Skip to content

Post-market Study for the Safety and Effectiveness of E/C/F/TAF tablet (Genvoya) and F/TAF tablet (Descovy) in the treatment of Patients with Human Immunodeficiency Virus 1 (HIV-1) infection in China

Post-market Study for the Safety and Effectiveness of E/C/F/TAF tablet (Genvoya) and F/TAF tablet (Descovy) in the treatment of Patients with Human Immunodeficiency Virus 1 (HIV-1) infection in China

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000028825
Enrollment
Unknown
Registered
2020-01-05
Start date
2020-01-10
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV-1

Interventions

Case series:NA

Sponsors

Shanghai Public Health Clinical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients (aged 12 years and older with body weights of at least 35 kg) who are Chinese and living in China; 2. Patients with HIV-1 infection eligible for treatment with E/C/F/TAF tablet (Genvoya) or F/TAF tablet (Descovy) as indicated in the approved prescribing information; 3. Patients who have been informed of all pertinent aspects of the study and have voluntarily signed an informed consent form (patients under 18 years of age must also have signed consent from either parents or a legally authorized representative (i.e., a legal guardian) who has been informed of all pertinent aspects of the study)."

Exclusion criteria

Exclusion criteria: 1. Patients treated with E/C/F/TAF tablet (Genvoya) or F/TAF tablet (Descovy) outside of the approved prescribing information in China; 2. Concurrent participation in a clinical trial of HIV treatment (except trials not testing investigational medicinal products); 3. Patients who have a contraindication as indicated under prescribing information: 4. Patients planning on leaving the country for an extended period during the study period; 5. Patients deemed by the investigator to be unlikely to maintain regular medical follow-up through at least 48 weeks".

Design outcomes

Primary

MeasureTime frame
Occurrence of adverse events;Treatment success (Proportion of patients achieving virologic response at 48 weeks after the start of treatment);

Countries

China

Contacts

Public ContactAlan Zhao

Shanghai Public Health Clinical Center

alan.zhao@gilead.com+86 18618178535

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026