GSK1265744 (Cabotegravir, CAB) for Named Patient/Compassionate Use in HIV

NCT03462810 | Unknown

• 1 other identifier: 205741
• Study Type: expanded_access
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

The goal of this compassionate use program is to provide a mechanism to supply Cabotegravir, CAB on an individual named patient basis for treatment of individuals who have no available treatment alternatives and/or limited treatment options (e.g., who are unable to participate in the Phase III clinical studies or do not qualify), and are in need of new drugs to construct an effective antiviral regimen and may require the use of parenterally administered drug given underlying medical conditions. You can access ViiV's Policy on Compassionate via https://us.viivhealthcare.com/media/124424/viivs-external-policy-on-cup\_final-version\_23feb2017.pdf.

Conditions

Infection, Human Immunodeficiency Virus

Keywords

cabotegravir, CAB; GSK1265744; Individual Patient Compassionate Use; HIV

Interventions

cabotegravir, CAB DRUG

open label investigational product

Also known as: cabotegravir, CAB

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• HIV-infected patients will be eligible for treatment if ALL the following apply:
• Male or female patients aged ≥ 18 yrs
• NOTE: all female patients of reproductive potential should use every precaution to prevent pregnancy including either complete abstinence from intercourse from 2 weeks prior to administration of CAB, throughout receipt of CAB and for at least 52 weeks after discontinuation of CAB LA; or use of one of the following methods of highly reliable contraception:
• Contraceptive subdermal implant
• Intrauterine device or intrauterine system
• Combined estrogen and progestogen oral contraceptive
• Injectable progestogen
• Contraceptive vaginal ring
• Percutaneous contraceptive patches
• Male partner sterilisation with documentation of azoospermia prior to the female subject's entry into the study, and this male is the sole partner for that subject. The documentation on male sterility can come from the site personnel's: review of subject's medical records, medical examination and/or semen analysis, or medical history interview provided by her or her partner.
• These allowed methods of contraception are only effective when used consistently/correctly and in accordance with the product label. The investigator is responsible for ensuring that patients understand how to properly use these methods of contraception.
• Inability to construct a viable antiviral treatment regimen with commercially available medications;
• The patient/legal guardian or representative has given informed consent to treatment prior to administering CAB (in a manner consistent with all national requirements). The patient/legal guardian or representative has also given informed consent for the transmission of a copy of the anonymized adverse and serious adverse event (SAE) and pregnancy reports (in compliance with local regulatory authority requirements) to GSK and ViiV where allowable by local regulations, and to the country regulatory authority as required.

You may not qualify if:

• Patients will not be eligible for treatment if ANY of the following apply:
• Patient has estimated creatinine clearance \<50 mL/min via Cockcroft-Gault method;
• Females who are pregnant or women who are breastfeeding, or plan to become pregnant or breastfeed during treatment.
• Patients who have had known or suspected allergic reaction or hypersensitivity reactions to integrase inhibitors;
• Alanine aminotransferase (ALT) \>5 times the upper limit of normal (ULN)
• ALT ≥ 3 times ULN and bilirubin ≥ 1.5 times ULN (with \> 35% direct bilirubin)
• Evidence for moderate to severe hepatic impairment, grade 3-4 liver fibrosis, or cirrhosis
• Patients who are eligible for actively enrolling clinical trials involving CAB.
• Significant coagulopathy precluding chronic IM dosing
• NOTE: Patients should not be treated via the named patient/compassionate use program if they are eligible and/or able to participate in any of the Phase III clinical trials of CAB and the patient is suitable for participation in such clinical trials. In that instance (assuming consent is obtained) the patient should preferentially be enrolled into the ongoing clinical trial to allow detailed data collection. In accordance with national requirements patients should not be treated in the named patient/compassionate use program if they have responded to previous treatment with CAB in another clinical trial without review and prior approval by the VSLC.

Sponsors & Collaborators

• ViiV Healthcare: lead

MeSH Terms

Conditions

Infections; Acquired Immunodeficiency Syndrome

Interventions

cabotegravir

Condition Hierarchy (Ancestors)

HIV Infections; Blood-Borne Infections; Communicable Diseases; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; RNA Virus Infections; Virus Diseases; Slow Virus Diseases; Genital Diseases; Urogenital Diseases; Immunologic Deficiency Syndromes; Immune System Diseases

Study Officials

• GSK Clinical Trials

  ViiV Healthcare

  STUDY DIRECTOR

Central Study Contacts

US GSK Clinical Trials Call Center

CONTACT

877-379-3718; GSKClinicalSupportHD@gsk.com

Study Design

• Study Type: expanded access
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 5, 2018
• First Posted: March 13, 2018
• Last Updated: May 21, 2021

Record last verified: 2020-10