Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 75/100

Failure Rate

16.2%

6 terminated/withdrawn out of 37 trials

Success Rate

82.9%

-3.6% vs industry average

Late-Stage Pipeline

5%

2 trials in Phase 3/4

Results Transparency

24%

7 of 29 completed trials have results

Key Signals

7 with results

Enrollment Performance

Analytics

Phase 1
24(68.6%)
Phase 2
9(25.7%)
Phase 3
2(5.7%)
35Total
Phase 1(24)
Phase 2(9)
Phase 3(2)

Activity Timeline

Global Presence

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Clinical Trials (37)

Showing 20 of 37 trials
NCT03162536Phase 1Active Not Recruiting

A Study of Nemtabrutinib (MK-1026) in Participants With Relapsed or Refractory Hematologic Malignancies (ARQ 531-101/MK-1026-001)

Role: lead

NCT01752920Phase 1Completed

Phase 1/2 Study of Derazantinib (ARQ 087) in Adult Subjects With Advanced Solid Tumors With FGFR Genetic Alterations

Role: collaborator

NCT02761694Phase 1Terminated

Vevorisertib (ARQ 751) as a Single Agent or in Combination With Other Anti-Cancer Agents, in Solid Tumors With PIK3CA / AKT / PTEN Mutations (MK-4440-001)

Role: lead

NCT03094832Phase 1Terminated

Study of Miransertib (MK-7075) in Participants With PIK3CA-related Overgrowth Spectrum and Proteus Syndrome (MOSAIC) (MK-7075-002)

Role: lead

NCT03317366Unknown

Expanded Access to Provide ARQ 092 for the Treatment of Overgrowth Diseases and/or Vascular Anomalies

Role: lead

NCT01755767Phase 3Completed

Study of Tivantinib in Subjects With Inoperable Hepatocellular Carcinoma (HCC) Who Have Been Treated With One Prior Therapy

Role: collaborator

NCT01244191Phase 3Terminated

Tivantinib Plus Erlotinib Versus Placebo Plus Erlotinib for the Treatment of Non-squamous, Non-small-cell Lung Cancer

Role: collaborator

NCT01178411Phase 1Completed

An Extension Protocol for Subjects Who Were Previously Enrolled in Other Tivantinib (ARQ 197) Protocols

Role: lead

NCT02476955Phase 1Terminated

Open-label Phase 1b Study of ARQ 092 in Combination With Anastrozole

Role: lead

NCT01502800Phase 1Completed

Clinical Trial of ARQ 761 in Advanced Solid Tumors

Role: collaborator

NCT01149720Phase 1Completed

Determination of the Relative Bioavailability of ARQ 197 Tablet Formulation With Capsule C Formulation as a Reference in Subjects With Advanced Solid Tumors

Role: collaborator

NCT01395758Phase 2Completed

Erlotinib Plus Tivantinib (ARQ 197) Versus Single Agent Chemotherapy in Locally Advanced or Metastatic Non-Small Cell Lung Cancer

Role: lead

NCT01473095Phase 1Completed

Phase 1 Dose Escalation Study of ARQ 092 in Adult Subjects With Advanced Solid Tumors and Recurrent Malignant Lymphoma

Role: lead

NCT02762721Completed

Analysis of Oncogenes in Intrahepatic Cholangiocarcinoma or Mixed Hepatocellular-Cholangiocarcinoma in Tumor Tissue Samples

Role: lead

NCT00398840Phase 1Terminated

A Study of ARQ 171 in Patients With Advanced Solid Tumors

Role: lead

NCT00827177Phase 1Completed

Dose Escalation Study of ARQ 197 in Combination With Sorafenib in Adult Patients With Advanced Solid Tumors

Role: lead

NCT01070290Phase 2Withdrawn

A Study of ARQ 197 Versus Investigator's Choice of Second-Line Chemotherapy in Patients With Locally Advanced or Metastatic Gastric Cancer Who Have Progressive Neoplastic Disease Following Treatment With One Prior Chemotherapy Regimen

Role: lead

NCT01225536Phase 1Completed

Dose Escalation Study of ARQ 736 in Adult Subjects With Advanced Solid Tumors Harboring BRAF and/or NRAS Mutations

Role: lead

NCT00777309Phase 2Completed

A Randomized Phase 2 Study of Erlotinib + ARQ 197 Versus Erlotinib + Placebo in Previously Treated Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

Role: lead

NCT00622063Phase 1Completed

An Extension Study for Patients Previously Treated With ARQ 501

Role: lead