Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 55/100

Failure Rate

20.0%

3 terminated/withdrawn out of 15 trials

Success Rate

80.0%

-6.5% vs industry average

Late-Stage Pipeline

27%

4 trials in Phase 3/4

Results Transparency

58%

7 of 12 completed trials have results

Key Signals

7 with results

Enrollment Performance

Analytics

Phase 1
5(41.7%)
Phase 3
4(33.3%)
Phase 2
3(25.0%)
12Total
Phase 1(5)
Phase 3(4)
Phase 2(3)

Activity Timeline

Global Presence

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Clinical Trials (15)

Showing 15 of 15 trials
NCT03866577Phase 1Terminated

Safety and Tolerability of M254 in Healthy Volunteers and Immune Thrombocytopenic Purpura (ITP) Patients

Role: lead

NCT02921191Completed

Descriptive Analysis of G-CSF Use in Patients With Breast Cancer, Lung Cancer, or Lymphoma Treated

Role: collaborator

NCT02922192Completed

Incidence of Hospitalizations for Serious Infections in Patients Receiving Biologic Anti-Inflammatories for Rheumatologic, Psoriatic, and Gastrointestinal Conditions: A Descriptive Analysis

Role: collaborator

NCT03772587Phase 2Completed

A Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics and Pharmacodynamics of M281 Administered to Adults With Generalized Myasthenia Gravis

Role: lead

NCT03896295Phase 2Terminated

An Extension Study of MOM-M281-004 to Evaluate the Safety, Tolerability, and Efficacy of M281 Administered to Patients With Generalized Myasthenia Gravis

Role: lead

NCT03610646Phase 3Completed

Comparative Study to Evaluate the Efficacy and Safety of MYL-1701P and Eylea® in Subjects With Diabetic Macular Edema (DME)

Role: collaborator

NCT04674800Phase 3Completed

Extension Study of MYL-1701P-3001 for Safety and Efficacy

Role: collaborator

NCT02922179Completed

Descriptive Analysis of Long- and Intermediate-Acting Insulin in Adult Diabetics

Role: collaborator

NCT02675023Phase 1Completed

Assessment of Pharmacokinetics and Safety of M923 Administered Via Auto-injector or Prefilled Syringe, in Healthy Subjects

Role: lead

NCT00543400Phase 2Completed

Evaluation of M118 in Percutaneous Coronary Intervention (EMINENCE)

Role: lead

NCT02828046Phase 1Completed

An Ascending Dose Study to Evaluate M281 Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD)

Role: lead

NCT02581345Phase 3Completed

Phase 3 Study of M923 and Humira® in Subjects With Chronic Plaque-type Psoriasis

Role: lead

NCT01621243Phase 1Terminated

M402 in Combination With Nab-Paclitaxel and Gemcitabine in Pancreatic Cancer

Role: lead

NCT02722044Phase 3Completed

Usability of an AI for M923 in Subjects With Moderate to Severe RA

Role: lead

NCT02923583Phase 1Completed

Assessment of Pharmacokinetics (PK) and Safety of M834 and Orencia ®, in Healthy Subjects

Role: lead

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