Ipsen

Open enrollment across a mixed-phase pipeline

According to ClinicalTrials.gov-derived indexes, Ipsen sits in the top decile of US sponsors by registered trial count (#268 of 15,742 sponsors by registered trial count).

85 total trials 16 currently recruiting 50 completed top decile by trial count

Ipsen: 85 sponsored US clinical trials, 16 recruiting.

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.

Top-decile sponsor footprint

Ipsen ranks in the top decile of sponsors by registered trial count (#268 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

F 41/100

50 of 62 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (80.6%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Open and recent trials

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 is open in the Ipsen pipeline

16 recruiting of 85 indexed (19% open); 50 completed (59%).

Phase mix: 33 late (III/IV) vs 28 early (I/II) (balanced across stages).

Top condition: Primary Biliary Cholangitis (3 trials), 9 others listed.

How open-pipeline share is computed

Recruiting share is recruiting_count divided by trial_count for this sponsor in the public registry export. Status can change between pulls; treat the figure as a research-attention snapshot, not product availability.

Ipsen: open-pipeline peers nationwide

Peers matched on 85 registered trials and 19% open enrollment, not the therapeutic-area sidebar.

Ipsen sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 0200400600800 0%5%10%15%20% Total trials Recruiting share IpsenIntermountain Health CareSeagenFerring PharmaceuticalsNational Jewish HealthSpaulding Rehabilitation HospitalMedical University of South CarolinaEyePoint PharmaceuticalsHebrew SeniorLife
Ipsen sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

Ipsen sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 85 trials (± recruiting share)

Sponsors near 19% open enrollment (± trial volume)

What to do with this Ipsen page

85 registered trials is a research-attention snapshot, not an endorsement of Ipsen or any single study.

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Ipsen pipeline card: 85 registered trials from official public datasets.Report a data error.