Open-Label Extension and Safety Study of Talazoparib

Pfizer

Status and phase

Completed

Phase 2

Conditions

Cancer

Treatments

Drug: Talazoparib

Study type

Interventional

Funder types

Industry

Identifiers

C3441010 (Other Identifier)

2016-001972-31 (EudraCT Number)

MDV3800-13

Details and patient eligibility

About

This is a single-arm, open-label, extended treatment, safety study in patients treated with talazoparib in qualifying studies.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
Female patients of childbearing potential must have a negative pregnancy test before the first dose of talazoparib and must agree to use a highly effective birth control method from the time of the first dose of talazoparib through 45 days after the last dose.
Male patients must use a condom when having sex with a pregnant woman or with a woman of childbearing potential from the time of the first dose of talazoparib through 105 days after the last dose. Contraception should be considered for a nonpregnant female partner of childbearing potential.
Female patients may not be breastfeeding at the first dose of talazoparib and must not breastfeed during study participation through 45 days after the last dose of talazoparib.

Exclusion criteria

Permanently discontinued from any Medivation sponsored study with talazoparib alone or in combination with another agent.
Received an antineoplastic therapy or investigational agent after treatment with talazoparib in the originating protocol.
Has a clinically significant cardiovascular, dermatologic, endocrine, gastrointestinal, hematologic, infectious, metabolic, neurologic, psychologic, or pulmonary disorder or any other condition, including excessive alcohol or drug abuse, or secondary malignancy, that may interfere with study participation in the opinion of the investigator.
Diagnosis of myelodysplastic syndrome (MDS).