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POINT Biomedical 
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POINT Biomedical is a privately held pharmaceutical company that is pursuing technologies related to imaging and drug delivery. The principal product platform is based on hollow, dual layer microspheres or bispheres. The inner shell provides physical integrity and protects the contents while the outer layer functions as the biological interface. The overall size distribution and the respective layers can be independently modified to fulfill application specific requirements. The bispheres can be filled with a gas, such as nitrogen or air, or designed to hold a variety of drugs or biotherapeutic agents, which can be released upon collapse of the bispheres under external control. The collapse of each bisphere can be monitored providing discrete feedback as to how much agent has reached the target site. Bispheres can be used to protect labile agents from premature degradation as well as alter the pharmacokinetics, metabolism and systemic toxicity of various chemotherapeutics.
Activity:
- Contract Manufacturing
- Contract Research
- Licensing & Business Development
- Manufacturing
- Research & Development
Product / Technology type(s) covered:
- Diagnostics
- Drug delivery
- Enzymes
- NCE (new chemical entities)
- Pharmaceuticals / Therapeutics
- Prescription drugs (Rx)
- Proteins
- Technology
Therapeutic targets:
- Arthritis / Rheumato
- Cancer
- Cardiovascular
- Hematology
- Oncology
- Pain
- Urology
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Company Contact
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POINT Biomedical
887 Industrial Road
94070 San Carlos
CA
United States of America
Phone: 650-596-1400
FAX: 650-596-1402
Website: http://www.pointbio.com
Send an email
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Markets Covered
a. HeadQuarter: United States of America
b. Continent(s) active:
North America
c. Countries active: United States
Corporate data:
Number of Employees: <100
Turnover:
| Amount: |
Year: |
Currency: |
| private |
2001 |
US Dollar |
Year founded: 1996
Partners / Alliances: POINT Biomedical is interested in partnering the international clinical development, product registration and commercialization of CardioSphere(tm), which is currently in Phase 3 clinical trials in the United States for myocardial perfusion in coronary disease. The NDA is expected to be filed in 2003; a CTX is in place. Multiple patents cover the underlying technology and clinical applications.
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