Status:
COMPLETED
Safety, Tolerability, and PK of GT0918 (Proxalutamide) in Subjects With Metastatic Castrate Prostate Cancer
Lead Sponsor:
Suzhou Kintor Pharmaceutical Inc,
Conditions:
Metastatic Castrate Resistant Prostate Cancer (mCRPC)
Eligibility:
MALE
18+ years
Phase:
PHASE1
Brief Summary
This was a Phase 1, multicenter, open-label, clinical trial in adult subjects with metastatic castrate resistant prostate cancer who progressed after both hormonal therapy (abiraterone or enzalutamide...
Detailed Description
GT0918 treatment was initiated with the first dose of 50 mg/day in a cohort of 3 patients, and 6- patients per cohort for the subsequent escalated dose levels at 100 mg, 200 mg, 300 mg, 400 mg, 500 mg...
Eligibility Criteria
Inclusion
- Written informed consent obtained prior to any study-related procedure being performed.
- Subjects at least 18 years of age or older at the time of consent.
- Histologically confirmed metastatic castrate resistant cancer (mCRPC) who progressed after both hormonal therapy (abiraterone or enzalutamide) and chemotherapy (docetaxel, for example); or cannot tolerate either or both of these classes of therapies.
- Ongoing androgen deprivation therapy with a luteinizing hormone-releasing hormone (LHRH) "super-agonist" or antagonist, or bilateral orchiectomy and serum testosterone level \< 50 ng/dL (\< 0.5 ng/mL, \< 1.7 nmol/L) at screening.
- Metastatic disease documented by computed tomography (CT)/magnetic resonance imaging (MRI) or bone scan.
- Progressive disease despite ongoing androgen deprivation or chemotherapy. Progressive disease is defined by 1 or more of the following criteria:
- Subjects with a rising PSA value \> 2 ng/mL in at least 2 measurements, at least 1 week apart. If the confirmatory PSA value is less than the screening PSA value, then an additional test for the rising PSA is required to document progression.
- Subjects with measurable disease, progression defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria.
- Subjects with metastatic bone disease, progression defined by 2 or more new lesions in a radionuclide bone scan.
- ECOG performance status of 0-2 (dose escalation phase); ECOG performance status of 0-1 (expansion phase).
- Screening blood counts of the following:
- Absolute neutrophil count ≥ 1500/μL
- Platelets ≥ 100,000/μL
- Hemoglobin \> 9 g/dL
- Screening chemistry values of the following:
- Alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 2.5 × upper limit of the normal reference range (ULN)
- Total bilirubin ≤ 2 × ULN
- Creatinine ≤ 1.5 × ULN
- Albumin \> 2.8 g/dL.
- At screening, life expectancy of at least 3 months.
- Subjects whose partners are women of childbearing potential (WOCBP) must use an adequate method of birth control while on study drug and at least for 3 weeks after discontinuation of study drug.
- Subject is willing and able to comply with all protocol required visits and assessments.
Exclusion
- Subjects with life expectancy less than 3 months.
- Discontinuation of bicalutamide or nilutamide less than 6 weeks, and other antiandrogens less than 4 weeks, abiraterone less than 3 weeks, prior to the start of study medication.
- Prior chemotherapy, radiation, sipuleucel-T or other experimental immunotherapy less than 4 weeks prior to the start of study medication.
- Prior chemotherapies more than 2 lines (Phase II part only) .
- Ongoing acute treatment-related toxicity associated with a previous therapy greater than grade 1 except for grade 2 alopecia or neuropathy.
- History of impaired adrenal gland function (eg, Addison's disease, Cushing's syndrome).
- Known gastrointestinal disease or condition that affects the absorption of GT0918.
- History of congestive heart failure New York Heart Association (NYHA) class III or IV or uncontrolled hypertension at screening.
- History or family history of long QT syndrome.
- History of other malignancy within the previous 3 years, except basal cell or squamous cell carcinoma, or non-muscle invasive bladder cancer.
- Use of systemic glucocorticoid (eg, prednisone, dexamethasone) within 14 days prior to the start of study medication.
- Co-administration of CYP3A4 ligands that serve as substrates or induce or inhibit the enzyme.
- Prior use of any herbal products known to decrease PSA levels (eg, PC-SPES or saw palmetto) within 30 days prior to the start of study medication.
- Major surgery within 30 days prior to the start of study medication.
- Blood transfusion (including blood products) within 1 week of screening.
- Serious persistent infection within 14 days prior to the start of study medication.
- Serious concurrent medical condition including CNS disorders.
- Previous history of difficulty swallowing capsules.
- Known hypersensitivity to GT0918 or its excipients.
- Any condition that, in the opinion of the investigator, would impair the subject's ability to comply with study procedures.
Key Trial Info
Start Date :
February 10 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 15 2020
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT02826772
Start Date
February 10 2016
End Date
February 15 2020
Last Update
March 17 2020
Active Locations (6)
Enter a location and click search to find clinical trials sorted by distance.
1
Chesapeake Urology Research Associates
Towson, Maryland, United States, 21204
2
G U Research Network
Omaha, Nebraska, United States, 68130
3
Comprehensive Cancer Centers of Nevada
Las Vegas, Nevada, United States, 89169
4
Rutgers University
New Brunswick, New Jersey, United States, 08901