Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

39.4%

13 terminated/withdrawn out of 33 trials

Success Rate

58.1%

-28.4% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

83%

15 of 18 completed trials have results

Key Signals

15 with results10 terminated

Enrollment Performance

Analytics

Phase 1
21(65.6%)
Phase 2
11(34.4%)
32Total
Phase 1(21)
Phase 2(11)

Activity Timeline

Global Presence

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Clinical Trials (33)

Showing 20 of 33 trials
NCT05521997Phase 2Not Yet Recruiting

Glutaminase Inhibition and Chemoradiation in Advanced Cervical Cancer

Role: collaborator

NCT03263429Phase 1Completed

Novel PET/CT Imaging Biomarkers of CB-839 in Combination With Panitumumab and Irinotecan in Patients With Metastatic and Refractory RAS Wildtype Colorectal Cancer

Role: collaborator

NCT03097328Phase 2Completed

Study of TAK-228 In Patients With Previously Treated Metastatic Renal Cell Carcinoma

Role: collaborator

NCT05319028Phase 2Terminated

Study of Mivavotinib (CB-659) in Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL)

Role: lead

NCT03428217Phase 2Completed

CANTATA: CB-839 With Cabozantinib vs. Cabozantinib With Placebo in Patients With Metastatic Renal Cell Carcinoma

Role: lead

NCT02771626Phase 1Terminated

Study CB-839 in Combination With Nivolumab in Patients With Melanoma, Clear Cell Renal Cell Carcinoma (ccRCC) and Non-Small Cell Lung Cancer (NSCLC)

Role: lead

NCT04698681Terminated

NGS Screening Protocol to Detect Mutation of KEAP1 or NRF2/NFE2L2 Genes for the KEAPSAKE (CX-839-014) Trial

Role: lead

NCT03357627Phase 1Completed

A Study of TAK-659 in Combination With Venetoclax for Adult Participants With Previously Treated Non-Hodgkin Lymphoma

Role: lead

NCT02834247Phase 1Terminated

A Study of TAK-659 in Combination With Nivolumab in Participants With Advanced Solid Tumors

Role: lead

NCT02000934Phase 1Completed

A Study of TAK-659 in Adult Participants With Advanced Solid Tumor and Lymphoma Malignancies

Role: lead

NCT02323113Phase 1Terminated

Safety, Tolerability, and Efficacy of TAK-659 in Adults With Relapsed or Refractory Acute Myelogenous Leukemia (AML)

Role: lead

NCT03238651Phase 1Terminated

A Study of TAK-659 as a Single Agent in Adult East Asian Participants With Non-Hodgkin Lymphoma (NHL)

Role: lead

NCT02756364Phase 2Completed

Sapanisertib in Combination With Fulvestrant in Women With Advanced or Metastatic Breast Cancer After Aromatase Inhibitor Therapy

Role: lead

NCT03338881Phase 1Withdrawn

A Study to Assess Mass Balance, Pharmacokinetics (PK), and Metabolism of Orally Administered [14 C]-TAK-659 in Participants With Advanced Solid Tumor and/or Lymphoma Malignancies

Role: lead

NCT03772288Phase 1Withdrawn

A Study of TAK-659 in Combination With NKTR-214 in Participants With Advanced Non-Hodgkin Lymphoma (NHL)

Role: lead

NCT03123393Phase 2Terminated

TAK-659 in Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL)

Role: lead

NCT03359733Phase 1Withdrawn

A Study to Evaluate the Effect of Food on the Pharmacokinetics (PK) of TAK-659 in Participants With Advanced Solid Tumor

Role: lead

NCT02049957Phase 2Completed

Safety and Efficacy Study of Sapanisertib in Combination With Exemestane or Fulvestrant in Postmenopausal Women With Estrogen Receptor Positive/Human Epidermal Growth Factor Receptor 2 Negative (ER+/HER2-) Metastatic Breast Cancer

Role: lead

NCT03370302Phase 1Terminated

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics (PK) of TAK-228 as Single Agent in Adult East Asian Participants With Advanced Nonhematological Malignancies

Role: lead

NCT02197572Phase 1Completed

Effect of Sapanisertib (MLN0128) on the QTc Interval in Participants With Advanced Solid Tumors

Role: lead