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Expanded Access to Glecaprevir/ Pibrentasvir

Expanded Access to Glecaprevir/ Pibrentasvir

Status
APPROVED_FOR_MARKETING
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT03123965
Enrollment
Unknown
Registered
2017-04-21
Start date
Unknown
Completion date
Unknown
Last updated
2020-01-18

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

Conditions

Hepatitis C Virus Infection

Keywords

Special Access Scheme, Expanded Access, Pre-approval Access, Compassionate Use, Special Access Program, Named Patient Basis

Brief summary

This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to glecaprevir/ pibrentasvir prior to approval by the local regulatory agency. Availability will depend on territory eligibility. Participating sites will be added as they apply for and are approved for the EAP. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.

Interventions

DRUGglecaprevir

Glecaprevir will be administered orally.

DRUGpibrentasvir

Pibrentasvir will be administered orally.

Sponsors

AbbVie
Lead SponsorINDUSTRY

Eligibility

Age
18 Years to No maximum
Healthy volunteers
No

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026