Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

9.1%

2 terminated/withdrawn out of 22 trials

Success Rate

90.0%

+3.5% vs industry average

Late-Stage Pipeline

18%

4 trials in Phase 3/4

Results Transparency

39%

7 of 18 completed trials have results

Key Signals

7 with results

Enrollment Performance

Analytics

Phase 1
13(59.1%)
Phase 2
5(22.7%)
Phase 3
3(13.6%)
Phase 4
1(4.5%)
22Total
Phase 1(13)
Phase 2(5)
Phase 3(3)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (22)

Showing 20 of 22 trials
NCT04360681Phase 2Completed

Lofexidine Combined With Buprenorphine for Reducing Symptoms of PTSD and OU Relapse in Veterans

Role: collaborator

NCT05993299Phase 2Active Not Recruiting

Study to Evaluate Safety and Antitumor Activity of Lete-Cel (GSK3377794) in HLA-A2+ Participants With NY-ESO-1 Positive Previously Untreated Advanced (Metastatic or Unresectable) Synovial Sarcoma and Myxoid/Round Cell Liposarcoma

Role: lead

NCT07321912Phase 2Not Yet Recruiting

Eflornithine (DFMO) for Ewing Sarcoma and Osteosarcoma

Role: collaborator

NCT06711640Phase 1Withdrawn

A Pharmacokinetic, Safety, and Tolerability Study of LUCEMYRA in the Treatment of Opioid Withdrawal Management in Adolescent Subjects

Role: lead

NCT04070157Phase 2Terminated

Randomized, Double-Blind, Placebo-Controlled Pilot Study on the Safety and Effectiveness of LUCEMYRA During an Opioid Taper in Treatment of Withdrawal

Role: lead

NCT04188730Phase 1Completed

A Study Evaluating the Relative Bioavailability of Lofexidine Granules for Reconstitution Compared to LUCEMYRA (Lofexidine) Tablets and the Effect of Food on the Bioavailability of the Lofexidine Granules for Reconstitution

Role: lead

NCT02363998Phase 3Completed

Open-Label, Safety Study of Lofexidine

Role: lead

NCT01863186Phase 3Completed

Efficacy, Safety and Dose-Response Study Followed by Open-Label Study of Lofexidine Treatment of Opioid Withdrawal

Role: lead

NCT04126083Phase 4Completed

Lofexidine for Adults Undergoing Lumbar Spine Surgery

Role: collaborator

NCT04056182Phase 2Completed

Lofexidine for Management of Opioid Withdrawal With XR-NTX Treatment

Role: collaborator

NCT02318836Phase 1Completed

Single-Dose Pharmacokinetics and Safety of Oral Lofexidine in Hepatically-Impaired Subjects

Role: lead

NCT02681198Phase 1Completed

Lofexidine Pharmacokinetics in the Presence of Paroxetine in Healthy Volunteers

Role: lead

NCT01558934Phase 1Completed

Pilot Study of Lofexidine and Methadone Pharmacodynamic Interaction in Methadone Maintained Patients

Role: lead

NCT01820442Phase 1Completed

Pharmacokinetic & Pharmacodynamic Interaction of Lofexidine and Buprenorphine in Buprenorphine Maintained Patients

Role: lead

NCT01437306Phase 1Completed

Lofexidine Food Effect Study in Healthy Volunteers

Role: lead

NCT01629446Phase 1Completed

Lofexidine Mass Balance in Volunteers

Role: lead

NCT01650649Phase 1Completed

Main Study of Lofexidine and Methadone Pharmacodynamic Interaction in Methadone Maintained Patients

Role: lead

NCT02313103Phase 1Completed

Single-dose Pharmacokinetics and Safety of Oral Lofexidine in Renally-Impaired Subjects

Role: lead

NCT02446002Phase 1Completed

Assessment of the Effect of Naltrexone on Lofexidine Single Dose Pharmacokinetics in Healthy Subjects

Role: lead

NCT01310296Phase 1Completed

Lofexidine ADME & Mass Balance in Volunteers

Role: lead