Astellas Pharma

165 total trials 2 currently recruiting 143 completed

Astellas Pharma sponsors 165 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 143 completed. 47 of these trials are in Phase 3-4 (later-stage) and 113 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Candidemia, with 4 trials.

Trial Pipeline

165 total, page 3 of 4

COMPLETED

Pilot Trial in Sleep Laboratory Setting to Compare the Physiology of Night Time Bladder Function in Subjects With Overactive Bladder (OAB) Versus Subjects That Have Insomnia and Healthy Normal Subjects

NCT01029015

COMPLETED Phase 1

A Study to Assess Pharmacokinetic Interaction of Multiple Dose Ketoconazole on Single Dose YM178 Oral Controlled Absorption System (OCAS) in Healthy Adult Volunteers

NCT01476800

COMPLETED Phase 4

A Study to Evaluate Solifenacin Succinate in Combination With Tamsulosin for the Treatment of Residual Overactive Bladder Symptoms (OAB) in Men.

NCT00333112

COMPLETED Phase 1

Phase 1 Study of OSI-930 in Cancer Patients

NCT00513851

COMPLETED Phase 2

An Extension Study Administering YM155 to Subjects Previously Enrolled in Another Protocol Administering YM155

NCT00818480

COMPLETED Phase 2

Cytomegalovirus (CMV) Vaccine in Donors and Recipients Undergoing Allogeneic Hematopoietic Cell Transplant (HCT)

NCT00285259

COMPLETED Phase 3

A Study to Assess the Long-Term Safety of Tacrolimus Cream in the Treatment of Psoriasis

NCT00293917

COMPLETED Phase 2

A Study for the Treatment of Unresectable Stage III or Metastatic Stage IV Melanoma

NCT00281541

COMPLETED Phase 3

Study of RSD1235 to Evaluate Safety in Patients With Atrial Fibrillation

NCT00281554

COMPLETED Phase 2

A Study of the Safety and Efficacy of Tacrolimus Inhalation Aerosol in Subjects With Persistent Asthma

NCT00116103

COMPLETED Phase 4

Safety/Efficacy of Induction Agents With Tacrolimus, MMF, and Rapid Steroid Withdrawal in Renal Transplant Recipients

NCT00113269

COMPLETED Phase 4

A Safety and Efficacy Study of Prograf in the Prevention of Erectile Dysfunction After Radical Prostatectomy

NCT00106392

TERMINATED Phase 2

Study of FK778 in Renal Transplant Recipients With Untreated BK Nephropathy

NCT00104338

COMPLETED Phase 4

A Multi-Center Study of Short and Long-term Use of Protopic Ointment in Patients With Atopic Dermatitis

NCT00106496

COMPLETED Phase 3

Study of Micafungin in Patients With Invasive Candidiasis or Candidemia

NCT00105144

COMPLETED Phase 4

Study of the Safety and Efficacy of Tacrolimus Ointment in Treating Chronic Allergic Contact Dermatitis

NCT00667056

COMPLETED Phase 4

Community Based Trial for AMEVIVE®

NCT00168753

TERMINATED Phase 2

A Randomized Study to Evaluate FK962 in Subjects With Mild to Moderate Alzheimer's Disease

NCT00087724

COMPLETED Phase 3

Study to Determine the Response and Effectiveness of RSD1235 in Subjects With Atrial Fibrillation or Atrial Flutter

NCT00115791

COMPLETED Phase 3

Open-label Study of the Efficacy and Safety of VESIcare® in Patients With Overactive Bladder Symptoms

NCT00463541

COMPLETED Phase 3

Efficacy & Safety Study of VESIcare® (Solifenacin Succinate) in Patients Wishing to Switch From Detrol LA® for Treatment of Overactive Bladder

NCT00454740

COMPLETED Phase 3

Response to RSD1235 Compared to Placebo in Subjects With Atrial Arrhythmia After Heart Surgery

NCT00125320

COMPLETED Phase 3

Canadian Cardiology de Novo Study: A Comparison Between Tacrolimus- and Cyclosporine- Based Immunoprophylactic Regimens

NCT00157014

COMPLETED Phase 3

A Multicenter VESIcare® Efficacy and Safety Study for the Treatment of Urgency Associated With Overactive Bladder (OAB)

NCT00454896

COMPLETED Phase 2

YM443 in Subjects With Functional Dyspepsia

NCT00102310

COMPLETED Phase 2

A Study of a Modified-Release Tacrolimus Based Immunosuppression Regimen in Stable Pediatric Liver Transplant Patients

NCT00282256

TERMINATED

AMEVIVE® Pregnancy Registry

NCT00342862

TERMINATED Phase 2

A Study to Evaluate the Safety and Efficacy of Prograf/FK778 and Prograf/MMF in de Novo Kidney Transplant Recipients

NCT00282230

COMPLETED Phase 3

A Study to Assess the Efficacy and Safety of Alefacept in Psoriasis Patients for Whom Conventional Treatment is Ineffective or Inappropriate

NCT00673556

COMPLETED Phase 2

A Placebo-controlled Study With an Extension Examining the Safety and Efficacy of Alefacept in Psoriatic Arthritis

NCT00659412

COMPLETED Phase 3

A Study to Assess the Efficacy and Safety of Two Dosing Regimens of Alefacept in Subjects Weighing Between 100kg and 150kg With Moderate to Severe Chronic Plaque Psoriasis

NCT00674063

COMPLETED Phase 3

Comparative Study of Modified Release (MR) Tacrolimus/Mycophenolate Mofetil (MMF) in de Novo Kidney Transplant Recipients

NCT00064701

TERMINATED

Assessment and Tracking of Long-term Alefacept Safety

NCT00454701

COMPLETED Phase 2

A Study to Assess the Pharmacokinetics of a Modified-release Tacrolimus Based Immunosuppression Regimen in Stable Liver Transplant Patients

NCT00282243

COMPLETED Phase 4

Optimizing Prograf® Therapy in Renal Transplant Patients

NCT00297765

COMPLETED Phase 3

Micafungin Versus AmBisome in Invasive Candidiasis and Candidemia

NCT00106288

TERMINATED Phase 3

Comparative Study of Micafungin (FK463) Versus Placebo as Prophylactic Antifungal Therapy in the ICU

NCT00048750

TERMINATED Phase 2

CP-461 in the Treatment of Patients With Advanced Melanoma

NCT00060710

COMPLETED Phase 4

Comparison Study Between Protopic (Tacrolimus Ointment) and Elidel (Pimecrolimus Cream) in Treating Pediatric Patients With Atopic Dermatitis

NCT00666159

COMPLETED Phase 4

Comparison Study Between Protopic (Tacrolimus Ointment) and Elidel (Pimecrolimus Cream) in Pediatric Patients With Mild Atopic Dermatitis

NCT00667160

TERMINATED Phase 2

Trial of Micafungin (FK463) in Combination With Liposomal Amphotericin B (AmBisome) for Aspergillosis

NCT00047827

COMPLETED Phase 2

Study of FK788 in Subjects With Chronic Hepatitis C Virus Infection

NCT00047814

COMPLETED Phase 4

A Comparison Study Between Protopic (Tacrolimus) Ointment and Elidel (Pimecrolimus) Cream in Treating Subjects With Atopic Dermatitis

NCT00666302

COMPLETED Phase 2

Study of OSI-211 vs. Topotecan in Patients With Relapsed Epithelial Ovarian Cancer

NCT00046800

COMPLETED Phase 2

Efficacy and Safety Study of OSI-211 (Liposomal Lurtotecan) to Treat Recurrent Small Cell Lung Cancer

NCT00046787

COMPLETED Phase 2

A Study to Assess the Pharmacokinetics of a Modified-release Tacrolimus Based Immunosuppression Regimen in Stable Kidney Transplant Patients

NCT00282568

COMPLETED Phase 2

CP-461 for the Treatment of Crohn's Disease

NCT00042055

COMPLETED Phase 1

Dose-Escalating and Safety Study of CP-461 in Patients With Chronic Lymphocytic Leukemia

NCT00036257

COMPLETED Phase 3

Study to Assess Efficacy of Tacrolimus + Methotrexate Versus Placebo + Methotrexate in Treatment of Rheumatoid Arthritis

NCT00036153

COMPLETED Phase 2

Trial of FK614 in Type 2 Diabetics Inadequately Controlled on a Sulfonylurea

NCT00036192

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Phase Distribution

PhaseTrial count
Phase 1 59
Phase 2 54
Phase 3 28
Phase 4 19

What the Pipeline for Astellas Pharma Shows

According to the ClinicalTrials.gov registry, Astellas Pharma is linked to 165 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 1% of the sponsor's indexed portfolio, and 143 are already marked complete, representing roughly 87% of the total.

The phase mix for Astellas Pharma reports 47 late-stage studies (Phase 3 and Phase 4 combined) and 113 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Astellas Pharma is Candidemia with 4 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.