Phase 1 Study of DS-8895a in Subjects With Advanced Solid Tumors
Launched by DAIICHI SANKYO CO., LTD. · Dec 3, 2013
Trial Information
Current as of June 18, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Advanced solid tumor that is refractory to standard treatment, or for which no standard treatment is available.
- • Eastern Cooperative Oncology Group performance status(PS) of 0 or 1
- Exclusion Criteria:
- * Have any of the following concomitant disease or had the history of having following disease within 6 months before enrollment:
- • Cardiac failure (NYHA ≥ ClassIII), myocardial infarction, cerebral infarction, unstable angina, arrhythmia requiring treatment, coronary-artery/peripheral artery bypass surgery, cerebrovascular disease, pulmonary thromboembolism, deep-vein thrombosis or clinically severe thromboembolic event, or clinically severe pulmonary disease (eg, interstitial pneumonia, pulmonary fibrosis, radiation pneumonia, drug induced pneumonia)
- • Severe or uncontrolled concomitant disease.
- • Clinically active brain metastases defined as symptomatic or requiring treatment.
About Daiichi Sankyo Co., Ltd.
Daiichi Sankyo Co., Ltd. is a global healthcare company headquartered in Tokyo, Japan, renowned for its commitment to innovative research and development in pharmaceuticals. With a rich history spanning over a century, the company focuses on delivering transformative treatments across various therapeutic areas, including oncology, cardiovascular disease, and infectious diseases. Daiichi Sankyo leverages cutting-edge science and technology to advance its drug development pipeline, emphasizing collaboration and partnership to enhance patient outcomes worldwide. Its dedication to improving global health is reflected in its extensive clinical trials, which aim to bring novel therapies to market and address unmet medical needs.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kashiwa, Chiba, Japan
Suita, Osaka, Japan
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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