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IPSEN, OOO

🇫🇷France
Ownership
-
Established
1929-01-01
Employees
5.7K
Market Cap
$9.8B
Website
https://www.ipsen.com/

Clinical Trials

277

Active:8
Completed:197

Trial Phases

5 Phases

Phase 1:24
Phase 2:51
Phase 3:69
+2 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (166 trials with phase data)• Click on a phase to view related trials

Phase 3
69 (41.6%)
Phase 2
51 (30.7%)
Phase 1
24 (14.5%)
Phase 4
18 (10.8%)
Not Applicable
4 (2.4%)

A Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Anti-tumour Activity of IPN01203 in Adults With Locally Advanced or Metastatic Solid Tumours Exposed to Immune Checkpoint Inhibitor Therapies

Not Applicable
Not yet recruiting
Conditions
Advanced Solid Tumor
Metastatic Solid Tumor
Interventions
Biological: IPN01203
First Posted Date
2025-10-09
Last Posted Date
2025-10-09
Lead Sponsor
Ipsen
Target Recruit Count
102
Registration Number
NCT07213830

A Study to Assess the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic, Immunogenicity and Antitumour Activity of IPN60300 in Adults With Locally Advanced or Metastatic Solid Tumours

Not Applicable
Not yet recruiting
Conditions
Locally Advanced Solid Tumor
Metastatic Solid Tumor
Interventions
First Posted Date
2025-10-09
Last Posted Date
2025-10-09
Lead Sponsor
Ipsen
Target Recruit Count
102
Registration Number
NCT07213817

A Study to Assess the Genetic Variations in Bile Flow Disorders: Linking Progressive Familial Intrahepatic Cholestasis (PFIC)-Related Genes to Symptoms in Adults With Recurrent Cholestasis in Spain

Not yet recruiting
Conditions
PFIC - Progressive Familial Intrahepatic Cholestasis
First Posted Date
2025-09-25
Last Posted Date
2025-09-25
Lead Sponsor
Ipsen
Target Recruit Count
150
Registration Number
NCT07191704

A Study of the Effectiveness, Safety and the Long-term Outcomes of Participants With Progressive Familial Intrahepatic Cholestasis (PFIC) Who Take Odevixibat (Bylvay) in South Korea

Not yet recruiting
Conditions
Progressive Familial Intrahepatic Cholestasis
First Posted Date
2025-09-22
Last Posted Date
2025-09-22
Lead Sponsor
Ipsen
Target Recruit Count
10
Registration Number
NCT07185919

A Study Describing Scratch and Sleep Patterns in Patients With Primary Biliary Cholangitis (Luminaria)

Recruiting
Conditions
Primary Biliary Cholangitis
First Posted Date
2025-07-03
Last Posted Date
2025-10-01
Lead Sponsor
Ipsen
Target Recruit Count
30
Registration Number
NCT07049887
Locations
🇺🇸

Arizona Liver Center, Chandler, Arizona, United States

🇺🇸

University of Miami School of Medicine, Center for Liver Diseases, Miami, Florida, United States

🇺🇸

UT Southwestern Medical Center, Department of Internal Medicine, Digestive and Liver Diseases, Dallas, Texas, United States

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News

Ipsen's IPN10200 Shows Superior Long-Term Efficacy in Phase II Glabellar Lines Trial

Ipsen's internally developed IPN10200 demonstrated statistically significant improvement in glabellar lines at Week 4 versus placebo in the Phase II LANTIC trial.

Ipsen's Bylvay Receives Japanese Approval for Rare Liver Disease PFIC, Offering First Non-Surgical Treatment Option

Japan's Ministry of Health, Labour and Welfare has approved Bylvay (odevixibat) as the first once-daily ileal bile acid transport inhibitor for treating pruritus in progressive familial intrahepatic cholestasis patients.

Parabilis Medicines Appoints Fawzi Benzaghou as Chief Medical Officer to Advance "Undruggable" Cancer Targets

Parabilis Medicines has appointed Fawzi Benzaghou, M.D., as Chief Medical Officer to lead clinical and regulatory strategy for its pipeline targeting historically "undruggable" cancer proteins.

Merck KGaA Partners with Skyhawk Therapeutics in $2 Billion RNA Splicing Collaboration for Neurological Disorders

Merck KGaA, Darmstadt, Germany has entered a strategic collaboration with Skyhawk Therapeutics valued at over $2 billion to discover novel RNA-targeting small molecules for neurological disorders with high unmet medical need.

Day One Biopharmaceuticals Reports 310% Revenue Surge for Pediatric Cancer Drug OJEMDA

Day One Biopharmaceuticals reported OJEMDA net product revenue of $33.6 million in Q2 2025, representing a 310% year-over-year increase driven by expanding adoption among pediatric oncologists.

IRIC and Ipsen Initiate Phase 1 Trial of RAF Inhibitor IPN01195 for Solid Tumors

IRIC and IRICoR announced the start of a Phase 1 clinical trial for IPN01195, a RAF inhibitor small molecule therapy for solid tumors licensed to Ipsen in July 2025.

NAPOLI 3 Post-Hoc Analysis Identifies Characteristics Associated with Long-Term Survival in Metastatic Pancreatic Cancer

A post-hoc analysis of the Phase III NAPOLI 3 trial identified characteristics associated with long-term survival in metastatic pancreatic adenocarcinoma patients treated with the NALIRIFOX regimen.

World ADC San Diego Conference Highlights Growing Industry Focus on Antibody-Drug Conjugates

The 15th World ADC San Diego conference (November 4-7, 2024) represents the industry's largest and most comprehensive ADC-focused forum, featuring 120+ speakers across six development tracks.

Liver Cirrhosis Pipeline Shows Strong Growth with 30+ Therapies in Development Across Multiple Clinical Phases

DelveInsight's 2025 pipeline analysis reveals over 30 companies developing 30+ liver cirrhosis therapies, with promising candidates like Rezdiffra, efruxifermin, and belapectin showing significant clinical progress.

GENFIT Reports Strong 2024 Financial Results with First Commercial Revenues from Iqirvo®

GENFIT reported a net profit of €1.5 million for 2024, driven by €67.0 million in revenues including a €48.7 million milestone payment and royalties from Iqirvo® (elafibranor) sales in PBC.

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