Published in Gene Therapy Weekly, April 5th, 2001
The IND application was based on positive pre-clinical toxicology results for GTI-2501, an antisense compound, which demonstrated that the drug was well tolerated in studies using animals. The findings also suggested that GTI-2501 could be used safely in clinical trials with human patients, at concentration levels that exceed potential therapeutic doses.
"The FDA approval of our IND application allows Lorus to...
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Source: Gene Therapy Weekly (2001-04-05)
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