Extension study for HER2 amplified advanced solid tumors (JUPITER ES)
- Conditions
- Solid tumorsHER2, solid tumorD009369
- Registration Number
- JPRN-jRCTs031220444
- Lead Sponsor
- Ikeda Sadakatsu
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 3
(1) Patients enrolled in the Phase II study and continuing on study treatment at the time of obtaining consent for this study.
(2) Women of child-bearing potential and partners of child-bearing potentail must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) for the duration of study participation, and for 28 weeks following completion of study therapy.
(3) Patients signed informed consent form.
(1) Patients who participated in clinical studies other than the Phase II trials within 4 weeks prior to obtaining consent for this study.
(2) Patients who have a clinically significant medical condition that makes participation in this study inadvisable or makes compliance with the requirements of this study difficult.
(3) Any other patients who are regarded as inappropriate for inclusion in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method