Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

10.7%

3 terminated/withdrawn out of 28 trials

Success Rate

86.4%

-0.1% vs industry average

Late-Stage Pipeline

25%

7 trials in Phase 3/4

Results Transparency

58%

11 of 19 completed trials have results

Key Signals

3 recruiting11 with results

Enrollment Performance

Analytics

Phase 1
11(45.8%)
Phase 3
7(29.2%)
Phase 2
6(25.0%)
24Total
Phase 1(11)
Phase 3(7)
Phase 2(6)

Activity Timeline

Global Presence

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Clinical Trials (28)

Showing 20 of 28 trials
NCT03541200Phase 2Completed

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

Role: lead

NCT03291067Phase 2Completed

MT-8554 for Reduction of Vasomotor Symptoms in Postmenopausal Women

Role: lead

NCT03809039Phase 1Terminated

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of MT-6345 in Healthy Subjects

Role: lead

NCT03840993Phase 2Completed

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

Role: lead

NCT03520036Phase 2Completed

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

Role: lead

NCT04569084Phase 3Terminated

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

Role: lead

NCT04402489Phase 3Completed

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

Role: lead

NCT04440592Phase 2Completed

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

Role: lead

NCT05151471Phase 3Terminated

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

Role: lead

NCT04577404Phase 3Completed

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

Role: lead

NCT04165824Phase 3Completed

Safety Study of Oral Edaravone Administered in Subjects With ALS

Role: lead

NCT03381404Phase 1Completed

Mass Balance Study With MT-8554

Role: lead

NCT03471130Phase 1Completed

Definitive QT Study With MT-8554

Role: lead

NCT04683848Phase 2Completed

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

Role: lead

NCT05005975Phase 3Recruiting

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

Role: lead

NCT06144840Phase 3Active Not Recruiting

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

Role: lead

NCT06943521Phase 1Recruiting

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

Role: lead

NCT05067179Recruiting

Analysis of Human ALS Tissues and Registry of ALS Patients

Role: collaborator

NCT05276349Completed

Home-based Remote Digital Monitoring to Assess ALS Progression (Track ALS)

Role: collaborator

NCT04259255Unknown

Radicava® (Edaravone) Findings in Biomarkers From ALS (REFINE-ALS)

Role: lead