American Regent

Closed portfolio with a later-stage archive tilt

According to ClinicalTrials.gov-derived indexes, American Regent sits in the top decile of US sponsors by registered trial count (#484 of 15,742 sponsors by registered trial count).

34 total trials none currently recruiting 31 completed later-stage tilt top decile by trial count

American Regent: 34 sponsored US clinical trials, none currently recruiting.

American Regent sponsors 34 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 31 completed. 23 of these trials are in Phase 3-4 (later-stage) and 9 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Iron Deficiency Anemia, with 3 trials.

Top-decile sponsor footprint

American Regent ranks in the top decile of sponsors by registered trial count (#484 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

C 68/100

31 of 34 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (91.2%), 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.

Indexed trials (enrollment closed)

34 total, page 1 of 1

COMPLETED Phase 3

Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients With Iron Deficiency Anemia and Unsatisfactory Response Oral Iron Under Study Protocol 1VIT17044

NCT04269707

COMPLETED Phase 3

Multicenter Randomized Active-controlled Study to Investigate Efficacy & Safety of IV FCM in Pediatric Patients With IDA

NCT03523117

TERMINATED Phase 2

Randomized, Placebo-controlled Trial of Ferric Carboxymaltose in RLS Patients With Iron-deficiency Anemia

NCT02826681

COMPLETED Phase 3

Randomized Placebo-controlled Trial of FCM as Treatment for Heart Failure With Iron Deficiency / and Sub-Study

NCT03037931

COMPLETED Phase 3

Can Iron Lessen Anemia Due to Cancer and Chemotherapy: A Study to Investigate the Efficacy and Safety of Injectafer®

NCT02453334

COMPLETED Phase 2

Blinded Randomized Placebo-Controlled Study Efficacy and Safety of Injectafer in ID Patients With Fibromyalgia

NCT02409459

COMPLETED Phase 3

Placebo-Controlled Study to Investigate the Efficacy & Safety of Injectafer in the Treatment of RLS

NCT02397057

COMPLETED

Registry to Evaluate Maintenance Treatment With Venofer in Pediatric Patients With Chronic Kidney Disease

NCT02492672

COMPLETED

Observational Study on the Use of IV (Intravenous) Iron Therapy Among Subjects With Iron Deficiency Anemia

NCT01984554

COMPLETED Phase 3

Pharmacokinetics, Safety, and Efficacy of SPRIX in 12 to 17 Year Old Patients vs. Adult Patients Undergoing Open Surgical Procedures

NCT01819610

COMPLETED Phase 1

Blinded Cross-Over Bioequivalence (BE) Trial of Luitpold Azacitidine vs Vidaza

NCT01290302

COMPLETED Phase 3

Efficacy and Safety of Intravenous Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia (IDA)

NCT00982007

COMPLETED Phase 3

Evaluation of Efficacy and Safety of Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia and Impaired Renal Function

NCT00981045

COMPLETED Phase 2

Intravenous Ferric Carboxymaltose vs IV Iron Sucrose or IV Iron Dextran in Treating Iron Deficiency Anemia in Women

NCT01290315

COMPLETED Phase 3

Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Standard of Care in Treating Iron Deficiency Anemia

NCT00703937

COMPLETED Phase 3

Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Iron Dextran in Treating Iron Deficiency Anemia

NCT00704028

COMPLETED Phase 3

Safety and Tolerability of a Single Dose of FCM vs. Standard of Care in Treating Iron Deficiency Anemia

NCT00704353

COMPLETED Phase 1

Safety and Pharmacokinetics Study of Intranasal Ketorolac in Elderly and Nonelderly Adult Healthy Subjects

NCT01365624

COMPLETED Phase 3

Safety of FCM vs. Standard of Care in Treating Iron Deficiency Anemia in Heavy Uterine Bleeding and Post Partum Patients

NCT00548860

COMPLETED Phase 3

Safety and Tolerability of FCM vs Standard of Care in Treating Iron Deficiency Anemia in Chronic Kidney Disease Patients

NCT00548691

TERMINATED Phase 2

Taxoprexin® Treatment for Advanced Primary Cancers of the Liver, Gallbladder or Biliary Tract

NCT00422877

COMPLETED Phase 2

Intravenous Iron Metabolism in Restless Legs Syndrome

NCT00685815

COMPLETED Phase 3

Safety and Efficacy of a Hematinic Agent in the Treatment of Postpartum Patients

NCT00354484

COMPLETED Phase 2

Iron Sucrose in Non-Dialysis Dependent (NDD-CKD) Pediatric Patients

NCT00721188

COMPLETED Phase 3

Taxoprexin Plus Carboplatin Treatment for Advanced Lung Cancer

NCT00243867

COMPLETED Phase 2

Taxoprexin® Treatment for Advanced Eye Melanoma

NCT00244816

COMPLETED Phase 3

Safety and Tolerability of Intravenous VIT-45 in Patients With Iron Deficiency Anemia

NCT00740246

COMPLETED Phase 4

Safety and Efficacy of Iron Sucrose in Children

NCT00239642

COMPLETED Phase 3

Long Term Safety Study of (VIT45) Extension Study: Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease

NCT00317226

COMPLETED Phase 3

VIT45 Versus Oral Iron in the Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease

NCT00317239

COMPLETED Phase 3

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in the Treatment of Anemia Secondary to Heavy Uterine Bleeding

NCT00395993

COMPLETED Phase 3

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in Subjects Who Display Postpartum Anemia

NCT00396292

COMPLETED Phase 3

Comparison of Safety and Efficacy of Intravenous Iron Versus Oral Iron in Chronic Renal Failure Subjects With Anemia

NCT00236977

TERMINATED Phase 3

Study of Taxoprexin Injection vs. Dacarbazine in Patients With Metastatic Malignant Melanoma

NCT00087776

Phase Distribution

PhaseTrial count
Phase 1 2
Phase 2 7
Phase 3 22
Phase 4 1

How the American Regent archive is shaped

34 indexed studies, none listed as recruiting (0% open); 31 completed (91%).

Phase mix: 23 late (III/IV) vs 9 early (I/II) (later-stage heavy).

Top condition: Iron Deficiency Anemia (3 trials), 7 others listed.

How to read a closed sponsor archive

When recruiting_count is zero, the indexed set is completed or otherwise not open. Phase tilt still describes where archived studies sat on the investigational pathway. Re-check ClinicalTrials.gov before acting.

American Regent: archived-pipeline peers nationwide

Peers matched on 34 indexed studies with no current recruiting: volume and archive shape, not condition overlap.

American Regent 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 010203040 0%10%20%30%40%50% Total trials Recruiting share American RegentAllegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)Amicus TherapeuticsCochlearEmergent BioSolutions10xBio22nd Century Group23andMe3-C Institute for Social Development
American Regent 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).

American Regent 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 34 archived trials

Sponsors with similar archive density (± trial count)

What to do with this American Regent page

34 registered trials is a research-attention snapshot, not an endorsement of American Regent or any single study.

  • None of American Regent's trials are currently recruiting in this registry; that can change as new trials post, or check the broader research index. Browse research indexes
  • Iron Deficiency Anemia is the condition American Regent studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Iron Deficiency Anemia 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.

American Regent pipeline card: 34 registered trials from official public datasets.Report a data error.