Fostemsavir Compassionate Use Named Patient Program for the Treatment of Human Immunodeficiency Virus 1 (HIV-1)
NCT04233047 · Status: AVAILABLE · Type: EXPANDED_ACCESS
Last updated 2025-05-13
Summary
Compassionate use access to fostemsavir (GSK3684934, formerly BMS-663068) for the treatment of HIV infection in individuals with multidrug resistant HIV-1 infection who are experiencing virologic failure and are unable to comprise a suppressive regimen with currently available antiretrovirals.
Direct inquires to the ViiV Compassionate Use Portal via https://viiv-cu-portal.idea-point.com/
Conditions
- HIV Infections
Interventions
- DRUG
-
Fostemsavir
Fostemsavir 600 mg extended release tablets, administered 600 mg twice daily, will be supplied for compassionate use for the identified individual patient.
Sponsors & Collaborators
-
ViiV Healthcare
lead INDUSTRY
Principal Investigators
-
GSK Clinical Trials · ViiV Healthcare
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
More Related Trials
-
Study of Enfuvirtide in HIV-Positive Subjects
NCT00086710 ·Status: COMPLETED ·Phase: PHASE1
-
Treatment Intensification for HIV Infected Patients With Multi-Drug Resistant Virus
NCT00102934 ·Status: UNKNOWN ·Phase: NA
-
BOSS Study: A Study of Fuzeon Using the Needle-Free Biojector 2000 in Patients With HIV-1 Infection
NCT00337701 ·Status: COMPLETED ·Phase: PHASE4
-
Vicriviroc (SCH 417690) in Combination Treatment With Optimized ART Regimen in Experienced Participants (VICTOR-E1) (MK-7690-020/P03672)
NCT00243230 ·Status: COMPLETED ·Phase: PHASE2
-
Vicriviroc in HIV(R5/X4)-Treatment Experienced Subjects (Study P05057AM5)(COMPLETED)
NCT00551330 ·Status: COMPLETED ·Phase: PHASE2
-
Tenofovir Disoproxil Fumarate in HIV-Infected Patients Who Have Not Had Success With Other Anti-HIV Drug Combinations
NCT00011089 ·Status: UNKNOWN ·Phase: NA
-
Accelerated ART Initiation for PWHIV Who Are Out of Care
NCT06374758 ·Status: RECRUITING ·Phase: PHASE4
-
An Expanded Access Protocol for a Single Subject Who Has Completed 24-Weeks of Treatment in PR0140_CD02 Study
NCT02759042 ·Status: NO_LONGER_AVAILABLE
-
Research In Viral Eradication of HIV Reservoirs
NCT02336074 ·Status: COMPLETED ·Phase: PHASE2
-
Changes in Immunologic Parameters Following the Addition of Fostemsavir in Virologically Suppressed Immunologic Non-responders Living With HIV-the RECOVER Study
NCT05220358 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
A Study of Enfuvirtide (Fuzeon) in Patients With Advanced Human Immunodeficiency Virus-1 (HIV-1) Infection
NCT02569502 ·Status: COMPLETED ·Phase: PHASE4
-
Prospective Evaluation Among Patients Infected by HIV 1 in Virological Failure Owing to Lack of Compliance, of the Benefit in Terms of Compliance of an Optimised Antiretroviral Treatment With Enfuvirtide (Fuzeon) Associated With Two Active Molecules
NCT00937729 ·Status: TERMINATED
-
Emtricitabine/Tenofovir Alafenamide as Salvage ART
NCT02556333 ·Status: TERMINATED ·Phase: PHASE2
-
A Pilot,Raltegravir Versus NRTIs as a Backbone Switched From a Stable Boosted PI Regimen
NCT00749580 ·Status: COMPLETED ·Phase: NA
-
Implementation of Onsite, Rapid ART Initiation Among People Who Inject Drugs Living With HIV at Syringe Services Program
NCT04650269 ·Status: COMPLETED ·Phase: PHASE4
-
Pilot Study Evaluating Interruption of Enfuvirtide (Fuzeon, T20) in Patients With Enfuvirtide Resistance
NCT00187551 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of VICRIVIROC in HIV-Infected Treatment-Naïve Subjects (Study P04875)
NCT00551018 ·Status: COMPLETED ·Phase: PHASE2
-
Early Fast-Track Versus Standard Care for Persons With HIV Initiating TLD
NCT04311944 ·Status: UNKNOWN ·Phase: NA
-
Lenacapavir Intensification to Disrupt HIV Reservoirs in Virologically Suppressed People With HIV Receiving Antiretroviral Therapy
NCT06819176 ·Status: RECRUITING ·Phase: PHASE1
-
A Study of Fuzeon (Enfuvirtide) With an Integrase Inhibitor Plus Optimized Background in Treatment-Experienced HIV-1 Infected Patients
NCT00488059 ·Status: TERMINATED ·Phase: PHASE4
-
Vicriviroc in HIV-Treatment Experienced Subjects (Study P04889AM8)(COMPLETED)
NCT00474370 ·Status: COMPLETED ·Phase: PHASE3
-
GW640385 Plus Ritonavir And NRTIs For 48 Weeks In HIV-1 Infected Adults
NCT00257621 ·Status: COMPLETED ·Phase: PHASE2
-
Vicriviroc, a CCR5 Inhibitor, Added to an Optimized Antiretroviral Therapy for Previously Treated HIV (VICTOR-E2) (Study P04285
NCT00243568 ·Status: WITHDRAWN ·Phase: PHASE3
-
A Study Comparing the Efficacy and Safety of Once-Daily Fuzeon (Enfuvirtide) Dosing Versus the Currently Recommended Twice-Daily Dosing in Human Immunodeficiency Virus-Type 1 (HIV-1) Infected Patients
NCT00089492 ·Status: COMPLETED ·Phase: PHASE2
-
QUALITE Study - A Study of Fuzeon (Enfuvirtide) in Treatment-Experienced Patients With Human Immunodeficiency Virus-1 (HIV-1) Infection
NCT00232908 ·Status: COMPLETED ·Phase: PHASE4