We’re excited to return after a short break and who better to bring us back than these 4 powerhouse women: @gwenpetersen7, Leah Stavenhagen, @shellymckenna, & Sally Stewart.
Join us for Project ALS Research Live on Tues, June 1, 1pm ET.
Register here: https://t.co/CQNHdWhWRw
Project ALS mourns the passing of the multi-Tony-nominated actress and singer Rebecca Luker from ALS. Rebecca was diagnosed with ALS out of nowhere last year—and immediately rallied her Broadway community, leading the charge for ALS research and advocacy. She changed the world.
Through the generous support of the Wasserman family and Project ALS, the lab of Dr. Alejandro Chavez is pursuing an ambitious project to develop broad acting ALS therapeutics.
Read our newest blog post to learn more: https://t.co/cW1OfGMsyc
Thanks @RebeccaJLuker for making a huge difference in the path to a cure for #ALS and your courage in telling your story. Wishing you strength and love. @ProjectALSorg
For the record: ALS is still barbaric, the lack of meaningful treatments is still unacceptable, and we will fight with incredible leaders like @sandymorris333 until Jenifer’s words no longer resonate.
Project ALS is proud to support this work, led by Drs. Valeria Gerbino and Tom Maniatis (Columbia), through our collaborative effort to understand the role of autophagy in ALS. Through the @projectalsCORE we are applying these important findings to therapeutic discovery for ALS.
The ALS community is all too familiar with earth-shattering health crises like COVID-19, and Project ALS remains committed to moving our lead drug candidate, Prosetin, to clinical trial as quickly as possible. Watch the full update from our team here:
https://t.co/DvpJLF3dzk
Today our Panther Family came together in support of Eric Stevens and @stevens_nation and raised $43,000 for #ProjectALS. We must #AxeALS for all 30,000 Americans living with ALS 💙🙏🏻
@als_out Hi Eric, we know this is a little late but someone from Project ALS would be happy to come and speak to the group - we are not far away! You know how to reach us if you'd like to set it up.
We'll be working with Dr. Elyaman to develop: (1) more useful biomarkers for ALS—i.e. more disease-specific than what's currently validated—and (2) targeted treatments that hit ALS-specific inflammatory/immune pathways.
We know that neurodegenerative diseases like ALS, Alzheimer's, Parkinson’s, & even MS have common features, like neuroinflammation and immune system dysfunction.
THE CORE is excited to work with Wassim Elyaman, PhD—an expert on neuroinflammation and immunity in Alzheimer's and MS—to better understand the specifics of what's happening to these mechanisms in ALS.
This is interesting. What therapies might we have today if we had a conditional approval path yrs ago? Could confirmatory studies actually find responder groups? Would today's ALS therapies actually be less expensive had there been confirmatory studies? https://t.co/3pWv0kXBVk
@alsadvocacy In theory, drugs approved via AA require a Ph 4 confirmatory trial to stay on the market. Looks like it doesn't always play out that way in practice: https://t.co/iidmXrbNFB
@myalsworld The Nurown Ph 3 trial should be very helpful in starting to answer that question for MCP-1...but we need to be measuring many promising biomarkers across ALL ALS clinical trials so we can really ID the best markers of the disease.
@myalsworld Hi—great question! We should host a livestream about this topic, as it's nuanced. 30,000ft answer: yes, we will use MCP-1 & more (like NF-L)! But those are not direct markers of ALS—we have more work to do to validate that a change in MCP-1=an impact on a person's ALS.