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Pre-approval Single-patient Expanded Access for Talazoparib (PF-06944076)

Primary Purpose

Metastatic Castration-Resistant Prostate Cancer

Status
Available
Phase
Locations
Study Type
Expanded Access
Intervention
Talazoparib
Sponsored by
Pfizer
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Metastatic Castration-Resistant Prostate Cancer focused on measuring Prostate Cancer, metastatic* Castration-Resistant Prostate Cancer (mCRPC), enzalutamide, combination therapy, first-line mCRPC, metastatic (M1)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)Male

Talazoparib is not intended for monotherapy. Talazoparib is intended for combination use with enzalutamide in first-line metastatic (M1) Castration-Resistant Prostate Cancer (mCRPC) only. Must be a newly diagnosed mCRPC patient who has not yet received 1st line therapy (1st generation Androgen Receptor (AR)-inhibitors do not count). Must have not received 2nd generation AR-inhibitors (enzalutamide, apalutamide, darolutamide), a Poly [ADP-ribose] polymerase (PARP)-inhibitor, cyclophosphamide, or mitoxantrone as prior treatments in any prostate cancer disease setting. Previous abiraterone and/or docetaxel for hormone-sensitive disease (CSPC) is allowed (patient eligible). Patients with identified need for use of potent P-glycoprotein (P-gp) inducer drugs within 7 days of onset/under duration of talazoparib plus enzalutamide treatment are at risk of drug-drug interactions (DDIs) and are therefore ineligible. Additional eligibility criteria may be required.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    December 6, 2022
    Last Updated
    September 19, 2023
    Sponsor
    Pfizer
    Collaborators
    In Expanded Access, treating physicians are the Sponsors
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05650476
    Brief Title
    Pre-approval Single-patient Expanded Access for Talazoparib (PF-06944076)
    Study Type
    Expanded Access

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Available
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Pfizer
    Collaborators
    In Expanded Access, treating physicians are the Sponsors

    4. Oversight

    5. Study Description

    Brief Summary
    Provide pre-approval single-patient Expanded Access (Compassionate Use) of talazoparib for patients with metastatic castration-resistant prostate cancer.
    Detailed Description
    Expanded Access requests from treating physicians may be submitted at www.pfizercares.com; availability will depend on location/country.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Metastatic Castration-Resistant Prostate Cancer
    Keywords
    Prostate Cancer, metastatic* Castration-Resistant Prostate Cancer (mCRPC), enzalutamide, combination therapy, first-line mCRPC, metastatic (M1)

    7. Study Design

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Talazoparib
    Intervention Description
    capsules

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Eligibility Criteria
    Talazoparib is not intended for monotherapy. Talazoparib is intended for combination use with enzalutamide in first-line metastatic (M1) Castration-Resistant Prostate Cancer (mCRPC) only. Must be a newly diagnosed mCRPC patient who has not yet received 1st line therapy (1st generation Androgen Receptor (AR)-inhibitors do not count). Must have not received 2nd generation AR-inhibitors (enzalutamide, apalutamide, darolutamide), a Poly [ADP-ribose] polymerase (PARP)-inhibitor, cyclophosphamide, or mitoxantrone as prior treatments in any prostate cancer disease setting. Previous abiraterone and/or docetaxel for hormone-sensitive disease (CSPC) is allowed (patient eligible). Patients with identified need for use of potent P-glycoprotein (P-gp) inducer drugs within 7 days of onset/under duration of talazoparib plus enzalutamide treatment are at risk of drug-drug interactions (DDIs) and are therefore ineligible. Additional eligibility criteria may be required.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Pfizer Cares
    Email
    PfizerCares@pfizer.com

    12. IPD Sharing Statement

    Learn more about this trial

    Pre-approval Single-patient Expanded Access for Talazoparib (PF-06944076)

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