Ferring Pharmaceuticals

Open enrollment across a mixed-phase pipeline

According to ClinicalTrials.gov-derived indexes, Ferring Pharmaceuticals sits in the top decile of US sponsors by registered trial count (#271 of 15,742 sponsors by registered trial count).

83 total trials 4 currently recruiting 68 completed top decile by trial count

Ferring Pharmaceuticals: 83 sponsored US clinical trials, 4 recruiting.

Ferring Pharmaceuticals sponsors 83 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 68 completed. 45 of these trials are in Phase 3-4 (later-stage) and 33 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Cervical Ripening, with 4 trials.

Top-decile sponsor footprint

Ferring Pharmaceuticals ranks in the top decile of sponsors by registered trial count (#271 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

D 55/100

68 of 79 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (86.1%), 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

83 total, page 1 of 2

RECRUITING Phase 1

Low-grade UTUC Treated With Nadofaragene Firadenovec Administered to Renal Pelvis

NCT06668493

RECRUITING Phase 3

Trial of Nadofaragene Firadenovec vs. Observation in Participants With Intermediate Risk Non-Muscle Invasive Bladder Cancer

NCT06510374

RECRUITING Phase 3

A Trial to Evaluate Intravesical Nadofaragene Firadenovec Alone or in Combination With Chemotherapy or Immunotherapy in Participants With High-grade BCG Unresponsive Non-muscle Invasive Bladder Cancer

NCT06545955

RECRUITING Phase 1

Study Assessing CLENPIQ as Bowel Preparation for Pediatric Colonoscopy

NCT04113382

TERMINATED

ADSTILADRIN Early Utilization and Outcomes in the Real World Setting

NCT06026332

COMPLETED

REBYOTA™ Prospective Registry

NCT05835219

COMPLETED Phase 1

A Study to Evaluate the Effect of Carbetocin on the QT/QTc Interval in Healthy Subjects

NCT05924321

COMPLETED Phase 3

A Multi-center, Single-arm Trial Exploring the Safety and Clinical Effectiveness of RBX2660 Administered by Colonoscopy to Adults With Recurrent Clostridioides Difficile Infection

NCT05831189

TERMINATED Phase 2

A Trial to Compare Efficacy and Safety of Follitropin Delta Versus Placebo (Inactive Treatment) in the Treatment of Men With Idiopathic Infertility (Unexplained Reduction of Semen Quality) (ADAM)

NCT05403476

TERMINATED Phase 2

Merotocin in Mothers With Inadequate Milk Production and Infants Delivered Prematurely

NCT02545127

COMPLETED Phase 3

Comparison of MENOPUR Liquid and Powder in Women Undergoing Assisted Reproductive Technology (ART)

NCT04163458

COMPLETED

A Cross-Functional, Population-Representative, Web-Based, Epidemiologic Study to Estimate the Prevalence and Burden of Nocturia Due to Nocturnal Polyuria in the US

NCT04125186

COMPLETED Phase 2

Randomized Trial Assessing Quinagolide Vaginal Ring for Endometriosis-related Pain

NCT03692403

COMPLETED Phase 3

Recombinant FSH Investigation in the Treatment of Infertility With Assisted Reproductive Technology (ART) (RITA-2)

NCT03738618

COMPLETED Phase 3

Recombinant FSH Investigation in the Treatment of Infertility With Assisted Reproductive Technology (ART) (RITA-1)

NCT03740737

COMPLETED Phase 3

Clinical Safety Study of the Progesterone Vaginal Ring in Women Undergoing Assisted Reproductive Technology Procedures

NCT03565211

COMPLETED NA

AMPLEX Ankle Fusion and Hindfoot

NCT03028415

COMPLETED Phase 2

A Trial to Investigate Efficacy, Safety and Tolerability of FE 201836 for Nocturia Due to Nocturnal Polyuria in Adults

NCT03201419

COMPLETED Phase 3

A Study Comparing the Sodium Picosulfate, Magnesium Oxide and Anhydrous Citric Acid Oral Solution With PREPOPIK® for Colon Cleansing in Preparation for Colonoscopy

NCT03017235

COMPLETED Phase 3

ADSTILADRIN (=INSTILADRIN) in Patients With High-Grade, Bacillus Calmette-Guerin (BCG) Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC)

NCT02773849

TERMINATED Phase 3

A Trial Comparing Cardiovascular Safety of Degarelix Versus Leuprolide in Patients With Advanced Prostate Cancer and Cardiovascular Disease

NCT02663908

COMPLETED Phase 3

Mesalamine 2 g Sachet for the Maintenance of Clinical and Endoscopic Remission in Ulcerative Colitis (UC)

NCT02522780

COMPLETED Phase 3

Mesalamine 4 g Sachet for the Induction of Remission in Active, Mild to Moderate Ulcerative Colitis (UC)

NCT02522767

COMPLETED Phase 4

MENOPUR® in a Gonadotropin-Releasing Hormone (GnRH) Antagonist Cycle With Single-Blastocyst Transfer in a High Responder Subject Population

NCT02554279

TERMINATED Phase 2

Selepressin Evaluation Programme for Sepsis-Induced Shock - Adaptive Clinical Trial

NCT02508649

COMPLETED Phase 3

A Clinical Trial to Evaluate the Efficacy and Safety of Testosterone Gel in Adult Hypogonadal Males

NCT02149264

COMPLETED Phase 1

Efficacy and Safety of Prepopik® in Children for Overall Colon Cleansing in Preparation for Colonoscopy

NCT01928862

COMPLETED Phase 3

LutrePulse Hypogonadotropic Hypogonadism

NCT01976728

COMPLETED Phase 2

Treatment of Hyperphagia Behavioral Symptoms in Children and Adults Diagnosed With Prader-Willi Syndrome

NCT01968187

COMPLETED Phase 3

Safety and Tolerability Extension Trial for Patients With Chronic Idiopathic Constipation

NCT01895543

TERMINATED Phase 3

26 Week Efficacy and Safety Trial for Patients With Chronic Idiopathic Constipation

NCT01827592

TERMINATED Phase 3

Efficacy and Safety Trial of Elobixibat in Patients With Chronic Idiopathic Constipation

NCT01833065

COMPLETED Phase 2

Interventional Clinical Trial in Patients in Overactive Bladder With Nocturia in Women

NCT01729819

COMPLETED Phase 3

A Multicenter Extension Trial to Evaluate the Safety of Testosterone Gel

NCT01703741

COMPLETED Phase 3

A Clinical Trial to Evaluate the Efficacy and Safety of Testosterone Gel

NCT01665599

COMPLETED Phase 3

Study Investigating the Impact Burden of Nocturia Using the Nocturia Impact Diary

NCT01552343

COMPLETED Phase 2

Intramuscular Injections of Degarelix Administered in 1-Month Dosing Regimens in Patients With Prostate Cancer

NCT01491971

COMPLETED Phase 2

A Clinical Study to Evaluate the Pharmacokinetics of Testosterone Gel Using an Applicator

NCT01464879

COMPLETED Phase 4

Menopur Mixed Protocol

NCT01417195

COMPLETED Phase 2

Pharmacokinetic (PK) Study of the 200 Microgram (mcg) Misoprostol Vaginal Insert (MVI 200) in Women at Term Gestation (The MVI-PK Study)

NCT01283022

COMPLETED Phase 2

Efficacy, Pharmacokinetics and Safety of Testosterone

NCT01370369

COMPLETED Phase 3

Investigation of the Superiority Effect of Orally Disintegrating Desmopressin Tablets to Placebo in Terms of Night Voids Reduction in Nocturia Adult Male Patients

NCT01262456

COMPLETED Phase 3

Investigation of the Superiority Effect of Desmopressin to Placebo in Terms of Night Voids Reduction in Nocturia Adult Female Patients

NCT01223937

TERMINATED Phase 3

A Degarelix Trial in Patients With Prostate Cancer

NCT01242748

COMPLETED Phase 3

Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery

NCT01127581

COMPLETED Phase 4

Lysteda Pediatric Research Equity Act (PREA) Pharmacokinetic Study in Adolescent Females With Heavy Menstrual Bleeding

NCT01190150

COMPLETED Phase 3

Investigation of PicoPrep Versus HalfLytely for Bowel Preparation for Colonoscopy - Split Dose PicoPrep

NCT01073930

COMPLETED Phase 3

Investigation of PicoPrep Versus HalfLytely for Bowel Preparation for Colonoscopy - Day Before PicoPrep

NCT01073943

COMPLETED Phase 2

Efficacy and Safety Study of the Misoprostol Vaginal Priming Insert (MVPI) Prior to Hysteroscopy

NCT00925938

COMPLETED Phase 2

Effects of the V1a Agonist FE 202158 in Patients With Septic Shock

NCT01000649

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What is open in the Ferring Pharmaceuticals pipeline

4 recruiting of 83 indexed (5% open); 68 completed (82%).

Phase mix: 45 late (III/IV) vs 33 early (I/II) (balanced across stages).

Top condition: Cervical Ripening (4 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.

Ferring Pharmaceuticals: open-pipeline peers nationwide

Peers matched on 83 registered trials and 5% open enrollment, not the therapeutic-area sidebar.

Ferring Pharmaceuticals 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 020406080100 0%10%20%30%40% Total trials Recruiting share Ferring PharmaceuticalsNational Jewish HealthNew York UniversityTeva Pharmaceuticals USASeagenAmphastar PharmaceuticalsCook County HealthDavid Grant U.S. Air Force Medical CenterDuquesne University
Ferring Pharmaceuticals 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).

Ferring Pharmaceuticals 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 83 trials (± recruiting share)

Sponsors near 5% open enrollment (± trial volume)

What to do with this Ferring Pharmaceuticals page

83 registered trials is a research-attention snapshot, not an endorsement of Ferring Pharmaceuticals or any single study.

  • 4 of Ferring Pharmaceuticals's trials are currently recruiting, check each one's own eligibility criteria before contacting a site. Browse recruiting trials
  • Cervical Ripening is the condition Ferring Pharmaceuticals studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Cervical Ripening trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

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

Ferring Pharmaceuticals pipeline card: 83 registered trials from official public datasets.Report a data error.