FDA Approves First Human Trials With Embryonic Stem Cells

The FDA’s approval of these first human clinical trials with Embryonic Stem Cells (ESC) signals hope for sufferers of a variety of disorders and diseases, including lymphomas, but it doesn’t tell the whole story, as some experts such as scientist Christian Drapeau believe that Adult Stem Cells (ASC) offer “greater potential with less risk” than ESCs.



Various experts have been debating the merits of ASCs and ESCs for a long time now, but one aspect of the FDA’s announcement can’t be overlooked: Less than 5% of adult cancer patients take part in clinical trials in the United States. If any clinical trial at all is going to be effective, it needs participants.



For this reason, back in October of 2007 the Leukemia & Lymphoma Society and the Cleveland Clinic Taussig Cancer Institute got together and launched the Clinical Trial Center for Hematologic Malignancies. The goal of the Center is to make participation in important clinical trials easier by overcoming common obstacles such as patient reluctance and difficult travel requirements.



For more information, either:



Call the Taussig Institute’s Cancer Answer Line at (866) 223-8100, or

Go to the Taussig Institute’s home page at http://cms.clevelandclinic.org/cancer/

More Articles

More Articles

Amazon.com is pleased to have the Lymphoma Information Network in the family of Amazon.com associates. We've agreed to ship items...

The question ought to be what are myelodysplastic syndromes (MDS), since this is a group of similar blood and bone marrow diseases that...

Merkel Cell Carcinoma (MCC) is a very rare and aggressive skin cancer that usually develops when a person is in his or her 70s. It is...

Radiation Therapy Topics

...

At some point, the Seattle biotech company Cell Therapeutics Inc (CTI) should earn an entry in the Guinness Book of World Records for utter and...

Site Beginnings

This site was started as Lymphoma Resource Page(s) in 1994. The site was designed to collect lymphoma...

Three papers appearing in the journal Blood and pointing towards a regulator-suppressor pill could offer hope to blood cancer...

The US Food and Drug Administration (FDA) has granted a third so-called Breakthrough Therapy Designation for the investigational oral...

The US Food and Drug Administration today has approved an expanded use of Imbruvica (ibrutinib) in patients with...

The U.S. Food and Drug Administration has announced that it has granted "Breakthrough Therapy Designation" for the investigational agent...

According to a new study published in the Proceedings of the National Academy of Sciences, a team from the University of California, San...

Pharmacyclics has announced that the company has submitted a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for...

New research suggests that frontline radioimmunotherapy...

Gilead Sciences has announced results of the company's Phase II study of its investigational compound idelalisib, an oral inhibitor of...

Sitemap