PU-H71 With Nab-paclitaxel (Abraxane) in Metastatic Breast Cancer

Metastatic Breast Cancer Clinical Trial

Official title:

A Phase 1b Study of PU-H71 With Nab-paclitaxel (Abraxane) in Patients With HER2-Negative Metastatic Breast Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03166085
• Other study ID #: 17-093
• Status: Completed
• Phase: Phase 1
• Start date: May 23, 2017
• Est. completion date: December 14, 2021

Study information

• Verified date: December 2021
• Source: Memorial Sloan Kettering Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to decide the best dose of the study drug, PU-H71, that can be given in combination with the standard chemotherapy drug, nab-paclitaxel (Abraxane).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: December 14, 2021
• Est. primary completion date: December 14, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age 18 years or older

• Signed informed consent

• Patients must have histologically confirmed HER2-negative breast cancer (defined as IHC 0 or 1+ and/or fluorescence in situ hybridization [FISH] < 2.0), that is metastatic in stage

• For estrogen receptor (ER)-positive breast cancer, patients must be considered refractory to endocrine therapy, having received and progressed through at least one prior line of endocrine therapy, or are intolerant of endocrine therapy

• All patients must have progressed on at least one line of cytotoxic therapy for metastatic disease

• Patients must have evidence of progressive disease

• Measurable or non-measurable disease as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).

• Hematologic parameters: white blood cell (WBC) count of = 3000/ul, absolute neutrophil count (ANC) = 1500/ul, platelets = 100,000/ul, hemoglobin = 9.0 g/dl

• Non-hematologic parameters: bilirubin = 1.5 mg/dl, AST/ALT = 3.0 x upper limit of normal (ULN) (= 5.0 x ULN if liver metastases are involved)

• Serum creatinine < 1.5 xULN or CrCl > 40 mL/min (measured or calculated using the Cockcroft-Gault formula)

• An Eastern Cooperative Oncology Group performance status of 0-2

• Life expectancy of 3 months or more as assessed by the investigator

• Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures

• Negative ß-human chorionic gonadotropin (hCG) pregnancy test for premenopausal women of reproductive capacity (those who are biologically capable of having children) and for women less than 12 months after menopause.

• Women of childbearing potential must agree and commit to the use of a highly effective method of contraception. Men must agree and commit to use a barrier method of contraception while on treatment and for 3 months after last dose of investigational products.

Exclusion Criteria:

• Symptomatic brain or CNS metastases. Previously treated and stable CNS disease is allowed.

• Any of the following for the treatment of cancer within 2 weeks of first study treatment: chemotherapy, immunotherapy, experimental therapy, or biologic therapy.

• Radiation therapy (other than palliative radiation to bony metastases) as cancer therapy within 4 weeks prior to initiation of study treatment

• Any major surgical procedure within 4 weeks of first study treatment

• Prior treatment with Abraxane

• Active liver disease, including viral or other hepatitis, or cirrhosis

• Pregnancy or lactation

• Other active infections aside from hepatitis

• Any other significant medical condition not under control, including any acute coronary syndrome within the past 6 months.

• Patients with a permanent pacemaker

• Patients with a QTc > 480 ms in the baseline EKG

• Surgery, radiotherapy, or lesion ablative procedure to the only area of measurable/evaluable disease

• Peripheral neuropathy of grade = 2 per NCI CTCAE, Version 4.0, at the time of or within 3 weeks prior to the first study therapy

• Other medications, or severe acute/chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results in the judgment of the investigator

• History of an invasive second primary malignancy diagnosed within the previous 3 years, except for appropriately treated stage I endometrial or cervical carcinoma or prostate carcinoma treated surgically, and non-melanoma skin cancer.

Related Conditions & MeSH terms

• Breast Neoplasms
• Metastatic Breast Cancer

Intervention

Drug:
• PU-H71
PU-H71 will be given as an intravenous infusion on Day 1 of a 21 day cycle
• Nab-paclitaxel
nab-paclitaxel will be administered at a dose of 260mg/m2 intravenously on Day 1

Locations

Country	Name	City	State
United States	Memorial Sloan Kettering Cancer Center	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center	Samus Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD)	The MTD will be the dose level at which 0/6 or 1/6 patients experience excessive toxicity with the next higher dose having at least 2/3 or 2/6 patients experiencing excessive toxicity. This means that if only 3 patients have been treated at a particular dose level and none of them had excessive toxicity, another 3 patients will be treated to verify that no more than 1 out of 6 patients had excessive toxicity.	1 year

External Links

•   Memorial Sloan Kettering Cancer Center