Simmaron Research

@AmbrosineShitr2 We appreciate your comment. Based on decades in this disease, most doctors will only take #MECFS or #Longcovid seriously when placebo-controlled trials are successful. We have a chance to be the 1st to do that and identify biomarkers to predict who is likely to improve.

@RedefiningMECFS Drs should just prescribe a low dose to patients and monitor

We’re launching a placebo-controlled study of rapamycin for #MECFS and #LongCOVID. Early data from our Phase II trial shows promise — now we must test it under rigorous blinded conditions. Help us make it happen. Donate to support the study. simmaronresearch.com/donate #ME #Rapamycin

@Opinions_Survey We are tracking biomarkers of autophagy, activity data and patient surveys. We published results from Phase 1 in Jnl of Translational Medicine (high impact), showing correlation of these markers. That's what makes this trial unique and exciting. Jnl link: link.springer.com/article/10.118…

@RedefiningMECFS What are the biomarkers used as outcomes ? We need this info to then support the study

@AndrewG76201347 I've sent you a direct message with an email address to ask for the study proposal. Please reply to this post if you didn't get that. Thank you so much for your interest.

@RedefiningMECFS Looking forward to this, thanks. Can you please provide potential donors with a link to full info about the proposed study design so we can decide whether we think it’s worthwhile. eg for the MECFS arm, what diagnosis criteria are you using? & what validated outcomes eg FUNCAP?

@LostSock See link to our narrative of the science behind our rapamycin trial, how it is targeted to a mechanism and biomarkers, and why a placebo-controlled trial has the potential to achieve something that hasn't been done yet in #ME or #Longcovid. bit.ly/2025Simmaron

@LostSock We completely agree with your focus on underlying mechanisms. Our trial is designed around mechanisms we have published in #ME blood, our mouse model, and our Phase 1 results in Jnl Translational Medicine. Jnl: link.springer.com/article/10.118…

On behalf of Simmaron's entire research team led by @ggottschalkphd and @ProfAvikRoy, we are incredibly thankful to be producing leading research for #LongCovid, #MECFS and related IACCs. Today on Long-Covid Awareness Day, we remember those lost and see those with the lasting scars suffering. Science takes time, but we are so happy to see progress being made. Our focus remains on mechanistic clinical trials like our rapamycin clinical trial and identifying molecular pathways that are treatable. Link to rapamycin phase 1 results in Jnl of Translational Medicine: pubmed.ncbi.nlm.nih.gov/41121328/ Link to Inflammation Research paper delineating new mechanisms in #PEM: link.springer.com/article/10.100… Sign Up! simmaronresearch.com/signup

Explaining #PEM in #MECFS, new Simmaron publication identifies polarized macrophages, SIRT1, and NF-kB as actors in the inflammatory cascade that follows impaired autophagy, when ATG13 is missing. Read why this matters for #ME #Longcovid patients: simmaronresearch.salsalabs.org/musclefatiguep…

@TWestphalia @UWM @SpringerNature We published findings from phase 1 of our low dose rapamycin trial in the Journal of Translational Medicine here: link.springer.com/article/10.118…

@RedefiningMECFS @UWM @SpringerNature Pls outline treatment possibilities for patients Thks

Simmaron publication shows mechanisms of #PEM in #ME! Our new findings show a lack of ATG13 inside cells induces macrophages to take on an inflammatory role, impairing myelin in muscles, in processes aggravated by exercise. #Longcovid @UWM @SpringerNature link.springer.com/article/10.100…

TY for your reply! We published findings from phase 1 of our low dose rapamycin trial in the Journal of Translational Medicine here: link.springer.com/article/10.118…

@mecfsskeptic @SKaktus_ @UWM @SpringerNature @RenzPolster We are studying ATG13 because of our finding of phosphorylated ATG13 in the serum of a subset of #ME patients. 2022 publication here: sciencedirect.com/science/articl…

@SKaktus_ @RedefiningMECFS @UWM @SpringerNature @RenzPolster I tend to agree. The research on ATG13 is interesting but the link to ME/CFS and PEM is not so clear and seems rather speculative.

@SKaktus_ @UWM @SpringerNature @mecfsskeptic @RenzPolster We are studying ATG13 because of our finding of phosphorylated ATG13 in the serum of a subset of #ME patients. 2022 publication here: sciencedirect.com/science/articl…

@RedefiningMECFS @UWM @SpringerNature IMHO your bold claim made here don't seem sufficiently supported by your study. Just because ATG13 suppression is able to induce a PEM-like state that's no proof it's what's happening inside pwME. I'd love to hear your opinions about this :) @mecfsskeptic @RenzPolster

If you want to read the study (warning: it gets complex!) click here: link.springer.com/content/pdf/10… And if you want to #donate to support our team's work, your donation will be matched, up to $250K! Click here: simmaronresearch.com/donate

Our findings provide a biological explanation for why muscle weakness & fatigue worsen after exertion for ME/CFS patients. It's the first time PEM has been explained at a molecular level and support's our team's trial of low-dose rapamycin to help the cellular recycling process!

🧵Did you hear the news? Our team just published a landmark study detailing the chain reaction of cellular changes that occur after PEM. Our newest research helps break down how muscles and nerves can be impacted in #MECFS patients. Let's break it down 👇