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Orplatna cancer drug under FDA advisory panel srutiny

With prostate cancer being one of the most deadly forms for men to suffer from, the introduction of more pharmaceutical drugs that specifically treat prostate cancer are sure to increase.

One of the first such subjects is GPC Biotech AG's Orplatna, which is getting a reprieve by and FDA advisory panel. The panel suggested to the FDA that more evidence (like clinical trials, I suppose) is needed before Orplatna is approved for use in the U.S. for prostate cancer patients.

The panel suggested that data needed to be shown that showed whether or not Orplatna-using patients lived longer than others who received a placebo. In other words, hard data on survival rate needs to be shown, and GPC Biotech AG's response is that it will take at least a year for that to become available.

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