Ipsen

85 total trials 16 currently recruiting 50 completed

Ipsen sponsors 85 registered US clinical trials on ClinicalTrials.gov, 16 of them currently recruiting, and 50 completed. 33 of these trials are in Phase 3-4 (later-stage) and 28 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Primary Biliary Cholangitis, with 3 trials.

Trial Pipeline

85 total, page 2 of 2

COMPLETED Phase 2

Study of Nanoliposomal Irinotecan (Nal-IRI)-Containing Regimens Versus Nab-paclitaxel Plus Gemcitabine in Patients With Previously Untreated, Metastatic Pancreatic Adenocarcinoma

NCT02551991

COMPLETED

Validation Study of the SAGIT® Instrument in Acromegaly

NCT02539927

COMPLETED

Attainment of Person-centred Goals After Botulinum Toxin Treatment for Upper Limb Spasticity in Real Life Practice

NCT02454803

COMPLETED Phase 3

Efficacy And Safety Of Dysport In The Treatment Of Upper Limb Spasticity In Children

NCT02106351

COMPLETED Phase 3

Long Term Safety And Effectiveness Of Dysport® In Adults With Cervical Dystonia

NCT01753336

COMPLETED

SAGIT for Classification of Patients With Acromegaly in Clinical Practice

NCT02231593

COMPLETED Phase 3

Efficacy and Safety of DYSPORT® Using 2mL Dilution in Adults With Cervical Dystonia.

NCT01753310

COMPLETED

Phase IV-Cervical Dystonia-INTEREST IN CD2

NCT01753349

COMPLETED Phase 1

MM-398 (Nanoliposomal Irinotecan, Nal-IRI) to Determine Tumor Drug Levels and to Evaluate the Feasibility of Ferumoxytol Magnetic Resonance Imaging to Measure Tumor Associated Macrophages and to Predict Patient Response to Treatment

NCT01770353

COMPLETED Phase 3

Dysport® Adult Upper Limb Spasticity Extension Study

NCT01313312

COMPLETED Phase 3

Dysport® Pediatric Lower Limb Spasticity Follow-on Study

NCT01251380

COMPLETED Phase 3

Dysport® Adult Upper Limb Spasticity

NCT01313299

COMPLETED Phase 3

Dysport® Pediatric Lower Limb Spasticity Study

NCT01249417

COMPLETED Phase 3

Dysport® Adult Lower Limb Spasticity Follow-on Study

NCT01251367

COMPLETED

DYSPORT™ Clinical & Health Economics Outcomes Registry in Cervical Dystonia

NCT01314365

COMPLETED Phase 3

Dysport® Adult Lower Limb Spasticity Study

NCT01249404

TERMINATED Phase 2

Study of BN83495 in Post-menopausal Women With Endometrial Cancer Post-chemotherapy

NCT01251354

TERMINATED Phase 2

Study to Assess the Efficacy and Safety of Repeated Administration of BIM 23A760 in Patients With Acromegaly

NCT00994214

COMPLETED Phase 3

An Efficacy and Safety Study of Somatuline Depot (Lanreotide) Injection to Treat Carcinoid Syndrome

NCT00774930

COMPLETED Phase 3

Study of Lanreotide Autogel 120 mg in Patients With Non-functioning Entero- Pancreatic Endocrine Tumour

NCT00842348

COMPLETED Phase 1

BN83495 in Prostate Cancer

NCT00790374

COMPLETED

Somatuline® Depot (Lanreotide) for Acromegaly Post-Marketing Observational Study

NCT00686348

TERMINATED Phase 2

rhGH and rhIGF-1 Combination Therapy in Children With Short Stature Associated With IGF-1 Deficiency

NCT00572156

COMPLETED Phase 4

Safety/Efficacy of Tigan® to Control Nausea/Vomiting Experienced During Apokyn® Initiation and Treatment

NCT00489255

COMPLETED Phase 3

Assessment of the Ability of Subjects With Acromegaly or Their Partners to Administer Somatuline Autogel

NCT00447499

COMPLETED Phase 3

Study of Lanreotide Autogel in Non-functioning Entero-pancreatic Endocrine Tumours

NCT00353496

TERMINATED

IGFD Registry: A Patient Registry for Monitoring Long-term Safety and Efficacy of Increlex

NCT00747604

COMPLETED Phase 3

Open-label Extension Study of AbobotulinumtoxinA (Dysport®) for the Treatment of Cervical Dystonia

NCT00288509

COMPLETED Phase 3

Randomized, Placebo-Controlled Study of AbobotulinumtoxinA (Dysport®) for the Treatment of Cervical Dystonia

NCT00257660

COMPLETED Phase 2

Recombinant Human Insulin-Like Growth Factor (rhIGF-1) Treatment of Short Stature Associated With IGF-1 Deficiency

NCT00125190

TERMINATED Phase 3

Comparison of Lanreotide Autogel® and Sandostatin LAR Depot in the Treatment of Clinical Symptoms Associated With Carcinoid Syndrome

NCT00092287

COMPLETED Phase 3

Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency

NCT00125164

COMPLETED Phase 2

Study of a Single Administration of 3 Doses of Dysport® for the Treatment of Benign Essential Blepharospasm

NCT00234507

COMPLETED Phase 2

Efficacy and Safety Study of Varying Doses of Lanreotide Autogel in Patients With Acromegaly

NCT00234572

COMPLETED Phase 2

Long-Term Treatment With rhIGF-1 in GHIS

NCT00571727

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What the Pipeline for Ipsen Shows

According to the ClinicalTrials.gov registry, Ipsen is linked to 85 US clinical trials across every stage of research activity. Of those, 16 studies are currently recruiting, about 19% of the sponsor's indexed portfolio, and 50 are already marked complete, representing roughly 59% of the total.

The phase mix for Ipsen reports 33 late-stage studies (Phase 3 and Phase 4 combined) and 28 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Ipsen is Primary Biliary Cholangitis with 3 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.