"I'm not persuaded that the LiGHT trial adds a lot of value. The end point was not met and no amount of post-hoc analysis (i.e. removing the non-responders from the data) can maintain the random properties of the original data. This is why the FDA is most unlikely to accept this trial as proof of efficacy. Alas another Phase III trial will be needed, this time with participants selected on the basis of anticipated efficacy (ie disease not too far advanced)."
Are you getting mixed up with the 2RT results?
Light trial was for SLT and that was a positive development for Ellex.
Valuing Ellex Laser and Ultrasound, page-3
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