The RESPOND Outcomes Study
NCT04090151 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 37853
Last updated 2024-04-12
Summary
The RESPOND Outcomes study is a research study around use of antiretroviral and other relevant drugs and long-term clinical outcomes in patients living with HIV. Data collected in this study will be used to answer key unanswered questions regarding treatment of people living with HIV.
Conditions
Sponsors & Collaborators
- collaborator INDUSTRY
-
ViiV Healthcare
collaborator INDUSTRY -
Rigshospitalet, Denmark
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-01-01
- Primary Completion
- 2025-12-31
- Completion
- 2025-12-31
Countries
- Australia
- Austria
- Belgium
- Denmark
- France
- Georgia
- Germany
- Italy
- Netherlands
- Spain
- Sweden
- Switzerland
- United Kingdom
Study Locations
More Related Trials
-
Immunologic and Virologic Consequences of Long-Term Highly Active Antiretroviral Therapy (HAART) in Subjects With Moderately Advanced HIV-1 Disease: A Follow-Up Study to ACTG 315
NCT00000891 ·Status: COMPLETED ·Phase: PHASE2
-
PrEPception: Expanding Assisted Reproductive Options for Serodiscordant Couples
NCT02233192 ·Status: COMPLETED
-
CD4 Cell Recovery in HIV-1 Patients Comparing 2 Treatment Regimes
NCT00966160 ·Status: COMPLETED ·Phase: PHASE3
-
Instacare - Rapid ART Initiation Among Persons With HIV and Out of Care
NCT04240691 ·Status: COMPLETED
-
Treatment Intensification for HIV Infected Patients With Multi-Drug Resistant Virus
NCT00102934 ·Status: UNKNOWN ·Phase: NA
-
Determining the Effects of Observed and Self-Administered Drug Regimens in HIV Infected Adults
NCT00608569 ·Status: COMPLETED ·Phase: NA
-
RESIST-2: 2nd-line ART for HIV-2 Infection
NCT03394196 ·Status: TERMINATED ·Phase: NA
-
Prospective Cohort of HIV/HBV-coinfected Patients in Europe
NCT04984772 ·Status: ENROLLING_BY_INVITATION
-
EuroSIDA As An External Comparator To MOTIVATE Trials
NCT01329783 ·Status: COMPLETED
-
Rapid Reinitiation of a Single Tablet Antiretroviral Therapy Using Symtuza® in HIV-1 Infected Treatment-Experienced Patients Off Therapy. (ReSTART)
NCT04388904 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Provide Continued Access to Study Drug to Children and Adolescents Who Have Completed Clinical Studies Involving Gilead HIV Treatments
NCT06337032 ·Status: RECRUITING ·Phase: PHASE4
-
Dynamics of Drug Resistance-associated Mutations in HIV-1 DNA Reverse Transcriptase Clearance During Effective Antiretroviral Therapy
NCT04448158 ·Status: COMPLETED
-
Immediate Versus Deferred Antiretroviral Therapy in HIV-infected Patients Presenting With Acute AIDS-defining Events
NCT01417949 ·Status: COMPLETED ·Phase: PHASE4
-
Accurate Staging of Immuno-virological Dynamics During Acute HIV Infection
NCT03449706 ·Status: RECRUITING
-
Lenacapavir Intensification to Disrupt HIV Reservoirs in Virologically Suppressed People With HIV Receiving Antiretroviral Therapy
NCT06819176 ·Status: RECRUITING ·Phase: PHASE1
-
Same-Day HIV Testing and Treatment Initiation to Improve Retention in Care
NCT01900080 ·Status: UNKNOWN ·Phase: NA
-
A Randomized Clinical Trial to Evaluate Solutions for the Management of Virologic Failure on TLD in Sub-Saharan Africa
NCT05373758 ·Status: RECRUITING ·Phase: NA
-
Ex Vivo Characterization and Targeting of the Latent HIV Infected Reservoir to Cure HIV
NCT05215704 ·Status: RECRUITING
-
Observational Data Analysis in EuroSIDA (MK-0518-058)
NCT01078233 ·Status: COMPLETED
-
Antiretroviral Resistance Detection by Ultrasensitive Pyrosequencing of the HIV-1 Genome and Virological Response to Antiretroviral Rescue Treatment
NCT01346878 ·Status: COMPLETED
-
Tenofovir DF (Disoproxil Fumarate) in Combination With Emtricitabine in HIV-1 Patients
NCT00106379 ·Status: COMPLETED ·Phase: PHASE4
-
A Comparison of Two Ways to Manage Anti-HIV Treatment (The SMART Study)
NCT00027352 ·Status: COMPLETED
-
Tenofovir Disoproxil Fumarate in HIV-Infected Patients Who Have Not Had Success With Other Anti-HIV Drug Combinations
NCT00011089 ·Status: UNKNOWN ·Phase: NA
-
Therapeutic Intensification Plus Immunomodulation in HIV-infected Patients
NCT01019551 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Efficacy, Safety, Participant Choice and Preference of an Oral Once-daily Regimen or a Long-acting Injectable Regimen Every Two Months for Treatment of Human Immunodeficiency Virus (HIV-1) in Adults Who Have Not Previously Taken Antiretroviral Therapy
NCT05917509 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3