Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02592057
Other study ID # GS-US-334-1775
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 30, 2015
Est. completion date April 23, 2018

Study information

Verified date May 2018
Source Gilead Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will evaluate the safety and efficacy of sofosbuvir (SOF)-based regimens administered as per the approved prescribing information in adults with chronic hepatitis C virus (HCV) infection treated in routine clinical practice in India.


Recruitment information / eligibility

Status Completed
Enrollment 532
Est. completion date April 23, 2018
Est. primary completion date November 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- HCV-infected patients living in India

- Treatment with a SOF-based regimen as determined by the patient's treating physician per the approved prescribing information.

- Patients who provide written and signed informed consent prior to initiation of treatment where required.

Exclusion Criteria:

- Concurrent participation in an HCV clinical trial (except trials not testing investigational medicinal products)

- Patients presenting a risk of not being able to be followed (eg, patients planning to move or leave the country in a foreseeable future)

Study Design


Intervention

Drug:
SOF
SOF tablets administered orally once daily based on approved prescribing information

Locations

Country Name City State
India Sanjivani Superspeciality Hospital Clinical Research Department Ahmedabad
India Saviour Hospital Ahmedabad
India BGS global Hospitals Bengaluru Karnataka
India Manipal Hospital Bengaluru Karnataka
India Postgraduate Institute of Medical Education and Research Chandigarh UT
India Global Hospitals & Health City Chennai Tamil Nadu
India Sri Ramachandra Medical College and Research Chennai
India VGM Hospital Coimbatore Tamil Nadu
India Artemis Hospital Gurgaon Haryana
India Aware Global Hospital Hyderabad
India Global Hospitals Hyderabad Andhra Pradesh
India Marudhar Hospital Jaipur Rajasthan
India S.R. Kalla Memorial Gastro & General Hospital Jaipur Rajasthan
India SMS Medical College & Hospital Jaipur Rajasthan
India Lakeshore Hospital Kochi Kerala
India Institute of Post Graduate Medical Education And Research Kolkata West Bengal
India K. R. M. Hospital & Research Centre Lucknow
India KGMU Medical College Lucknow Uttar Pradesh
India M.V. Hospital and Research Centre Lucknow
India Dayanand Medical College & Hospital Ludhiana
India BYL Nair Hospital & T N Medical College Mumbai
India Midas Institute of Gastro-enterology Nagpur Maharashtra
India A.I.I.M.S. New Delhi Ansari Nagar
India Sir Ganga Ram Hospital New Delhi
India Nirmal Hospital Pvt. Ltd. Surat Gujarat
India Om Research Center, Om Surgical Center & Maternity Home Varanasi

Sponsors (1)

Lead Sponsor Collaborator
Gilead Sciences

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of adverse drug reactions (ADRs) during treatment and up to 4 weeks after discontinuation of a SOF-based regimen Up to Posttreatment Week 4
Secondary Proportion of participants with sustained virologic response (SVR) 12 weeks after discontinuation of therapy (SVR12) SVR12 is defined as HCV RNA < the lower limit of quantification (LLOQ) 12 weeks following the last dose of study drug, respectively. Posttreatment Week 12
See also
  Status Clinical Trial Phase
Completed NCT02907996 - Evaluate the Safety and Effectiveness of Sovaldi in Participants With Chronic Hepatitis C Virus (HCV) Infection in Korea
Completed NCT02207088 - Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Genotype 1-Infected Adults With Chronic Kidney Disease Phase 3
Not yet recruiting NCT02893046 - HCV Care Pathway in Ile-de-France N/A
Completed NCT01428063 - Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials Phase 2
Completed NCT01396005 - A Study to Evaluate the Pharmacokinetic Effect of SCH 503034 (Boceprevir) on Methadone or Buprenorphine/Naloxone Plasma Concentrations (P08123) Phase 1
Completed NCT01195181 - Different PEG-interferon and Ribavirin Schedules for Chronic Hepatitis C in the Real Clinical Practice. Phase 4
Completed NCT00219999 - Hepatitis C Virus and the Humoral Immune System N/A
Completed NCT02243293 - A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administration of ABT-493 and ABT-530 With and Without RBV in Subjects With Chronic Hepatitis C Virus (HCV) Genotypes 2, 3, 4, 5 or 6 Infection Phase 2/Phase 3
Completed NCT02265237 - A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir Co-administered With Ribavirin (RBV) in Adults With Genotype 4 Chronic Hepatitis C Virus (HCV) Infection and Cirrhosis (AGATE-1) Phase 3
Not yet recruiting NCT06104046 - Prevalence of Seroconversion of Hepatitis c Virus Among Children With CKD on Regular Hemodialysis
Completed NCT02604017 - A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With Genotype 1 Infection Phase 3
Withdrawn NCT00947245 - Japanese Bridging Study Conducted in the United States Phase 1
Completed NCT01713283 - Sofosbuvir Plus Ribavirin in Treatment-Naive and Treatment-Experienced Egyptian Adults With Chronic Genotype 4 Hepatitis C Virus (HCV) Infection Phase 2
Completed NCT01458535 - A Study to Evaluate ABT-450 With Ritonavir (ABT-450/r) When Given Together With ABT-267 and With and Without Ribavirin (RBV) in Treatment-Naïve Subjects With Genotype 1, 2 or 3 Chronic Hepatitis C Virus (HCV) Phase 2
Completed NCT01479881 - A Study in Healthy Participants Investigating the Effect of TMC435 on the Pharmacokinetics of Immunosuppressants Cyclosporine and Tacrolimus Phase 1
Completed NCT01193361 - Ph IIA Study (SOC +/- NS5B) Phase 2
Completed NCT01241773 - TMC435-TiDP16-C123 - A Study in Healthy Volunteers Investigating the Pharmacokinetic Interaction Between TMC435 and the Antiretroviral Agents Efavirenz and Raltegravir Phase 1
Completed NCT01006031 - Retreatment With High Doses of pegIFN Alfa-2a and Ribavirin of Previous Nonresponders HIV-coinfected Patients With Cirrhosis Due to HCV 1-4 Phase 2/Phase 3
Completed NCT00819026 - Observational Trial of Hepatitis C Virus Infected Patients on Calcineurin Inhibitors N/A
Completed NCT00382798 - Adaptive Phase I HCV Study With Nucleoside Analogue, in Combination With Interferon and Ribavirin Phase 1/Phase 2