Expanded Access for the Treatment of Advanced Cholangiocarcinoma With ABC294640 (Yeliva ®)

Sponsor
RedHill Biopharma Limited (Industry)
Overall Status
Available
CT.gov ID
NCT03414489
Collaborator
(none)

Study Details

Study Description

Brief Summary

This is an expanded access program (EAP) for eligible participants who do not qualify for participation in, or who are otherwise unable to access, the ongoing clinical trial ABC-108. This program is designed to provide access to ABC294640 (Yeliva ®) for treatment of cholangiocarcinoma (CCA) 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. An oncologist 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.

Study Design

Study Type:
Expanded Access
Official Title:
Expanded Access to ABC-108, A Phase IIA Study of ABC294640 in the Treatment of Patients With Advanced,Unresectable Intra-hepatic, Perihilar and Extra-Hepatic Cholangiocarcinoma

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    1. Diagnosis of cholangiocarcinoma

    2. Ineligible to participate in the ABC294640 clinical trial for the treatment of cholangiocarcinoma or geographically inaccessible to the trial.

    3. Judged by the treating oncologist to be medically suitable for treatment with ABC294640

    4. Willing and able to provide written, signed informed consent

    5. Approval by RedHill of the treating oncologist's clinical trial experience for the purpose of making ABC294640 available

    6. Regulatory approval by the appropriate jurisdiction

    Exclusion Criteria:
    1. Any medical condition that may cause treatment with ABC294640 to be potentially harmful as judged by RedHill

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • RedHill Biopharma Limited

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    RedHill Biopharma Limited
    ClinicalTrials.gov Identifier:
    NCT03414489
    Other Study ID Numbers:
    • ABC-108-EA
    First Posted:
    Jan 30, 2018
    Last Update Posted:
    Mar 16, 2022
    Last Verified:
    Mar 1, 2022

    Study Results

    No Results Posted as of Mar 16, 2022