Don't forget Techinvest that there will likely be some flexibility with this....in terms of:
* A potential RMAT designation.
* Timing of a 2nd trial (eg. post market approval)
* Real world data post approval versus a conventional P3 tiral.
* Tasly's heart failure trial in China may negate the need for MSB (or future partner) to conduct a 2nd P3 trial.
Tech please try and be a little more balanced with future posting.
Ann: P3 Trial of MSB's Cell Therapy in CHF Completes Recruitment, page-22
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