A clinical trial to evaluate a new medicine (Zolbetuximab) for the treatment of pancreatic cancer
- Conditions
- First Line Treatment in Subjects with Claudin 18.2 (CLDN18.2) Positive, Metastatic Pancreatic AdenocarcinomaTherapeutic area: Diseases [C] - Cancer [C04]MedDRA version: 20.0 Level: LLT Classification code 10033599 Term: Pancreatic adenocarcinoma metastatic System Organ Class: 100000004864
- Registration Number
- EUCTR2018-002551-15-ES
- Lead Sponsor
- Astellas Pharma Global Development, Inc. (APGD)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Not specified
- Target Recruitment
- 141
1. Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written informed consent and privacy language as per national regulations (e.g., Health Insurance Portability and Accountability Act Authorization for United States sites) must be obtained from the subject or legally authorized representative prior to any study related procedures (including withdrawal of prohibited medication, if applicable).
2. Subject is considered an adult according to local regulation at the time of signing informed consent.
3. Subject agrees not to participate in another interventional study while
receiving study drug in present study.
4. A female subject is eligible to participate if she is not pregnant or lactating and at least 1 of the following conditions applies:
? Not a woman of childbearing potential (WOCBP) as defined in the Protocol.
OR
? WOCBP who agrees to follow the contraceptive guidance as defined in the Protocol throughout the treatment period and for at least 6 months after the final study drug administration.
5. Female subject must agree not to breastfeed starting at screening and
throughout the study period, and for 6 months after the final study drug administration.
6. Female subject must not donate ova starting at screening and throughout the study period, and for 6 months after the final study drug administration.
7. A male subject with female partner(s) of child-bearing potential must agree to use contraception as detailed in the Protocol during the treatment period and for at least 6 months after the final study drug administration.
8. A male subject must not donate sperm during the treatment period and for at least 6 months after the final study drug administration.
9. Male subject with a pregnant or breastfeeding partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy or time partner is breastfeeding throughout the study period and for 6 months after the final study drug administration.
Disease Specific Criteria
10. Subject has histologically or cytologically confirmed adenocarcinoma of pancreas.
11. Subjects must have metastatic pancreatic cancer that has not been previously treated with chemotherapy.
? Prior treatment with 5-FU or GEM administered as a radiation sensitizer during
and up to 4 weeks after radiation therapy is allowed (if there is lingering toxicity,
then the sponsor should be consulted).
? If a subject received therapy in the adjuvant setting, tumor recurrence or disease progression must have occurred at least 6 months after completing the
last dose of adjuvant therapy.
12. Subject has a measurable lesion(s) on at least 1 metastatic site based on RECIST 1.1 within 28 days prior to the first dose of study treatment. For subjects
with only 1 measureable lesion and prior radiotherapy, the lesion must be outside the field of prior radiotherapy or must have documented progression following radiation therapy.
13. Subject's tumor sample has CLDN18.2 expression in = 75% of tumor cells
demonstrating moderate to strong membranous staining as determined by cent
Subject will be excluded from participation if any of the following apply:
Prohibited Treatment or Therapies
1. Subject has received other investigational treatment within 28 days
prior to screening.
2. Subject has received radiotherapy for metastatic pancreatic
adenocarcinoma within 28 days prior to the first dose of study treatment. Subject who received palliative radiotherapy to peripheral bone metastases = 14 days prior to first dose of study treatment and has recovered from all acute toxicities is eligible.
3. Subject has received systemic immunosuppressive therapy, including systemic
corticosteroids within 14 days prior to first dose of study treatment. Subject using a physiologic replacement dose of hydrocortisone or its equivalent (defined as up to 30 mg per day of hydrocortisone or up to 10 mg per day of prednisone) or a single dose of systemic corticosteriods is eligible.
Medical History or Concurrent Disease
4. Subject has prior severe allergic reaction or intolerance to known ingredients of zolbetuximab or other monoclonal antibody, including humanized or chimeric
antibodies.
5. Subject has known immediate or delayed hypersensitivity, intolerance or
contraindication to any component of study treatment.
6. Subject has a known history of a positive test for human immunodeficiency virus infection or known active Hepatitis B (positive HBs antigen [Ag]) or
Hepatitis C infection. For subjects who are negative for HBs Ag, but Hepatitis B core antibody positive, a Hepatitis B virus DNA test will be performed and if positive, the subject will be excluded. Subjects with positive serology but negative Hepatitis C virus RNA test results are eligible.
7. Subject has a history of interstitial pneumonia or pulmonary fibrosis.
8. Subject has pleural effusion or ascites = Grade 3 per CTCAE v 4.0.
9. Subject has an active autoimmune disease that has required systemic treatment in the past 2 years.
10. Subject has active infection requiring systemic therapy that has not completely resolved per investigator judgment within 14 days prior to first dose of study treatment.
11. Subject has significant cardiovascular disease, including:
? Congestive heart failure (defined as New York Heart Association Class
III or IV), myocardial infarction, unstable angina, coronary angioplasty, coronary stenting, coronary artery bypass graft, cerebrovascular accident or hypertensive
crisis within 6 months prior to administration of first dose of study treatment;
? History of clinically significant ventricular arrhythmias (i.e., sustained ventricular tachycardia, ventricular fibrillation or Torsades de Pointes);
? QTc interval > 450 msec for male subjects; QTc interval > 470 msec for female
subjects;
? Cardiac arrhythmias requiring anti-arrhythmic medications (Subjects with rate
controlled atrial fibrillation for > 1 month prior to first dose of study treatment
are eligible.)
12. Subject has known active or treated central nervous system metastases and/or carcinomatous meningitis.
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