The Wall Street Journal (12/14, B2, Rockoff,
Subscription Publication) reports Marlborough, Massachusetts-based Advanced
Cell Technology Inc. (ACT) says it is ready to undergo the steps it needs to
take towards obtaining approval from the Food and Drug Administration to launch
what would be first human study involving stem cells that were developed by
reprogramming adult cells to return to an embryonic-like condition. The Journal
notes that ACT's Chief Scientific Officer Robert Lanza said that the company
presently has the capability to produce enough platelets for the initial
clinical studies. However, the FDA declined to comment on the pending trials
because it is prohibited under Federal law from discussing potential therapies
under development. The Journal adds that earlier this year, the two researchers
who designed the mature cell reprogramming process, which would cancel the need
to use embryos, were awarded a Nobel Prize for their work.
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