusing on biomarker-driven patient selection including HLA typing, microsatellite instability status, and BRAF mutation analysis to optimize treatment outcomes across diverse malignancies and complex autoimmune disorders.

Site Overview

assignment
6
connected trials
corporate_fare
4
sponsors
science
23
IMPs

Activity Indicator

Last 6 months

0
Trials started
0
Trials started 6–12 months ago
6
Total trials linked
Active
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Mar
Apr
May
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Trial Flow

How this site's trials are distributed across therapeutic areas and active substances (IMPs), and how they're positioned within their overall lifecycle status. Flow thickness represents the number of unique trials.

Therapeutic areaarrow_forwardIMParrow_forwardLifecycle status

Top 2 of 3 therapeutic areas and 15 of 23 IMPs, ranked by number of trials.

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Compounds & Molecules Timeline

The time span of clinical-trial activity for the main active substances (IMPs) studied at this site over the last 8 years. Each bar runs from the earliest trial start to the most recent end; a substance with a trial still open has no recorded end and is shown as ongoing.

Trial span Ongoing Showing last 8 years
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Sponsor & Partnership

Top sponsors by active trials, and the ones that have come back for more than one study.

Active trials
4
Sponsors (total)
4
Active sponsors
2

Sponsor Network

Top 2 by active trials.

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Partnership History

Sponsors with repeated collaboration (≥ 2 trials).

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Sponsor Network Graph

How sponsors and therapeutic areas connect across this site's active trials: each link is at least one active trial shared between them, and bigger nodes mean more activity. Click a node to see its exact connections.

Country Benchmark

Compared to 978 other sites in France

description
Trial volume
6
Outperforms 66% of sites
public
Therapeutic diversity
3areas
Outperforms 59% of sites
groups
Sponsor diversity
4sponsors
Outperforms 62% of sites

Therapeutic Area Benchmark — France

Select a therapeutic area to compare against other sites in France.

Competitor Comparison

Similar sites in the same country running a comparable number of trials (within ±30%), scored on how closely their trial portfolios match this one. Higher percentages mean a more similar profile.

Country: France

Market Share

Country: France

Therapeutic Area Market Share

Select a therapeutic area to view its disease coverage breakdown.

Heat Maps & Advanced Analytics

How often specific conditions appear in trials across this site and comparable sites from the same country. Each row is a site, each column a condition, and each cell the number of trials on it — darker means more activity.

Other Trials in Hôpital Estaing - CHU de Clermont-Ferrand

lock Showing 1 of 6 trials — the rest is available on a paid plan.

Trial Sponsor Phase Status Start Date End Date
Evaluation of Bezafibrate 400 mg and 200 mg as Adjunctive Therapy in Primary Biliary Cholangitis with Suboptimal Ursodeoxycholic Acid Response: A Randomized, Double-Blind, Placebo-Controlled TrialAssistance Publique Hopitaux De ParisPhase IIIRecruitingMar 2025

IMP list

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IMP Trials Status First start Last start
Azathioprine1Unknown2025-06-062025-06-06

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