Ovarian Cancer Clinical Trial
PLX2853 as a Single Agent in Advanced Gynecological Malignancies and in Combination With Carboplatin in Platinum-Resistant Epithelial Ovarian Cancer
The purpose of this research study is to evaluate safety, pharmacokinetics, pharmacodynamics and preliminary efficacy of the investigational drug PLX2853 in Advanced Gynecological Malignancies with a Known ARID1A Mutation and PLX2853/Carboplatin Combination Therapy in Platinum-Resistant Epithelial Ovarian Cancer.
Age ≥18 years at the time of signing informed consent
Histologically or cytologically confirmed diagnosis of 1 of the following, and must have measurable disease per RECIST v1.1:
Phase 2a (PLX2853 monotherapy): Any advanced gynecological malignancy (cervical, vaginal, vulvar, uterine, ovarian, fallopian tube, or primary peritoneal) with a known ARID1A mutation, that is intolerant to or refractory to all standard therapy known to confer clinical benefit.
Phase 1b and Phase 2a (PLX2853 + carboplatin combination):
Platinum-resistant EOC (including fallopian tube or primary peritoneal cancer).
Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 1
Adequate organ function as demonstrated by laboratory values.
Women of child bearing potential (defined as any female who has experienced menarche and who has not undergone successful surgical sterilization or is not postmenopausal) must have a negative serum pregnancy test within 7 days prior to taking the first dose of study drug and, if sexually active, must agree to use a highly effective method of contraception (a contraception method with a failure rate <1% per year) and 1 additional barrier method from the time of the negative pregnancy test to 90 days after the last dose of study drug. Women of non-child bearing potential may be included if they are either surgically sterile or have been postmenopausal for ≥1 year.
Except as specified above for organ function, all drug-related toxicity from previous cancer therapy must be resolved (to Grade ≤1 or baseline per National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 [NCI CTCAE v5.0]) prior to study treatment administration (Grade 2: alopecia, hot flashes, decreased libido, or neuropathy is allowed).
Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements
Prior exposure to a bromodomain inhibitor
Ongoing systemic infection requiring treatment with antibiotic, antiviral, or antifungal treatment
Autoimmune hemolytic anemia or autoimmune thrombocytopenia
Presence of symptomatic or uncontrolled central nervous system or leptomeningeal metastases
Red blood cell or platelet transfusion within 14 days of Screening blood draw
Known or suspected allergy to the investigational agent or any agent given in association with this study
Use of biotin (i.e., Vitamin B7) or supplements containing biotin higher than the daily adequate intake of 30 μg (NIH-ODS 2020).
Use of strong inhibitors and inducers of CYP3A4 and 2C8
Clinically significant cardiac disease
Inability to take oral medication or significant nausea and vomiting, malabsorption, or significant small bowel resection that, in the opinion of the Investigator, would preclude adequate absorption
Non-healing wound, ulcer, or bone fracture
Infection with HIV-1 or HIV-2. Exception: subjects with well-controlled HIV (e.g., CD4 >350/mm3 and undetectable viral load) are eligible.
Current active liver disease from any cause, including hepatitis A (hepatitis A virus immunoglobulin M positive), hepatitis B (hepatitis B virus [HBV] surface antigen positive), or hepatitis C (hepatitis C virus [HCV] antibody positive, confirmed by HCV ribonucleic acid).
Active known second malignancy with the exception of any of the following:
Adequately treated basal cell carcinoma, squamous cell carcinoma of the skin, or in situ cervical cancer
Adequately treated Stage I cancer from which the subject is currently in remission and has been in remission for ≥2 years
Any other cancer from which the subject has been disease-free for ≥3 years
Major surgery or significant traumatic injury within 28 days prior to Cycle 1 Day 1
Hospitalization for subacute bowel obstruction within 28 days prior to Cycle 1 Day 1
Receipt of anti-cancer therapy prior to Cycle 1 Day 1:
Chemotherapy, radiation therapy, or small molecule anti-cancer therapy for the treatment of cancer within 14 days or 5 half-lives (whichever is shorter) of Cycle 1 Day 1
Immune therapy or other biologic therapy (e.g., monoclonal antibodies, antibody-drug conjugates) for the treatment of cancer within 21 days or 5 half-lives (whichever is shorter) of Cycle 1 Day 1 Subjects can receive a stable dose of bisphosphonates for bone metastases, before and during the study as long as these were started at least 28 days prior to treatment with study drug.
Subject is participating in any other therapeutic clinical study (observational or registry studies are allowed).
Subjects who are pregnant or breast-feeding
Presence of any other medical, psychological, familial, sociological, or geographic condition potentially hampering compliance with the study protocol or would interfere with the study endpoints or the subject's ability to participate.
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There are 8 Locations for this study
Chicago Illinois, 05841, United States
Boston Massachusetts, 02114, United States
New York New York, 10065, United States
Oklahoma City Oklahoma, 73104, United States
Nashville Tennessee, 37203, United States
Charlottesville Virginia, 22908, United States
Fairfax Virginia, 22031, United States
Seattle Washington, 98109, United States
Toronto Ontario, , Canada
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