Key Insights

Highlights

Success Rate

88% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

5.3%

1 terminated out of 19 trials

Success Rate

87.5%

+1.0% vs benchmark

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

0%

0 of 7 completed with results

Key Signals

88% success

Data Visualizations

Phase Distribution

17Total
P 1 (17)

Trial Status

Completed7
Recruiting5
Active Not Recruiting4
Not Yet Recruiting2
Terminated1

Trial Success Rate

87.5%

Benchmark: 86.5%

Based on 7 completed trials

Clinical Trials (19)

Showing 19 of 19 trials
NCT06898450Phase 1RecruitingPrimary

A Study to Assess the Safety, Tolerability, and Efficacy of NDI-219216 in Patients With Advanced Solid Tumors.

NCT07514975Phase 1Not Yet RecruitingPrimary

First-In-Human Study of KHN922 for Injection

NCT07190469Phase 1Recruiting

PQ203 in Advanced Malignant Tumors Including Triple Negative Breast Cancer

NCT06607939Phase 1RecruitingPrimary

ORB-021 In Patients With Advanced Solid Tumors

NCT02988960Phase 1Active Not RecruitingPrimary

A Study of ABBV-927 and ABBV-181, an Immunotherapy, in Participants With Advanced Solid Tumors

NCT07327489Recruiting

Predicting Response to Immunotherapy From Analysis of Live Tumor Biopsies

NCT07259590Phase 1RecruitingPrimary

A Study of GFH375 Combined With Cetuximab or Chemotherapy in Participants With Solid Tumors Harboring KRAS G12D Mutation

NCT04417465Phase 1CompletedPrimary

First In Human Study With ABBV-CLS-579 When Given Alone and In Combination In Participants With Locally Advanced Or Metastatic Tumors

NCT02099058Phase 1Active Not RecruitingPrimary

A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy of ABBV-399 in Participants With Advanced Solid Tumors

NCT07118709Phase 1Not Yet RecruitingPrimary

A Study of KC1086 in Patients With Advanced Solid Tumors

NCT04721015Phase 1Active Not RecruitingPrimary

Study of Intravenous (IV) ABBV-637 Alone or in Combination With IV Docetaxel/Osimertinib to Assess Adverse Events and Change in Disease Activity in Adult Participants With Relapsed/Refractory (R/R) Solid Tumors

NCT07035470CompletedPrimary

Biological Age Predicts 90-Day Mortality in Advanced Cancer

NCT03821935Phase 1Active Not RecruitingPrimary

Study to Determine the Safety, Tolerability, Pharmacokinetics and Recommended Phase 2 Dose (RP2D) of Livmoniplimab (ABBV-151) as a Single Agent and in Combination With Budigalimab (ABBV-181) in Participants With Locally Advanced or Metastatic Solid Tumors

NCT04196283Phase 1CompletedPrimary

A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ABBV-368 Plus Tilsotolimod and Other Therapy Combinations in Participants With Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma

NCT03071757Phase 1CompletedPrimary

A Study of the Safety, Tolerability and Pharmacokinetics of ABBV-368 as a Single Agent and Combination in Subjects With Locally Advanced or Metastatic Solid Tumors

NCT03234712Phase 1CompletedPrimary

A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABBV-321 in Subjects With Advanced Solid Tumors Associated With Overexpression of the Epidermal Growth Factor Receptor (EGFR)

NCT02955251Phase 1CompletedPrimary

A Study of ABBV-428, an Immunotherapy, in Subjects With Advanced Solid Tumors

NCT03311477Phase 1CompletedPrimary

A Study to Evaluate the Safety and Pharmacokinetics ABBV-399 in Japanese Participants With Solid Tumors

NCT03145909Phase 1TerminatedPrimary

A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV-176 in Subjects With Advanced Solid Tumors Likely to Express Prolactin Receptor (PRLR)

Showing all 19 trials

Research Network

Activity Timeline