Triple Negative Breast Cancer (TNBC) Clinical Trial
Official title:
Expanded Access to Veliparib
NCT number | NCT03123211 |
Other study ID # | C16-468 |
Secondary ID | C19-918C20-120 |
Status | No longer available |
Phase | |
First received | |
Last updated |
Verified date | May 2022 |
Source | AbbVie |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Expanded Access |
This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to veliparib prior to approval by the local regulatory agency. Availability will depend on territory eligibility. 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. EAP is also available for other indications where there is reasonable scientific basis for efficacy.
Status | No longer available |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - The patient has relapsed/refractory disease and exhausted all standard treatments. - The patient has documented Breast Cancer (BRCA), BRCA associated RING domain (BARD), or Partner and Localizer of Breast Cancer (PALB) or other acceptable deoxyribonucleic acid (DNA) mutations. Exclusion Criteria: - The patient is eligible for a Poly Adenosine diphosphate ribose polymerase (PARP) inhibitor clinical trial. - The patient has previously received a PARP inhibitor for the same disease. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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AbbVie |
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