Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 85/100

Failure Rate

17.6%

3 terminated/withdrawn out of 17 trials

Success Rate

50.0%

-36.5% vs industry average

Late-Stage Pipeline

6%

1 trials in Phase 3/4

Results Transparency

0%

0 of 3 completed trials have results

Key Signals

3 recruiting

Enrollment Performance

Analytics

Phase 1
11(64.7%)
Phase 2
5(29.4%)
Phase 3
1(5.9%)
17Total
Phase 1(11)
Phase 2(5)
Phase 3(1)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT06479135Phase 3Recruiting

Study of Navtemadlin add-on to Ruxolitinib in JAK Inhibitor-Naïve Patients With Myelofibrosis Who Have a Suboptimal Response to Ruxolitinib

Role: lead

NCT05797831Phase 2Recruiting

Study of Navtemadlin as Maintenance Therapy in TP53WT Advanced or Recurrent Endometrial Cancer

Role: lead

NCT04113616Phase 1Terminated

An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 When Administered Alone and in Combination With Low-Dose Cytarabine (LDAC) or Decitabine in Patients With Acute Myeloid Leukemia (AML)

Role: lead

NCT05705466Phase 1Withdrawn

Study of Navtemadlin Plus Pembrolizumab as Maintenance Therapy in Locally Advanced and Metastatic Non-Small Cell Lung Cancer

Role: lead

NCT05027867Phase 2Terminated

KRT-232 in Subjects With Relapsed or Refractory Small Cell Lung Cancer

Role: lead

NCT03662126Phase 2Unknown

KRT-232 Versus Best Available Therapy for the Treatment of Subjects With Myelofibrosis Who Are Relapsed or Refractory to JAK Inhibitor Treatment

Role: lead

NCT03787602Phase 1Unknown

Navtemadlin (KRT-232) With or Without Anti-PD-1/Anti-PD-L1 for the Treatment of Patients With Merkel Cell Carcinoma

Role: lead

NCT04669067Phase 1Unknown

TL-895 and KRT-232 Study in Acute Myeloid Leukemia

Role: collaborator

NCT04502394Phase 1Unknown

Safety and Efficacy of KRT-232 in Combination With Acalabrutinib in Subjects With R/R DLBCL or R/R CLL

Role: lead

NCT04640532Phase 1Unknown

KRT-232 in Combination With TL-895 for the Treatment of R/R MF and KRT-232 for the Treatment of JAKi Intolerant MF

Role: lead

NCT04878003Phase 2Unknown

Study of KRT-232 or TL-895 in Janus Associated Kinase Inhibitor Treatment-Naïve Myelofibrosis

Role: lead

NCT04485260Phase 1Unknown

An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 Combined With Ruxolitinib in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (Post-PV-MF), Or Post-Essential Thrombocythemia MF (Post ET-MF) Who Have a Suboptimal Response to Ruxolitinib

Role: lead

NCT04835584Phase 1Recruiting

KRT-232 and TKI Study in Chronic Myeloid Leukemia

Role: lead

NCT01723020Phase 1Completed

A Phase 1 Study Evaluating AMG 232 in Advanced Solid Tumors or Multiple Myeloma

Role: lead

NCT02110355Phase 1Completed

A Phase 1b/2a Study Evaluating AMG 232 in Metastatic Melanoma

Role: lead

NCT03669965Phase 2Unknown

KRT-232 Compared to Ruxolitinib in Patients With Phlebotomy-Dependent Polycythemia Vera

Role: lead

NCT02016729Phase 1Completed

A Phase 1b Study Evaluating AMG 232 Alone and in Combination With Trametinib in Acute Myeloid Leukemia

Role: lead

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