Tanabe Pharma America

18 total trials 2 currently recruiting 13 completed

Tanabe Pharma America sponsors 18 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 13 completed. 7 of these trials are in Phase 3-4 (later-stage) and 11 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Menopause Hot Flashes, with 1 trials.

Trial Pipeline

18 total, page 1 of 1

RECRUITING Phase 1

A Study of MT-4561 in Patients With Various Advanced Solid Tumors

NCT06943521

RECRUITING Phase 3

Extension Study to Evaluate Safety and Tolerability of Oral Dersimelagon (MT-7117) in Subjects With Erythropoietic Protoporphyria (EPP) or X-Linked Protoporphyria (XLP)

NCT05005975

ACTIVE NOT RECRUITING Phase 3

INcreased Sun Exposure Without Pain In Research Participants With EPP or XLP

NCT06144840

COMPLETED Phase 1

Study to Evaluate the Effect of a Single Oral Dose of MT-7117 on the QT/QTc Interval in Healthy Subjects

NCT05241535

TERMINATED Phase 3

Efficacy and Safety Extension Study of Oral Edaravone Administered in Subjects With ALS

NCT05151471

COMPLETED Phase 2

Study to Assess the Efficacy and Safety of MT-3921 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

NCT04683848

COMPLETED Phase 1

Study to Investigate Drug-Drug Interaction Between MT-7117 and Test Drugs in Healthy Subjects

NCT04793295

COMPLETED Phase 2

Study to Evaluate Efficacy, Safety, and Tolerability of MT-7117 in Subjects With Diffuse Cutaneous Systemic Sclerosis

NCT04440592

TERMINATED Phase 3

Efficacy and Safety Study of Oral Edaravone Administered in Subjects With ALS

NCT04569084

COMPLETED Phase 3

Safety Extension Study of Oral Edaravone Administered in Subjects With Amyotrophic Lateral Sclerosis (ALS)

NCT04577404

COMPLETED Phase 3

Study to Evaluate Efficacy, Safety, and Tolerability of MT-7117 in Subjects With Erythropoietic Protoporphyria or X-Linked Protoporphyria

NCT04402489

COMPLETED Phase 1

Safety and Pharmacokinetics Study of MT-3921 in Spinal Cord Injury

NCT04096950

COMPLETED Phase 3

Safety Study of Oral Edaravone Administered in Subjects With ALS

NCT04165824

COMPLETED Phase 1

Study to Assess Pharmacokinetics, Safety, and Tolerability of MT-7117 in Subjects With Normal and Impaired Hepatic Function

NCT04116476

COMPLETED Phase 2

Safety and Efficacy Study of MT-2990 in Women With Endometriosis

NCT03840993

COMPLETED Phase 2

Study to Evaluate Efficacy, Safety, and Tolerability of MT-7117 in Subjects With Erythropoietic Protoporphyria

NCT03520036

COMPLETED Phase 2

Long-term Safety and Efficacy Study of MT-8554 in Postmenopausal Women With Vasomotor Symptoms

NCT03541200

COMPLETED Phase 2

MT-8554 for Reduction of Vasomotor Symptoms in Postmenopausal Women

NCT03291067

What the Pipeline for Tanabe Pharma America Shows

According to the ClinicalTrials.gov registry, Tanabe Pharma America is linked to 18 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 11% of the sponsor's indexed portfolio, and 13 are already marked complete, representing roughly 72% of the total.

The phase mix for Tanabe Pharma America reports 7 late-stage studies (Phase 3 and Phase 4 combined) and 11 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Tanabe Pharma America is Menopause Hot Flashes with 1 linked trial, 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.