Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 65/100

Failure Rate

21.4%

3 terminated/withdrawn out of 14 trials

Success Rate

78.6%

-7.9% vs industry average

Late-Stage Pipeline

7%

1 trials in Phase 3/4

Results Transparency

55%

6 of 11 completed trials have results

Key Signals

6 with results

Enrollment Performance

Analytics

Phase 2
6(46.2%)
Phase 1
6(46.2%)
Phase 3
1(7.7%)
13Total
Phase 2(6)
Phase 1(6)
Phase 3(1)

Activity Timeline

Global Presence

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Clinical Trials (14)

Showing 14 of 14 trials
NCT03028740Phase 3Terminated

AURORA: A Study for the Efficacy and Safety of Cenicriviroc (CVC) for the Treatment of Liver Fibrosis in Adults With Nonalcoholic Steatohepatitis (NASH)

Role: lead

NCT03059446Phase 2Terminated

Rollover Study of Cenicriviroc for the Treatment of Liver Fibrosis in Participants With Nonalcoholic Steatohepatitis

Role: lead

NCT02128828Phase 2Completed

Effect of Cenicriviroc on HIV Neurocognitive Impairment

Role: collaborator

NCT02330549Phase 2Completed

ORION: Effects of Cenicriviroc on Insulin Sensitivity in Subjects With Prediabetes or Type 2 Diabetes Mellitus (T2DM) and Suspected NAFLD

Role: lead

NCT02217475Phase 2Completed

Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Participants With Liver Fibrosis

Role: lead

NCT02653625Phase 2Completed

PERSEUS: Preliminary Efficacy and Safety of Cenicriviroc in Adult Participants With Primary Sclerosing Cholangitis

Role: lead

NCT02685462Phase 1Completed

Pharmacokinetic and Safety Study of Cenicriviroc and HMG-CoA Reductase Inhibitors, Caffeine and Digoxin

Role: lead

NCT02684799Phase 1Completed

Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination

Role: lead

NCT01474954Terminated

Investigation of The Effect of Cenicriviroc (CVC) Plus FTC/TDF on Cardiovascular Disease Risk Factors

Role: collaborator

NCT02342067Phase 1Completed

Pharmacokinetic and Safety Study of Cenicriviroc and Pioglitazone, When Dosed Alone or in Combination

Role: lead

NCT02120547Phase 1Completed

Phase 1 Study of Multiple-Dose Pharmacokinetics of Cenicriviroc in Subjects With Mild and Moderate Hepatic Impairment

Role: lead

NCT01827540Phase 1Completed

Study of Dolutegravir (DTG) on PK of Cenicriviroc (CVC), and CVC on PK of DTG & on a Single Dose of Midazolam

Role: lead

NCT01092104Phase 1Completed

A Proof of Concept Study to Evaluate the Antiviral Activity, Safety, and Pharmacokinetics of the CCR5 Antagonist TBR 652 in HIV 1-Infected, Antiretroviral Treatment-Experienced, CCR5 Antagonist-Naïve Patients

Role: lead

NCT01338883Phase 2Completed

Efficacy, Safety, and Tolerability of Cenicriviroc (CVC) in Combination With Truvada or Sustiva Plus Truvada in HIV 1-infected, Antiretroviral Treatment-naïve, Adult Patients Infected With Only CCR5-tropic Virus

Role: lead

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