clinical trial to evaluate the safety and efficacy of a drug under investigation called AVB S6 500 in combination with Paclitaxel in women with ovarian cancer which comes back after a platinum therapy.
- Conditions
- Platinum-Resistant Recurrent Ovarian CancerMedDRA version: 21.1Level: PTClassification code 10066697Term: Ovarian cancer recurrentSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2021-000293-28-CZ
- Lead Sponsor
- Aravive, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Female
- Target Recruitment
- 400
1.Histologically confirmed and documented recurrent ovarian, fallopian tube, or peritoneal cancer. Only patients with high-grade serous adenocarcinoma histology are eligible.
2.Aged 18 years or older
3.Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 to 1
4.Ability to understand the nature of this clinical study and willingness to give written informed consent, comply with scheduled visits, the treatment plan, laboratory tests, and follow up visits
5.Platinum resistant disease (defined as progression within =6?months from completion of most recent platinum-containing regimen and calculated from the date of the last administered dose of platinum therapy). Subject may have been treated with additional regimen(s) subsequent to determination of platinum resistance.
6.Available archived tumor tissue (a paraffin-embedded tissue block with sufficient tumor tissue for biomarker testing or unstained slides with sufficient tumor tissue may be substituted) or if archived tissue is not available, a fresh tumor biopsy is required.
7.Radiologic imaging with a computerized tomography (CT) scan or magnetic resonance imaging (MRI) (if cannot tolerate a CT scan) within 21 days of randomization. (If a site can document the CT performed as part of the positron emission tomography [PET]-CT is of identical diagnostic quality to a diagnostic CT [with IV and oral contrast], then the CT portion of a PET-CT can be used.)
8.Received at least 1 but not more than 4 prior therapy regimens since ovarian cancer diagnosis.
Note: maintenance therapy OR hormonal therapies should not be counted as a separate therapy.
9.Ovarian cancer that is measurable according to RECIST v1.1
10.Normal gastrointestinal (GI) function. This includes no GI obstruction, NG tube, or bleeding or signs/symptoms thereof within 3?months prior to randomization. If nausea or vomiting is present due to prior treatment, symptoms must be recovered to Grade 1 or less. Subjects with a history of abdominal fistula will be considered eligible if the fistula was surgically repaired or has healed, there has been no evidence of fistula for at least 6?months, and the subject is deemed to be at low risk of recurrent fistula.
11.Life expectancy >3 months
12.Negative serum pregnancy test within 7 days of randomization for females of childbearing potential (premenopausal and not surgically sterilized)
13.Adequate bone marrow function:
a.Absolute neutrophil count =1500/µL
b.Platelet count =100,000/ µL
c.Hemoglobin =9.0 g/dL
14.Adequate hepatic function:
a.Total bilirubin =1.5×upper limit of normal (ULN)
b.Aspartate aminotransferase (AST) =3.0×ULN*
c.Alanine aminotransferase (ALT) =3.0×ULN*
*Unless liver metastases are present, in which case AST/ALT must be =5×ULN
15.Adequate renal function as determined by calculated or measured creatinine clearance =30?mL/min (using Cockcroft-Gault equation).
16.International normalized ratio (INR) =1.5 and activated partial thromboplastin time (aPTT) =1.5 ULN for subjects not on anticoagulation treatment. If subjects are on anticoagulation treatment, the corresponding laboratory values should be in therapeutic range for the respective agent.
17.Full recovery from all recent surgery on date of randomization; at least 1 week must have elapsed from the time of a minor surgery (port placement at any time is acceptable); from the date of randomization at least 21 days must have elapsed from the time of a major surgery.
1.Tumors in the breast or bone
2.Untreated central nervous system (CNS) metastases (surgery and/or radiotherapy). Subjects requiring corticosteroid therapy for the management of their treated CNS metastases may not be on >10 mg/day prednisone or equivalent OR have demonstrated signs or symptoms of neurologic instability for 28 days or less prior to randomization.
3.Primary platinum-refractory disease (defined as progression during or within 4 weeks after completion of the first platinum regimen)
4.Is being treated with concurrent anticancer therapy or other interventional treatments administered for their underlying ovarian cancer.
5.Received prior therapy with PAC in the recurrent setting
6.Clinically significant cardiac disease history including the following:
a.cardiac arrhythmia uncontrolled on medication
b.unstable angina or clinically and/or electrocardiographically documented myocardial infarction within 6 months before randomization
c.clinically significant valvular disease
d.uncontrolled congestive heart failure
e.QT (QTc) prolongation >470 msec
f.clinically significant pericardial effusion.
7.History of a prior malignancy that was active (not indolent) within the previous 3 years, except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, endometrial stage 1 cancer, or carcinoma in situ of the cervix or breast
8.History of or present CNS disease unrelated to cancer, unless adequately treated with standard medical therapy (eg, uncontrolled seizures)
9.Nonhealing wound, ulcer, or bone fracture
10.Paracentesis for ascites within 3 months prior to the first dose of Study Treatment or has clinically significant active pleural effusion, anasarca, or other evidence of third spacing
11.Serious active infection requiring IV antibiotics and/or hospitalization within 7 days of randomization.
12.Known severe hypersensitivity to any of the study drugs or excipients, including history of allergic, anaphylactic, or other severe hypersensitivity reactions to fusion proteins, products containing Cremophor EL (eg, cyclosporin for injection concentrate and teniposide for injection concentrate), or known hypersensitivity or allergy to Chinese hamster ovary cell products
13.History of or evidence of any other medical conditions (such as psychiatric illness, etc.), therapy, physical examination or laboratory findings that may interfere with the subject’s participation for the full duration of the Study Treatment, affect subject compliance, place the subject at high risk from treatment-related complications, confound the results of the study, or is not in the best interest of the subject to participate
14.Known previous or current human immune deficiency (HIV) syndrome, hepatitis?B, or hepatitis C, or any other known active viral illness such as COVID-19
15.Ever participated in a study with AVB-S6-500
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method