Annovis Phase 3 Trial - has anyone partic... - Cure Parkinson's

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Annovis Phase 3 Trial - has anyone participated?

curepdnow profile image
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If anyone has participated in Annovis P3 Trial I'd love to hear your thoughts on it. Thanks in advance for sharing.

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curepdnow
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jimcaster profile image
jimcaster

I participated at the University of Kansas in Kansas City. I may have been on the placebo, but I did not notice any effects, either positive or negative. Personally, I don't think 6 months is enough time for a Parkinson's trial. The symptoms progress so slowly that it's difficult to know whether a particular drug is having much of an effect in such a short amount of time. At the time of the trial I was in contact with several others who participated. A couple reported good results, but the vast majority felt little or no effect like me.

PDTom profile image
PDTom in reply to jimcaster

it doesn't sound as if buntanetap will manage to become a drug.

How do you rate it?

Do you think it will continue after the phase 3 trial?

The results should be coming in the next few weeks...

For me, buntanetap was a beacon of hope. I'm still doing well, but it would be a drug without side effects.

jimcaster profile image
jimcaster in reply to PDTom

I'm skeptical. Somehow, positive results were observed in a short amount of time in the phase 2 trial, but I think Annovis Bio is better at attracting investors than it is at curing Parkinson's. Just my opinion...

Pixelpixie profile image
Pixelpixie

I participated too. Saw no results

NextStage profile image
NextStage

I was in the trial. I don't know if I had the placebo or not. Besides subjectively feeling like I was improving, I also got some objective data. I would periodically do a righthand typing test (all words only use letters that the right hand should be typing) before taking my morning meds. During the first two months taking the trial drug I steadily improved my word count until it matched my left hand, which is unaffected. After the trial stop it has held steady. However, I am a believer in the "No Silver Bullet" and try many things. A bit after stopping the trial I started doing Intermittent Fasting. I also increased usage my vibrating gloves following PD Buzzboards design. Finally, in the last several weeks I have started sprouting Broccoli seeds and eating the sprouts every day. So, I'm not sure how much of the continuation of the effect after stopping the drug could be attributed to a permanent (semi-permanent?) change in my condition due to the drug versus other interventions having a positive effect.

I copied this reply from another post about this trial.

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