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Janssen Infectious Diseases BVBA
Industry · 14 registered clinical trials.
Status
Trial
Phase
Started
Completed
A Study to Evaluate the Pharmacokinetic Effects of Different Storage Conditions for a Long-Acting Nanosuspensi
Human Immunodeficiency Virus Type 1
Phase 1
2015-08-14
Completed
A Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-63623872 in Healthy Japanese Adult Pa
Healthy
Phase 1
2015-05-01
Completed
A Study to Assess the Drug-Drug Interaction Between VX-787 and Oseltamivir
Healthy
Phase 1
2014-07-01
Completed
Efficacy and Safety Study of Simeprevir in Combination With Sofosbuvir in Participants With Chronic Hepatitis
Hepatitis C Virus Infection
Phase 3
2014-04-01
Completed
Efficacy and Safety Study of Simeprevir in Combination With Sofosbuvir in Participants With Genotype 1 Chronic
Hepatitis C Virus Infection
Phase 3
2014-04-01
Withdrawn
A Study to Evaluate the Efficacy and Safety of TMC207 in Patients With Pulmonary Infection With Multi-drug Res
Multi-drug Resistant Tuberculosis
Phase 3
2014-03-01
Completed
A Study to Assess the Relative Bioavailability of TMC207 Following Single-Dose Administrations of Two Pediatri
Healthy, Biological Availability
Phase 1
2013-04-01
Completed
A Study to Assess Safety and Pharmacokinetics of Telaprevir in Patients With Hepatic Impairment
Hepatic Impairment
Phase 1
2012-06-01
Completed
A Study to Investigate the Potential Pharmacokinetic Interactions Between Phenytoin or Carbamazepine and Telap
Healthy Participants
Phase 1
2012-05-01
Completed
VX-950-C211 - A Dosing Regimen Study (Twice Daily Versus Every 8 Hours) of Telaprevir in Treatment-naïve Parti
Genotype 1 Chronic Hepatitis C, Treatment Naive
Phase 3
2010-12-01
Completed
VX-950-TiDP24-C219: A Roll Over Trial for Patients in the Control Group of the C216 Study Who Received Telapre
Hepatitis C, Chronic
Phase 3
2010-04-01
Completed
To Evaluate the Safety, Tolerability, and Efficacy of TMC207 as Part of an Individualized Multi-drug Resistant
Tuberculosis
Phase 2
2009-09-01
Completed
TMC207-TiDP13-C208: Anti-bacterial Activity, Safety, and Tolerability of TMC207 in Participants With Multi-dru
Tuberculosis
Phase 2
2007-06-01
Approved For Marketing
Early Access of TMC207 in Patients With Extensively Drug Resistant or Pre-XDR Pulmonary Tuberculosis
Tuberculosis
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