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Triple Negative Breast Neoplasms clinical trials

View clinical trials related to Triple Negative Breast Neoplasms.

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NCT ID: NCT03123211 No longer available - Clinical trials for Triple Negative Breast Cancer (TNBC)

Expanded Access to Veliparib

Start date: n/a
Phase:
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.

NCT ID: NCT03067935 No longer available - Clinical trials for Metastatic gpNMB Expressing Triple Negative Breast Cancer

Individual Patient Expanded Access-Glembatumumab Vedotin

Start date: n/a
Phase:
Study type: Expanded Access

Celldex endeavors to make investigational products available to patients with life-threatening diseases who have exhausted other treatment options and where there is a reasonable expectation of benefit over risk. Requests for expanded access to glembatumumab vedotin in patients with gpNMB expressing triple negative breast cancer will be considered.

NCT ID: NCT02985658 No longer available - Clinical trials for Triple-Negative Breast Cancer

Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer

Start date: n/a
Phase:
Study type: Expanded Access

This is an expanded access protocol to allow continued maintenance therapy with ABT-888 (veliparib) for three patients with metastatic triple negative breast cancer who are currently receiving the investigational product in association with clinical trial participation. Additionally, the protocol will enroll up to 7 new patients with metastatic BRCA associated or triple negative breast cancer to allow for additional access to veliparib monotherapy, or at the investigator's discretion, veliparib in combination with cisplatin and/or vinorelbine.