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Left's avatar

The question everyone should be asking about Moberg is why would a company that's too conservative to guide to capturing a substantial portion of European OTC market risk everything on a trial with a different dosing regimen. Afterall they didnt need to go as far as 8 weeks, they knew the whitening fades after around 8 weeks given they missed it in the P2.

The answer is probably that elucidating a dosing regimen to the FDA is more useful than replicating an outcome. It won't get an improved label, but if this trial failed or the efficacy was lower due to a DDR, it just puts the label europe already has into the other markets.

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griff's avatar

Great post! Tough week for the Moberg bag holders like myself but this is my favorite writeup yet.

Have you written on what tools you use company discovery, tracking potential investments, etc? I'm looking for free or low cost tools and right now I'm just at a notion doc plus Schwab's tools.

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